Abstract
Current evidence suggests that amniotic fluid volume (AFV) is actively regulated by vesicular transport of amniotic fluid outward across the amnion and into the underlying fetal vasculature in the placenta. Our objective was to determine whether gene expression profiles of potential stimulators, inhibitors, and mediators of vesicular transport are altered in response to changes in intramembranous absorption (IMA) rate. Samples of ovine amnion and chorion were obtained from fetal sheep with normal, experimentally reduced or increased AFVs and IMA rates. Amnion and chorion levels of target mRNAs were determined by RT‐qPCR. In the amnion, caveolin‐1 and flotillin‐1 mRNA levels were unchanged during alterations in IMA rate. However, levels of both were significantly higher in amnion than in chorion. Tubulin‐α mRNA levels in the amnion but not in chorion were reduced when IMA rate decreased, and amnion levels correlated positively with IMA rate (P < 0.05). Dynamin‐2 mRNA levels were not altered by experimental conditions. Vascular endothelial growth factor (VEGF 164 and VEGF 164b) mRNA levels increased during both increases and decreases in IMA rate, whereas soluble Flt‐1 levels did not change. Neither HIF‐1α nor PBEF mRNA levels in the amnion were correlated with VEGF 164 expression levels and were not related to IMA rate. Collectively, our findings suggest that changes in amnion microtubule expression may be important in the regulation of transcellular vesicular transport of amniotic fluid and thus modulate IMA rate. Further, our results are consistent with the concept that the amnion is the rate‐limiting layer for amniotic fluid transport.
Keywords: Amniotic fluid volume, tubulin, vascular endothelial growth factor, vesicular transport
Introduction
The mechanisms that regulate amniotic fluid volume (AFV) remain not well understood even though disorders of AFV occur in 5–10% of human pregnancies and are associated with increased morbidity and mortality (Locatelli et al. 2004; Morris et al. 2014; Shrem et al. 2016; Khan and Donnelly 2017). Over the past 25 years, a growing body of evidence based on experimental animal studies has shown that the primary determinant of AFV is the rate of transport of amniotic fluid outward across the amnion into the underlying fetal vasculature that perfuses the fetal surface of the placenta (Gilbert and Brace 1989; Gilbert et al. 1997; Brace et al. 2004, 2014b; Adams et al. 2005; Brace and Cheung 2014). This process, termed intramembranous absorption (IMA), is dependent upon the transport characteristics of the amnion (Adams et al. 2005; Brace and Cheung 2011). A series of studies has shown that, although water and smaller solutes move passively in both directions across the intramembranous pathway, the majority of IMA is mediated by unidirectional vesicular transport of water and solutes (Adams et al. 2005; Gesteland et al. 2009; Brace et al. 2014a). This conclusion is supported by findings from electron and fluorescence microscopy studies of the amnion that observed pinocytotic vesicles with apparent transport characteristics (King 1993; Shandley et al. 1997; Shen et al. 2008). Further, when IMA rate was experimentally altered, only the vesicular component of IMA changed while the passive components were unaltered (Gesteland et al. 2009; Brace et al. 2014a).
Currently, little is known of the cellular and molecular processes that mediate vesicular transcytosis of amniotic fluid across the amnion. In a variety of mammalian cells including endothelial, epithelial and cancer cells, transport vesicles including caveolae, lipid rafts and clathrin‐coated vesicles have been described (Li et al. 2013; Bitsikas et al. 2014; Kirchhausen et al. 2014). Our recent study, using fluorescence super‐resolution microscopy, has identified caveolar and clathrin‐coated vesicles in human amnion that exhibited uptake and transport behavior consistent with intramembranous absorption of amniotic fluid (Sharshiner et al. 2017). However, the mechanisms that mediate this vesicular uptake and transport are unclear. The dependence of transport rate on abundance of vesicles, rate of internalization of vesicles from the plasma membrane, or changes in microfilamental structures along which vesicles are transported has not been explored. Further, although experimental studies demonstrated the presence of powerful stimulator(s) and inhibitor(s) of IMA in amniotic fluid (Anderson et al. 2013; Brace et al. 2014b), the identity of these regulators has yet to be determined and the associated signaling mediators have not been identified (Cheung et al. 2014). Finally, even though the amnion has been proposed as the rate‐limiting barrier, the involvement of the chorion in mediating changes in IMA has not been investigated and it is not clear whether changes in molecular profiles in the chorion parallel those in the amnion.
In order to address these gaps in understanding, this study conducted in chronically catheterized ovine fetuses was designed with three aims. Our first aim was to gain insight into the trans‐amnion transport processes. To do this, we examined several potential factors that may be involved in regulating vesicle number and transport in the amnion. For exploring the types of transport vesicles, we selected caveolin‐1 as a marker for caveolar vesicles (Gross et al. 2017), and flotillin‐1, an integral membrane protein associated with planar lipid rafts (Salzer and Prohaska 2001). These principal components are known to be widely expressed in many cell types to regulate vesicle transport functions (Head et al. 1838; Chen et al. 2002). To study vesicle internalization and release, we selected the vesicle fission effector dynamin‐2 that mediates vesicle separation from the plasma membrane (Henley et al. 1998). For investigating transcellular vesicle movement specifically via the microtubule pathway, we focused on tubulin‐α, an essential constituent of microtubules (Heald and Nogales 2002).
The second aim of this study was to explore whether vascular endothelial growth factor (VEGF) participated in the cell signaling pathways that regulated IMA rate and determine whether known regulators of VEGF may function as the purported stimulator(s) and inhibitor(s) of IMA. Our early studies in fetal sheep demonstrated that VEGF mRNA levels in the amnion were elevated whenever IMA rate was experimentally increased (Cheung 2004). In other studies of endothelial and epithelial cells, exogenous VEGF has been shown to increase permeability by inducing caveolar transport (Feng et al. 1999; Chen et al. 2002; Harvey et al. 2016). The proposed mechanism was a VEGF‐ mediated caveolar endocytosis. Further, we previously reported that VEGF activated caveolin‐1 phosphorylation in ovine amnion cells (Cheung et al. 2010). However, caveolin‐1 is known to negatively regulate nitric oxide synthase activity (Liu et al. 2017) and caveolin‐1 mRNA levels were reduced in fetal sheep when IMA was elevated during fetal hypoxia (Cheung and Brace 2008). These opposing actions of caveolin‐1 and its interactions with VEGF raised the need to explore the relationships among VEGF, caveolin‐1 and IMA rate in the amnion. In order to determine whether known activators of VEGF would modulate IMA rate through VEGF expression, we selected two factors: hypoxia inducible factor‐1α (HIF‐1α) which activates VEGF transcription (Forsythe et al. 1996), and pre‐β cell colony‐enhancing factor (PBEF) which up‐regulates VEGF gene expression and increases VEGF receptor activities in amnion cells (Astern et al. 2013). In addition, we tested two potential inhibitors of VEGF activities: soluble fms‐like tyrosine kinase‐1 (sFlt‐1, sVEGF‐R1) (Kendall and Thomas 1993) which binds VEGF thus reduces VEGF bioavailability, and VEGF164b, a VEGF164 isoform formed by alternate splicing of the VEGF gene, that antagonizes the VEGF receptor‐mediated downstream signaling pathways (Nowak et al. 2008; Ngo et al. 2014).
The third aim of this study was to determine whether experimentally induced changes in gene expression profile of vesicular transport components in the amnion would also occur in the chorion. Although the amnion has been recognized as the rate‐limiting barrier for IMA, the chorion is in intimate contact with the outer surface of the amnion and is vascularized by fetal blood vessels in the ovine model (Brace et al. 1992). As such, the chorion could potentially participate in the regulation of intramembranous transport of amniotic fluid.
In order to address the above 3 aims, we determined the gene expression pattern of the selected mediators of IMA in the amnion and chorion of ovine fetuses subjected to experimentally induced modifications in IMA rate and AFV. The hypotheses tested were that experimentally produced changes in IMA rate would be associated with (1) alterations in expression of vesicle‐associated mediators and microtubule components that facilitate transcellular vesicular transport; (2) changes in VEGF mRNA levels that are consistent with the induced changes in IMA rate and AFV, and that the VEGF regulators tested could function as the proposed stimulator(s) and inhibitor(s) of IMA; and (3) changes in gene expression profiles that are specific to the amnion but not the chorion, supporting the concept that amnion is the rate‐limiting layer for amniotic fluid transport.
Materials and Methods
Ovine tissues
We utilized amnion and chorion tissues of late gestation ovine fetuses obtained from recent studies in chronically catheterized fetal sheep. The experimental protocols were described elsewhere (Cheung et al. 2016). Tissues were collected 2 days after initiating one of four different experimental conditions: control, urine drainage without fluid replacement, urine drainage with isovolumic fluid replacement (lactated Ringer's solution), and continuous intra‐amniotic fluid infusion (2 L/day of lactated Ringer's solution). AFV was measured at the beginning and end of the 2‐day experimental period and IMA rate, measured as a mean over the 2 days, was determined from the change in AFV and the time integrated amniotic inflows and outflows (Robertson et al. 2009; Anderson et al. 2013). The experimental design was based on our observations that, compared to control conditions, urine drainage reduces IMA and AFV, urine replacement reduces IMA and increases AFV, and intra‐amniotic fluid infusion increases both IMA and AFV (Anderson et al. 2013; Brace et al. 2014a).
Quantitative reverse transcription‐polymerase chain reaction (RT‐qPCR)
Total RNA was extracted from amnion and chorion tissues using an RNeasy Kit (Qiagen, Inc., Valencia, CA). The relative quantities of target mRNA in the tissues were determined by RT‐qPCR for caveolin‐1, flotillin‐1, dynamin‐2, tubulin‐α, VEGF164, and VEGF164b, sFlt‐1, PBEF and HIF‐1α. The methodologies were similar to those recently described (Cheung et al. 2016). Single strand cDNA synthesis from total RNA (2 μg) was carried out using MultiScribe reverse transcriptase and random primers in the presence of RNase inhibitor (Applied Biosystems, Life Technologies, Foster City, CA). Sample cDNA (25 ng/sample) was amplified with ovine‐specific primers and probes custom designed using Primer Express® Software v3.0 (Applied Biosystems, Thermo Fisher Scientific) (Table 1). The amplified sequences were validated by sequencing and alignment to the consensus ovine sequences. For the amplification reaction, TaqMan Gene Expression Assays (Applied Biosystems, Thermo Fisher Scientific) were used in a ViiA7 Real‐Time PCR System (Applied Biosystems). Two endogenous references, 18S ribosomal RNA and ovine RPLP0 mRNA, were used as house‐keeping genes. For each endogenous reference and target gene, a standard curve was incorporated in order to yield accurate quantitative values needed for comparative analysis. The mean of triplicate C T values interpolated from the respective standard curves were corrected for amplification efficiency. The ΔC T for each of the target mRNAs was calculated by subtracting the geometric mean C T of the 2 endogenous reference genes. The fold change (2−∆∆CT) of target gene relative to the respective ∆C T in amnion under control condition (the latter is used as the calibrator) was determined by the Comparative C T method (Schmittgen and Livak 2008), where ∆C T denotes the target C T value referenced to the house‐keeping genes and ∆∆C T the difference from ∆C T in control amnion.
Table 1.
Gene | Primer/probe | Nucleotide sequence | Amplicon size |
---|---|---|---|
VEGF164 | Forward | GGCGAGGCAGCTTGAGTTAA | 75 |
Reverse | CACCGCCTCGGCTTGTC | ||
Probe | 6FAMCGAACGTACTTGCAGATGMGBNFQ | ||
VEGF164b | Forward | AACACAGACTCGCGTTGCAA | 63 |
Reverse | GGTGAGACGTCTGCAAGTACGTT | ||
Probe | 6FAMCGAGGCAGCTTGAGMGBNFQ | ||
sFlt‐1 | Forward | TGCCGAGCTAGGAACATATACACA | 103 |
Reverse | AGATCCGAGAGAAAACAGCCTTT | ||
Probe | 6FAMAAGAAATCCTCCAGAAGAAMGBNFQ | ||
Caveolin‐1 | Forward | TGTGATTGCAGAACCAGAAGGA | 61 |
Reverse | GGTGAAGCTGGCCTTCCA | ||
Probe | 6FAMCACACAGTTTCGATGGCMGBNFQ | ||
Flotillin‐1 | Forward | CACAGAGGGACTACGAGCTGAA | 58 |
Reverse | CGGCGCGTGTTGACTTC | ||
Probe | 6FAMAAGGCCGCATACGACMGBNFQ | ||
Dynamin‐2 | Forward | CGGCTGAGAGGAAGTTTTTCC | 61 |
Reverse | CCCATGCGGTCCGCTAT | ||
Probe | 6FAMACCCAGCCTACCGGCMGBNFQ | ||
Tubulin‐α | Forward | ACGTGGTTCCCAAAGATGTCA | 66 |
Reverse | GCTGCGCTTGGTCTTGATG | ||
Probe | 6FAMTGCTGCCATTGCCMGBNFQ | ||
HIf‐1α | Forward | CCATGCCCCAGATTCAAGAT | 59 |
Reverse | ACTTTGTCTGGTGCTTCCATCA | ||
Probe | 6FAMAGCCAGCTAGTCCTTMGBNFQ | ||
PBEF | Forward | TGATCCCAACAAAAGGTCCAA | 63 |
Reverse | AAATTTCCTGCTGGTGTCCTATG | ||
Probe | 6FAMAAGGGCCGATTATCMGBNFQ |
Statistics and data presentation
Data are presented as means ± SE. Paired and unpaired t‐tests as well as parametric one and two factor ANOVAs were used for statistical comparisons. For the two factor ANOVAs, the interaction term indicates whether changes in the two tissues differed with experimental condition. Post hoc testing utilized Fisher's least significant difference if the null hypothesis was rejected. Bivariate (Brace 1977) and multivariate least squares regression were used to explore relationships between and among mRNA levels and IMA rate. Pearson's correlation coefficient (r) was used to determine the closeness of fit to a linear relationship of the data. Logarithmic transformation was used to normalize variances prior to statistical testing as needed. The relative amounts of mRNA were analyzed after logarithmic transformation; this method yielded identical statistical results and graphs as analyses using ΔΔC T values or ΔC T values with the exception that the scale on the vertical axis changed. A probability value P ≤ 0.05 was considered significant. Regressions and correlations that were not statistically significant are not shown.
Results
Experimental values of IMA rate and AFV as well as their ranges are given in Table 2. Urine drainage reduced IMA rate and AFV below control levels while intra‐amniotic fluid infusion increased both above control (P < 0.05, ANOVA). The decrease in mean IMA rate and increase in AFV following urine replacement with lactated Ringer's solution were not statistically significant.
Table 2.
Experimental conditions | Intramembranous absorption rate (mL/day) | Amniotic fluid volume (mL) | ||
---|---|---|---|---|
Mean ± SE | Range | Mean ± SE | Range | |
Control | 667 ± 159 | 395–1075 | 1110 ± 125 | 865–1449 |
Urine drainage | 101 ± 120* | −190–394 | 300 ± 77* | 128–437 |
Urine replacement | 515 ± 29 | 453–567 | 1449 ± 220 | 864–1862 |
Intra‐amniotic infusionb | 1366 ± 274* | 813–1945 | 3351 ± 365* | 2351–4101 |
*P < 0.05 compared to respective control.
Data from Cheung et al. (2016).
Lactated Ringer's solution infused at 2 L/day (1.39 mL/min).
Caveolin‐1 mRNA levels in the amnion did not change significantly with experimental condition (Figure 1) and were unrelated to IMA rate for all four experimental groups combined (n = 16, P = 0.99). In the chorion, caveolin‐1 mRNA levels were not correlated with IMA rate (P = 0.61). Caveolin‐1 mRNA levels in the amnion were much higher than those in the chorion for all experimental groups (P < 0.0001, Fig. 1).
Neither in the amnion nor in chorion did flotillin‐1 mRNA levels change significantly from control during experimental conditions (Fig. 1). Flotillin‐1 mRNA levels in the amnion were higher than in the chorion (P = 0.0023) but were not related to IMA rate (P = 0.42). In contrast, chorion flotillin‐1 mRNA levels were negatively correlated with IMA rate (n = 16, r = −0.59, P < 0.05).
In the amnion and chorion, dynamin‐2 mRNA levels were unchanged under experimental conditions compared to control (Fig. 2). Even though the ANOVA suggested significant differences among groups, post hoc testing found no significance between individual groups. Dynamin‐2 levels in both amnion (P = 0.73) and chorion (P = 0.46) were not correlated with IMA rate.
Tubulin‐α mRNA levels in the amnion were significantly reduced during urine drainage and urine replacement (ANOVA, P < 0.05) but did not change with intra‐amniotic fluid infusion (Fig. 2). In the chorion, tubulin‐α levels were not significantly altered by experimental conditions. Tubulin‐α mRNA levels in the amnion were positively correlated with IMA rate (n = 16, r = 0.546, P = 0.029, Fig. 3), while levels in the chorion were not (P = 0.17).
The VEGF164 mRNA levels in the amnion were elevated during intra‐amniotic fluid infusion compared to control (ANOVA, P < 0.05). However, levels were also elevated during urine drainage and urine replacement (Fig. 4). In the chorion, VEGF164 mRNA levels were significantly higher than in the amnion under all conditions, averaging 4.00 ± 0.59 times (P < 0.0001). However, chorionic levels did not vary with experimental condition. Neither amnion (P = 0.87) nor chorion (P = 0.23) VEGF164 levels correlated with IMA rate. The relationship between VEGF164 and caveolin‐1 was determined and found to correlate negatively in the amnion (r = −0.52, P = <0.05) but not in the chorion (P = 0.08).
The changes in VEGF164b mRNA levels essentially paralleled those of VEGF164 under all experimental conditions (Fig. 4). However, VEGF164b levels were significantly lower. The VEGF164b mRNA abundance averaged 2.60 ± 0.05% and 2.98 ± 0.06% (n = 16, P < 0.0001) of VEGF164 mRNA levels in the amnion and chorion, respectively. In both tissues, there were no correlations between VEGF164b mRNA levels and IMA rate (P = 0.85 for amnion, P = 0.17 for chorion). For the combined amnion and chorion values (n = 32), VEGF164b levels were highly correlated with that of VEGF164 (r = 0.993, P < 0.0001).
Amnion mRNA levels of sFlt‐1 were higher than those in the chorion (P < 0.0001, Fig. 5). The levels in both tissues did not change with experimental conditions and were not correlated with IMA rate (P = 0.58 for amnion, P = 0.74 for chorion).
PBEF mRNA levels were not altered with experimental conditions in either amnion or chorion (Fig. 6). There was no significant correlation between PBEF and VEGF164 mRNA levels in the amnion (P = 0.48) or chorion (P = 0.95); and neither amnion (P = 0.39) nor chorion (P = 0.63) PBEF mRNA levels correlated with IMA rate. Hypoxia inducible factor ‐1α mRNA levels in the amnion and chorion under the four experimental conditions are shown in Figure 6. HIF‐1α mRNA levels were elevated in both tissues during intra‐amniotic infusion (ANOVA, P < 0.001). Neither amnion nor chorion HIF‐1α mRNA levels correlated with VEGF164 (P = 0.47 for amnion, P = 0.13 for chorion), but amnion HIF‐1α levels positively correlated with IMA rate (n = 16, r = 0.57, P < 0.05) while chorion levels did not (P = 0.23).
When multivariate regression analysis of mRNA quantities for all target genes in the amnion and the chorion were performed, IMA rate was positively correlated with tubulin‐α in the amnion and negatively with flotillin‐1 in the chorion (R = 0.72, P < 0.01).
Discussion
Previous studies have provided substantial evidence supporting the concept that IMA is mediated primarily by unidirectional vesicular transport of amniotic fluid outward across the amnion (Brace et al. 2014a). In this study, we explored the cellular and molecular mechanisms that potentially underlie changes in vesicular transport rate that would lead to large changes in IMA as induced experimentally (Gesteland et al. 2009; Brace and Cheung 2014).
In the amnion, the absence of change in expression levels of caveolin‐1, a structural component of caveolae (Galbiati et al. 1998), and flotillin‐1, an integral membrane protein of lipid rafts (Salzer and Prohaska 2001), together with the lack of correlation with IMA rate suggests that vesicle number might not be altered by experimental conditions. This implies that vesicular transport may not be dependent on the number of caveolae or lipid rafts in the amnion. In the chorion, the negative correlation between IMA rate and flotillin‐1 expression may suggest a response to changes in transport. However, our previous studies (Adams et al. 2005) indicated that transfer across the chorion was rapid rather than rate‐limiting under all experimental conditions and thus most likely not a site of regulation.
It is important to note that both caveolin‐1 and flotillin‐1 expression levels in the amnion were much higher than in the chorion suggesting that vesicles may be more abundant in the amnion consistent with a unique transport function of this tissue.
During endocytosis, dynamin‐2 participates in the cleavage and release of membrane invaginations to form intracellular vesicles (Henley et al. 1998). Although amnion dynamin‐2 mRNA levels tended to be lowered in all experimental groups compared to control, the lack of correlation with IMA rate does not support a major role for dynamin‐2 in mediating the experimentally induced changes in IMA.
Tubulins are structural components of microtubules that facilitate intracellular vesicle trafficking (Heald and Nogales 2002). The present finding that amnion tubulin‐α mRNA levels decreased when IMA rate was reduced during urine drainage and urine replacement suggests that a decline in structural integrity/number of microtubules may contribute to the reduction in transport rate under these conditions. This premise is supported by the positive correlation between amnion tubulin‐α mRNA levels and IMA rate by both bivariate and multivariate regression analyses. However, the lack of increase in tubulin‐α mRNA during intra‐amniotic infusion when IMA rate was elevated suggests additional factors may be involved. Importantly, since tubulin‐α level in the chorion was not affected by experimental conditions nor related to IMA rate, it appears that the response observed in the amnion was specific to the amnion, further supporting the concept that tubulin may play an important role in mediating intramembranous transport across the amnion and ultimately regulate AFV.
As anticipated (Cheung 2004), VEGF164 mRNA levels in the amnion were elevated as IMA rate increased. However, rather than being reduced during reductions in IMA rate as expected, VEGF164 mRNA levels were significantly increased. This suggests that factors other than VEGF may be involved in regulating IMA rate under experimental conditions. The mRNA levels of VEGF164b were detectable in ovine amnion; however, the levels were low representing only 3% of VEGF164 mRNA levels. Additionally, the changes in amnion VEGF164b mRNA levels paralleled those of VEGF164 in response to experimental conditions instead of being inversed and were not related to IMA rate. This indicates not only that the changes in expression levels of the 2 isoforms could be the consequence of a common mechanism rather than a negative relationship but also that VEGF164b would not be participating in regulation of IMA rate.
Both VEGF164 and VEGF164b were more abundantly expressed in the chorion than in the amnion consistent with previous findings (Cheung et al. 1995). Since chorion levels did not change with experimental conditions and were not related to IMA rate, it appears that chorion VEGF may not be participating in modulating amniotic fluid transport. In this study, we did not detect a decrease in sFlt‐1 mRNA levels in the amnion when IMA rate was elevated, suggesting that sFlt‐1 was not interacting with VEGF to modify intramembranous transport as anticipated. This was consistent with the lack of relationship between sFlt‐1 and IMA rate.
Previous investigators have shown that application of VEGF to retinal endothelial cells increased permeability by mediating caveolar transport (Feng et al. 1999). We postulated that VEGF would similarly mobilize caveolae in amnion epithelial cells by up‐regulating caveolin‐1. However, in this study, caveolin‐1 mRNA level in the amnion was negatively correlated with VEGF164 mRNA. This finding does not support the notion that induction of VEGF would activate caveolin‐1 to enhance caveolar transcytosis.
We explored the effects of modifications in IMA rate on two known factors of VEGF activation: HIF‐1α (Forsythe et al. 1996) and PBEF (Astern et al. 2013). Our results did not detect significant changes in PBEF mRNA levels as IMA rate varied by more than an order of magnitude. On the other hand, HIF‐1α mRNA levels increased during elevated IMA rates in the absence of hypoxia. However, the lack of correlation between amnion HIF‐1α or PBEF mRNA levels with VEGF164 levels imply that these factors were minimally involved in regulating the expression of VEGF under each of the four experimental conditions.
Conclusions
Overall our findings provided new understanding of the transport components that are involved in the regulation of vesicular fluid movement across the amnion. First, the lack of change in caveolin‐1, flotillin‐1, or dynamin‐2 does not support the notion that alterations in the number of transport vesicles or the rate of their release from the plasma membrane was the underlying cause of the changes in IMA rate induced experimentally. Second, VEGF levels were not correlated with IMA rate, suggesting additional regulatory factors participate in the modulation of trans‐amnion vesicular transport. Third, the lack of a positive relationship between VEGF and its activators HIF‐1α and PBEF or a negative correlation with the antagonists VEGF164b and sFlt‐1 suggests that these VEGF agonists and antagonists would not be the unidentified stimulator(s) and inhibitor(s) of IMA found in the amniotic fluid. Fourth, the expression levels of caveolin‐1 and flotillin‐1 were significantly higher in the amnion than chorion, suggesting that transport vesicles may be more abundant in the amnion than chorion. Finally, an important finding in this study was the significant positive relationship between amnion tubulin‐α and IMA rate, and the down‐regulation of tubulin‐α when IMA rate was reduced. These responses were unique to the amnion and not detected in the chorion consistent with the concept that amnion is the rate‐limiting layer for amniotic fluid transport. Therefore, we conclude that intramembranous transport rate across the amnion may be regulated by the number, integrity and/or activity of intracellular microtubules.
Conflict Of Interest
There are no conflicts of interest for any of the authors. There is no information for disclosure.
Acknowledgments
The technical assistance of M. Beardall for the RT‐qPCR analysis is greatly appreciated.
Cheung C. Y., Anderson D. F., Brace R. A.. Transport‐associated pathway responses in ovine fetal membranes to changes in amniotic fluid dynamics. Physiol Rep, 5 (20), 2017, e13455, https://doi.org/10.14814/phy2.13455
Funding Information
This research was funded in part by grant R01 HD061541, National Institute of Child Health and Human Development, National Institutes of Health.
References
- Adams, E. A. , Choi H. M., Cheung C. Y., and Brace R. A.. 2005. Comparison of amniotic and intramembranous unidirectional permeabilities in late gestation sheep. Am. J. Obstet. Gynecol. 193:247–255. [DOI] [PubMed] [Google Scholar]
- Anderson, D. F. , Jonker S. S., Louey S., Cheung C. Y., and Brace R. A.. 2013. Regulation of intramembranous absorption and amniotic fluid volume by constituents in fetal sheep urine. Am. J. Physiol. Regul. Integr. Comp. Physiol. 305:R506–R511. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Astern, J. M. , Collier A. C., and Kendal‐Wright C. E.. 2013. Pre‐B Cell Colony Enhancing Factor (PBEF/NAMPT/Visfatin) and Vascular Endothelial Growth Factor (VEGF) cooperate to increase the permeability of the human placental amnion. Placenta 34:42–49. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bitsikas, V. , Correa I. R. Jr, and Nichols B. J.. 2014. Clathrin‐independent pathways do not contribute significantly to endocytic flux. Elife. https://doi.org/10.7554/eLife. 03970, September. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brace, R. A. 1977. Fitting straight lines to experimental data. Am. J. Physiol. 233:R94–R99. [DOI] [PubMed] [Google Scholar]
- Brace, R. A. , and Cheung C. Y.. 2011. Amniotic fluid volume and composition following fetal membrane resection in late gestation sheep. J Am Assoc Lab Animal Sci 50:939–942. [PMC free article] [PubMed] [Google Scholar]
- Brace, R. A. , and Cheung C. Y.. 2014. Regulation of Amniotic Fluid Volume: evolving Concepts. Adv. Exp. Med. Biol. 814:49–68. [DOI] [PubMed] [Google Scholar]
- Brace, R. A. , Gilbert W. M., and Thornburg K. L.. 1992. Vascularization of the ovine amnion and chorion: a morphometric characterization of the surface area of the intramembranous pathway. Am. J. Obstet. Gynecol. 167:1747–1755. [DOI] [PubMed] [Google Scholar]
- Brace, R. A. , Vermin W., and Huijssoon E.. 2004. Regulation of amniotic fluid volume: intramembranous volume and solute fluxes in late gestation fetal sheep. Am. J. Obstet. Gynecol. 191:837–846. [DOI] [PubMed] [Google Scholar]
- Brace, R. A. , Anderson D. F., and Cheung C. Y.. 2014a. Regulation of amniotic fluid volume: mathematical model based on intramembranous transport mechanisms. Am. J. Physiol. Regul. Integr. Comp. Physiol. 307:R1260–R1273. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brace, R. A. , Cheung C. Y., and Anderson D. F.. 2014b. Inhibitor of intramembranous absorption in ovine amniotic fluid. Am. J. Physiol. Regul. Integr. Comp. Physiol. 306:R185–R189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen, J. , Braet F., Brodsky S., Weinstein T., Romanov V., Noiri E., et al. 2002. VEGF‐induced mobilization of caveolae and increase in permeability of endothelial cells. Am. J. Physiol. Cell Physiol. 282:C1053–C1063. [DOI] [PubMed] [Google Scholar]
- Cheung, C. Y. 2004. Vascular endothelial growth factor activation of intramembranous absorption: a critical pathway for amniotic fluid volume regulation. J. Soc. Gynecol. Investig. 1:63–74. [DOI] [PubMed] [Google Scholar]
- Cheung, C. Y. , and Brace R. A.. 2008. Hypoxia modulation of caveolin‐1 and vascular endothelial growth factor in ovine fetal membranes. Reprod Sci 15:469–476. [DOI] [PubMed] [Google Scholar]
- Cheung, C. Y. , Singh M., Ebaugh M. J., and Brace R. A.. 1995. Vascular endothelial growth factor gene expression in ovine placenta and fetal membranes. Am. J. Obstet. Gynecol. 173:753–759. [DOI] [PubMed] [Google Scholar]
- Cheung, C. Y. , Li S., Chen D., and Brace R. A.. 2010. Regulation of caveolin‐1 expression and phosphorylation by VEGF in ovine amnion cells. Reprod Sci 17:1112–1119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cheung, C. Y. , Beardall M. K., Anderson D. F., and Brace R. A.. 2014. Prostaglandin E2 Regulation of Amnion Cell Vascular Endothelial Growth Factor Expression: relationship with Intramembranous Absorption Rate in Fetal Sheep. Am. J. Physiol. Regul. Integr. Comp. Physiol. 307:R354–R360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cheung, C. Y. , Anderson D. F., and Brace R. A.. 2016. Aquaporins in ovine amnion: responses to altered amniotic fluid volumes and intramembranous absorption rates. Physiol Rep 4:e12868 https://doi.org/10.14814/phy2.12868, July, 2016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Feng, Y. , Venema V. J., Venema R. C., Tsai N., Behzadian M. A., and Caldwell R. B.. 1999. VEGF‐induced permeability increase is mediated by caveolae. Invest. Ophthalmol. Vis. Sci. 40:157–167. [PubMed] [Google Scholar]
- Forsythe, J. A. , Jiang B. H., Iyer N. V., Agani F., Leung S. W., Koos R. D., et al. 1996. Activation of vascular endothelial growth factor gene transcription by hypoxia‐inducible factor 1. Mol. Cell. Biol. 16:4604–4613. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Galbiati, F. , Volonte D., Engelman J. A., Watanabe G., R. Burk , Pestell R. G., et al. 1998. Targeted downregulation of caveolin‐1 is sufficient to drive cell transformation and hyperactivate the p42/44 MAP kinase cascade. EMBO J. 17:6633–6648. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gesteland, K. M. , Anderson D. F., Davis L. E., Robertson P., Faber J. J., and Brace R. A.. 2009. Intramembranous solute and water fluxes during high intramembranous absorption rates in fetal sheep with and without lung liquid diversion. Am. J. Obstet. Gynecol. 201e1‐6. https://doi.org/10.1016/j.ajog.2009.02.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gilbert, W. M. , and Brace R. A.. 1989. The missing link in amniotic fluid volume regulation: intramembranous absorption. Obstet. Gynecol. 74:748–754. [PubMed] [Google Scholar]
- Gilbert, W. M. , Eby‐Wilkens E., and Tarantal A. F.. 1997. The missing link in rhesus monkey amniotic fluid volume regulation: intramembranous absorption. Obstet. Gynecol. 89:462–465. [DOI] [PubMed] [Google Scholar]
- Gross, S. , Devraj K., Feng Y., Macas J., Liebner S., and T. Wieland . 2017. Nucleoside diphosphate kinase B regulates angiogenic responses in the endothelium via caveolae formation and c‐Src‐mediated caveolin‐1 phosphorylation. J. Cereb. Blood Flow Metab. 37:2471–2484. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harvey, T. W. , Engel J. E., and Chade A. R.. 2016. Vascular endothelial growth factor and podocyte protection in chronic hypoxia: effects of Endothelin‐A Receptor Antagonism. Am. J. Nephrol. 43:74–84. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Head, B. P. , Patel H. H., and Insel P. A.. 1838. Interaction of membrane/lipid rafts with the cytoskeleton: impact on signaling and function: membrane/lipid rafts, mediators of cytoskeletal arrangement and cell signaling. Biochim. Biophys. Acta 532–545:2014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heald, R. , and Nogales E.. 2002. Microtubule dynamics. J. Cell Sci. 115:3–4. [DOI] [PubMed] [Google Scholar]
- Henley, J. R. , Krueger E. W., Oswald B. J., and McNiven M. A.. 1998. Dynamin‐mediated internalization of caveolae. J. Cell Biol. 141:85–99. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kendall, R. L. , and Thomas K. A.. 1993. Inhibition of vascular endothelial cell growth factor activity by an endogenously encoded soluble receptor. Proc. Natl Acad. Sci. 90:10705–10709. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Khan, S. , and Donnelly J.. 2017. Outcome of pregnancy in women diagnosed with idiopathic polyhydramnios. Aust. N. Z. J. Obstet. Gynaecol. 57:57–62. [DOI] [PubMed] [Google Scholar]
- King, B. F. 1993. Development and structure of the placenta and fetal membranes of nonhuman primates. J. Exp. Zool. 266:528–540. [DOI] [PubMed] [Google Scholar]
- Kirchhausen, T. , Owen D., and Harrison S. C.. 2014. Molecular structure, function, and dynamics of clathrin‐mediated membrane traffic. Cold Spring Harb Perspect Biol 6(5):a016725. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Li, H. H. , Li J., Wasserloos K. J., Wallace C., Sullivan M. G., Bauer P. M., et al. 2013. Caveolae‐dependent and ‐independent uptake of albumin in cultured rodent pulmonary endothelial cells. PLoS ONE 8(11):e81903 https://doi.org/10.1371/journal.pone, 0081903, November. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Liu, S. , Premont R. T., Singh S., and Rockey D. C.. 2017. Caveolin 1 and G‐protein‐coupled receptor kinase‐2 coregulate endothelial nitric oxide synthase activity in sinusoidal endothelial cells. Am. J. Pathol. 187:896–907. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Locatelli, A. , Vergani P., Toso L., Verderio M., Pezzullo J. C., and Ghidini A.. 2004. Perinatal outcome associated with oligohydramnios in uncomplicated term pregnancies. Arch. Gynecol. Obstet. 269:130–133. [DOI] [PubMed] [Google Scholar]
- Morris, R. K. , Meller C. H., Tamblyn J., Malin G. M., Riley R. D., Kilby M. D., et al. 2014. Association and prediction of amniotic fluid measurements for adverse pregnancy outcome: systematic review and meta‐analysis. BJOG 121:686–699. [DOI] [PubMed] [Google Scholar]
- Ngo, D. T. , Farb M. G., Kikuchi R., Karki S., Tiwari S., Bigornia S. J., et al. 2014. Antiangiogenic actions of vascular endothelial growth factor‐A165b, an inhibitory isoform of vascular endothelial growth factor‐A, in human obesity. Circulation 130:1072–1080. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nowak, D. G. , Woolard J., Amin E. M., Konopatskaya O., Saleem M. A., Churchill A. J., et al. 2008. Expression of pro‐ and anti‐angiogenic isoforms of VEGF is differentially regulated by splicing and growth factors. J. Cell Sci. 121:3487–3495. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robertson, P. , Faber J. J., Brace R. A., Louey S., Hohimer A. R., Davis L. E., et al. 2009. Responses of amniotic fluid volume and its four major flows to lung liquid diversion and amniotic infusion in the ovine fetus. Reprod Sci 16:88–93. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Salzer, U. , and Prohaska R.. 2001. Stomatin, flotillin‐1, and flotillin‐2 are major integral proteins of erythrocyte lipid rafts. Blood 97:1141–1143. [DOI] [PubMed] [Google Scholar]
- Schmittgen, T. D. , and Livak K. J.. 2008. Analyzing real‐time PCR data by the comparative C(T) method. Nat. Protoc. 3:1101–1108. [DOI] [PubMed] [Google Scholar]
- Shandley, L. , Alcorn D., and Wintour E. M.. 1997. Ovine amniotic and allantoic epithelia across gestation. Anat. Rec. 248:542–553. [DOI] [PubMed] [Google Scholar]
- Sharshiner, R. , Brace R. A., and Cheung C. Y.. 2017. Vesicular uptake of macromolecules by human placental amniotic epithelial cells. Placenta. 57:137–143. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shen, Z. Y. , Xu L. Y., Li E. M., Zhuang B. R., Lu X. F., J. Shen , et al. 2008. Autophagy and endocytosis in the amnion. J Structural Biol 162:197–204. [DOI] [PubMed] [Google Scholar]
- Shrem, G. , Nagawkar S. S., Hallak M., and Walfisch A.. 2016. Isolated oligohydramnios at term as an indication for labor induction: a systematic review and meta‐analysis. Fetal Diagn. Ther. 40:161–173. [DOI] [PubMed] [Google Scholar]