Abstract
Background
Anemia is a hematologic disorder with decreased number of erythrocytes. Erythropoiesis, the process by which red blood cells differentiate, are conserved in humans, mice and zebrafish. The only known agents available to treat pathological anemia are erythropoietin and its biologic derivatives. However, erythropoietin therapy elicits unwanted side-effects, high cost and intravenous or subcutaneous injection, warranting the development of a more cost effective and non-peptide alternative. Ginger (Zingiber officinale) has been widely used in traditional medicine; however, to date there is no scientific research documenting the potential of ginger to stimulate hematopoiesis.
Methodology/Principal Findings
Here, we utilized gata1:dsRed transgenic zebrafish embryos to investigate the effect of ginger extract on hematopoiesis in vivo and we identified its bioactive component, 10-gingerol. We confirmed that ginger and 10-gingerol promote the expression of gata1 in erythroid cells and increase the expression of hematopoietic progenitor markers cmyb and scl. We also demonstrated that ginger and 10-gingerol can promote the hematopoietic recovery from acute hemolytic anemia in zebrafish, by quantifying the number of circulating erythroid cells in the dorsal aorta using video microscopy. We found that ginger and 10-gingerol treatment during gastrulation results in an increase of bmp2b and bmp7a expression, and their downstream effectors, gata2 and eve1. At later stages ginger and 10-gingerol can induce bmp2b/7a, cmyb, scl and lmo2 expression in the caudal hematopoietic tissue area. We further confirmed that Bmp/Smad pathway mediates this hematopoiesis promoting effect of ginger by using the Bmp-activated Bmp type I receptor kinase inhibitors dorsomorphin, LND193189 and DMH1.
Conclusions/Significance
Our study provides a strong foundation to further evaluate the molecular mechanism of ginger and its bioactive components during hematopoiesis and to investigate their effects in adults. Our results will provide the basis for future research into the effect of ginger during mammalian hematopoiesis to develop novel erythropoiesis promoting agents.
Introduction
The bone morphogenetic protein (Bmp) signaling pathway plays a critical role in hematopoeisis during the induction and maintenance of Hematopoietic Stem Cells (HSCs) in the “Aorta-Gonad-Mesonephros” (AGM) axis [1]–[2]. Bmp’s are members of the TGF-β superfamily of secreted factors, which regulate the development of multiple organ systems, such as bone, neural and renal tissue. In addition to their function in dorsal-ventral specification, Bmp’s regulate the development of human HSCs [3] and embryonic hematopoiesis (blood cell formation) during early vertebrate development, but this function is independent of their mesoderm inductive activity [4]. In zebrafish, bmp2b, bmp4 and bmp7a expression is especially important for ventral mesoderm patterning [5]–[7] and blood specification [8]–[9]. Bmp signaling is required to initiate the HSC program at the floor of the dorsal aorta and to maintain normal levels of HSC descendants during hematopoeisis [10]–[11]. In mammals, the blood cells originate in the blood islands of the yolk before they are produced in the body of the embryo [12]. In adults, the bone marrow is the primary tissue for hematopoeisis and erythropoiesis, with blood cells originating from stem cells; however, the molecular nature of this process is not well understood [13]. Similarly, in the vertebrate zebrafish, blood cells form in different sites during early embryonic development starting from the mesoderm near the aorta (ICM or Intermediate Cell Mass) and then at the posterior blood island (PBI) in the tail. These sites are of special interest because they contain hematopoietic progenitors which give rise to the blood cells and can be used as a model to study the molecular mechanism of hematopoeisis and erythropoiesis in vivo [12]–[13].
The AGM, arising from the mesodermal primary cell layer, is the main site for hematopoeisis in mammals [14], and the addition of Bmp to long term cultures of AGM-derived HSCs increases their growth and survival [15]. The zebrafish equivalents of these tissues, arising also from the mesoderm, are the ICM and the PBI, where the hematopoietic progenitor markers cmyb, scl and lmo2 are expressed during development [16]–[22]. In both mammals and zebrafish, hematopoeisis occurs in two distinct steps, the ‘primitive’ and ‘definitive’ waves. The ICM and PBI represent the site of ‘primitive’ or first wave of hematopoeisis. The ICM contains hemangioblasts, which can differentiate into pro-erythroblasts or angioblasts (blood/vessel precursors), whereas the PBI generates erythro-myeloid precursors, including pro-erythroblasts and myeloblasts [16]. The zinc finger transcription factor GATA-binding protein 1 (gata1) is a master regulator of erythrocyte commitment and maintenance [23]. gata1 and spleen focus forming virus proviral integration oncogene (spi1/pu1) determine the erythroid vs. myeloid cell fates respectively to maintain balance of both cell lineages [24]. In mice, the subsequent ‘definitive’ wave of hematopoiesis gives rise to hematopoietic stem cells (HSCs) capable of differentiating into any of the blood cell lineages; hematopoiesis takes place in both the aorta-gonad-mesonephros (AGM) region and the umbilical vessels at embryonic stage E10–11 [14], [25]. As development progresses, erythropoiesis gradually shifts from the spleen and liver of the fetus to the bone marrow in mammals [13], equivalent to the kidney marrow in zebrafish. Real-time observations in live reporter transgenic animals have confirmed that the transition from hemogenic endothelium in the ventral wall of the aorta to HSCs actually occurs in the mouse, zebrafish and Xenopus [18]–[19], [25]–[26]. In zebrafish, the definitive wave of hematopoiesis occurs in the kidney marrow and thymus after a transient development in the PBI-derived caudal hematopoietic tissue (CHT) and the hemogenic endothelium in the ventral wall of the dorsal aorta [17], [27]. Stage-specific transcription during definitive hematopoiesis is driven by runt-related transcription factor 1 (runx1) and avian myeloblastosis viral oncogene homolog (cmyb) [28].
The erythropoiesis-stimulating agents available to treat pathological anemia, commonly associated with end stage renal disease and cancer chemotherapy, such as Aranesp, Procrit, Epogen and Neorecormon, are biologic derivatives or various formulations derived from the same protein, erythropoietin (EPO). However, the side effect of using EPO therapy includes life-threatening cardiovascular complications. Another drawback of using EPO and its analogs is the high cost and the injectable mode of delivery, therefore warranting the development of a non-peptide alternative. Here, we identified a natural product, namely ginger (Zingiber officinale), which can stimulate hematopoiesis in zebrafish embryos. By using a chemically inducible hemolytic anemia model, we showed that ginger extract and its active component 10-gingerol (10-G) can promote hematopoietic recovery in a process that is mediated via the bmp signaling pathway.
Results
Ginger (Zingiber officinale) and its Bioactive Components
Ginger is widely used as both a spice and an herbal medicine for rheumatism, nausea, colds and flu, diarrhea, muscular disorders, dyspepsia, poor appetite and diabetes [29]. Gingerols, the major phenolic components of ginger [30] and shogaols, the dehydrated forms of gingerols, possess anti-inflammatory and anti-cancer properties [29], [31]–[32]. In the present study, we purified various gingerols and shogaols using previously published methods with slight modifications [31] and confirmed their structures by 1H and 13C NMR analysis (Figure S1). Ginger extract and the purified 6-, 8-, 10-gingerol (6-G, 8-G, 10-G) and 6-, 8-, 10-shogaol (6-S, 8-S, 10-S) were used in the following experiments to evaluate their potential to promote hematopoiesis in the zebrafish model.
Ginger Promotes Gata1 Expression
The GATA-binding factor 1 (Gata1), a zinc finger transcription factor, is an early marker and key regulator of erythropoiesis. Erythrocytes can be visualized in vivo in Tg(gata1:dsRed) transgenic zebrafish embryos by fluorescence microscopy as they exhibit an erythrocyte-specific red fluorescence under the control of the gata1 promoter [33]. Here, we studied the hematopoeisis promoting effect of ginger extract and its components 6-, 8-, and 10-gingerol and 6-, 8-, and 10-shogaol in zebrafish embryos from the late gastrulation stage at 9 hour-post-fertilization (hpf) to the 21 hpf stage before the onset of circulation. Figure 1 illustrates that treatment with ginger extract or its components, including 8-G, 10-G, 8-S and 10-S, resulted in increased fluorescence intensity of Tg(gata1:dsRed) transgenic expression at 1 day-post-fertilization (dpf) (Figure 1A), both in the ICM and the PBI. In addition, whole-mount in situ hybridization analyses using a specific gata1 anti-sense RNA probe confirmed that exposure of Tg(gata1:dsRed) zebrafish embryos to ginger extract (5–10 µg/ml) and 10-G (as low as 2 µg/ml) promoted gata1 expression in developing erythrocytes (Figure 1B). At 2 dpf, when the heart has begun to beat rhythmically and blood circulation is established, we observed an increase in gata1:dsRed fluorescence signal in circulating erythroid cells within the vasculature, especially in zebrafish treated with 5 µg/ml ginger and 2 µg/ml 10-G (Figure 1C). These results suggest that ginger extract (5–10 µg/ml) and its components 8-G, 10-G, 8-S and 10-S (2–5 µg/ml) potentially stimulate hematopoiesis. Our data identified 10-G as the most potent bioactive component of ginger extract in promoting the primitive wave of erythropoiesis and the least toxic to early developing zebrafish embryos. In Figure 2A, pictures of double transgenic Tg(flk1:GFP);Tg(gata1:dsRed) embryos show the expansion of the PBI caudal region, where a cavity has emerged surrounded by a hypertrophic vascular plexus and filled with Tg(gata1:dsRed) erythrocyte progenitor cells at 22 hpf, following exposure to ginger extract (5 µg/ml) or 10-G (5 µg/ml). After the establishment of circulation, the morphology of the PBI of these treated embryos is indistinguishable from their untreated siblings, although they have much more circulating erythrocytes (Figure 1C). These data provide evidence that ginger and its bioactive components could potentially stimulate erythropoiesis during the primitive wave of hematopoiesis in early developing zebrafish embryos.
To further delineate the effect of ginger in promoting erythrocyte differentiation, we analyzed the effect of ginger on a mouse erythroblast cell line (ATCC-TIB55/BB88) in vitro. Figure S2 shows that the mouse erythroblasts remained undifferentiated in the control conditions of 0–0.05% DMSO. On the other hand, ginger treatment (5–20 µg/ml) significantly promoted erythrocyte differentiation of mouse erythroblasts as we detected the production of hemoglobin using benzidine staining [34]. A similar level of cell viability was obtained in all treatments after 5 days (70–80% viable cells; unpublished data), using trypan blue staining. High concentration of ginger (20 µg/ml) for 5 days induced differentiation of erythrocytes (3.3%) in contrast to 0% in control. At the same time, the treatment with ginger led to a reduction in the number of proliferating cells as compared to the control (24.3%; Figure S2). The effect of ginger is dose dependent, as we observed fewer (0.93%) differentiated erythrocytes, and a significant increase in the number of proliferating cells (13.3%; Figure S2) at lower concentration of ginger (5 µg/ml). Overall, the effect of ginger on erythrocyte differentiation in vitro is not significant enough to account for the increase in the number of erythroid cells induced by ginger in vivo. For this reason, we further investigated the effect of ginger on hematopoietic progenitor cells in vivo.
Ginger Promotes Expression of Hematopoietic Progenitor Markers
Like all vertebrate organisms, zebrafish show waves of hematopoiesis during development [12]. Zebrafish hematopoiesis originates from the cmyb-positive primitive hematopoietic progenitors arising in the ventral mesoderm-derived ICM/PBI [23]. In 48 hpf embryos, cells expressing cmyb are scattered among the first progenitors of definitive hematopoiesis along the ventral wall of the dorsal aorta; in zebrafish, this thin mesenchyme between the dorsal aorta and the posterior cardinal vein corresponds to the mammalian AGM [5]–[6], [27]. At 4 dpf, cmyb is weakly expressed in the trunk and tail in hematopoietic clusters, but by 5 dpf, it is mainly expressed in the caudal vein plexus (CHT), pronephric glomeruli and thymi.
The CHT reaches its maximal activity by 5–6 dpf, although it remains hematopoietic until at least 14 dpf, associated with the definitive wave in the caudal vein plexus and supporting proliferation and differentiation of blood precursors. To analyze the effect of ginger on hematopoietic progenitors, we used whole-mount in situ hybridization to detect the expression of cmyb transcription factor (a marker of immature hematopoietic cells whose expression decreases as these cells differentiate) and stem cell leukemia hematopoietic transcription factor, also named T-cell acute lymphocytic leukemia 1 (scl/tal1, a marker for hemangioblasts, already fated to become hematopoietic cells). Figure 2 shows that exposing late gastrulation (9 hpf) embryos to ginger (5 µg/ml) or its bioactive component 10-G (2 µg/ml) up-regulates the expression levels of hematopoietic progenitor markers, such as cmyb (Figure 2B) and scl/tal1 (Figure 2C), in the ICM/PBI region at 22 hpf. These data suggest that ginger or 10-G treatments could increase primitive erythropoiesis in zebrafish embryos through the promotion of the hematopoietic progenitor cell numbers.
Mechanistic Insight: Ginger Induces bmp7a/2b Expression
When zebrafish embryos were treated during early development with high concentrations of ginger, i.e. 15 to 20 µg/ml from the shield stage (6 hpf) to 1 dpf, we observed a severe defect with mercedes mutant-like tail phenotype, characterized by a partial duplication of the tail fin [35]–[36] (Figure 3A) and ventralization of embryos, exhibiting a swollen yolk sac extension with excessive Tg(gata1:dsRed) fluorescent erythrocytes accumulating in the ICM/PBI before the onset of blood circulation. Most importantly, these observed phenotypes are reminiscent of an enhanced Bmp activity during early development.
To determine whether ginger modulates bmp/smad signaling, we used whole-mount in situ hybridization to analyze temporal-spatial gene expression of bmp2b, bmp4 and bmp7a, following ginger or 10-G treatment of zebrafish embryos. As shown in Figure 3B, early short-term (3-hour) exposure of zebrafish embryos during gastrulation to ginger extract (5 µg/ml) and 10-G (1 µg/ml) from the sphere stage (4 hpf) to 60% epiboly stage (7 hpf), increased the level and extended the domain of bmp7a expression. At this stage bmp7a expression is normally restricted to the ventral side of the blastoderm, but ginger and 10-G treatments induced expression throughout the entire blastoderm. In addition, ginger exposure during gastrulation (but not 10-G) results in a small delay in the progression of embryonic cell epiboly, whereas the epibolic movement of the yolk syncytial layer is not affected (Figure 3B–D).
As shown in Figure 3C, early treatment of embryos (from the sphere stage) with ginger or 10-G also resulted in an increase in the expression of bmp2b and expanded its expression domain towards the dorsal side at 60% epiboly stage, but did not induce the intense global expression seen with bmp7a. We observed no change in bmp4 expression in response to ginger or 10-G exposure (Figure S3).
To further delineate the bmp signal axis, we determined the expression of bmp target genes even-skipped-like1 (eve1, a ventral mesodermal marker) [35] and GATA-binding protein 2 (gata2, a non-neural ectodermal marker) [37] and observed an increase in their mRNA levels, following early exposure to ginger (5 µg/ml) or 10-G (1 µg/ml) from sphere (4 hpf) to 60% epiboly (7 hpf) stages (Figure 3D–E). Hence, we provide evidence that treatment of early embryos with ginger extract or 10-G, one of its individual active components, increases the expression of bmp2b/7a and two bmp target genes, eve1 and gata2.
The bmp signaling pathway is regulated by the action of dorsalizing signals from extracellular protein factors coded by genes such as chordin (chd) [38], and fibroblast growth factor8 (fgf8) and bmp signaling pathways interact during ventral mesoderm patterning in blood formation [39]; therefore, we analyzed the expression of chd and fgf8 in early stage embryos. No change in their transcript levels was seen following exposure to ginger extract from 3 hpf to shield (6 hpf) stages (Figure S4). Our results are consistent with a previous study by Miller-Bertoglio and colleagues who had shown that chd expression is indistinguishable in weakly ventralized mercedes mutant embryos at 75% epiboly and their wildtype siblings [38]. Thus, the hematopoietic effect of ginger is independent of the mRNA expression of chd at the dorsal organizer and fgf8 at the dorsal and ventral margins from 3 hpf to shield stages (Figure S4).
Ginger Induces bmp7a/2b Expression in the CHT Region
In order to separate the hematopoietic and mesoderm inductive effects of ginger/10-G on the bmp signaling during early embryonic development, we investigated the bmp2b/7a expression profiles following exposure to ginger/10-G, from 10 hpf to 48 hpf (Figure 4). In untreated control embryos, bmp2b is weakly expressed in the ventral fin epidermis, the ventral posterior mesoderm (hematopoietic), the caudal vein and the posterior cardinal vein during the primitive wave of hematopoiesis. The exposure of embryos to ginger/10-G, starting after the completion of gastrulation, triggers an up-regulation of bmp2b expression only in these ventral posterior tissues of the future CHT at 32 hpf (not shown). The contrast in bmp2b expression patterns between control embryos and ginger/10-G-treated embryos is even more outstanding at 48 hpf, when the bmp2b expression in the ventral posterior mesoderm has become down-regulated in the untreated control embryos, which show no expression in the CHT area, unlike the ginger/10-G treated embryos which exhibit an over expression of bmp2b restricted to the CHT region and the corresponding portion of the caudal ventral fin (Figure 4A). We also analyzed the expression patterns of bmp7a at 48 hpf after ginger or 10-G exposure and observed its up-regulation in the same region including the CHT and the underlying fin (Figure 4B). Thus, during the transition from the primitive to the definitive wave of hematopoiesis, exposure of zebrafish embryos to ginger extract (5 µg/ml) or 10-G (2 µg/ml) locally up-regulates the expression of bmp2b and bmp7a in the area of the developing hematopoietic tissue.
Bmp Inhibitors Block Ginger-induced bmp Expression
We next screened bioactive small molecules known to inhibit Bmp/Smad signaling, such as dorsomorphin, LDN193189 and DMH1, to investigate if the ginger-mediated increase in bmp2b/7a transcription in the CHT region can be repressed by these specific signaling inhibitors through the Bmp auto-regulatory loop. Figure S5-A shows bmp2b expression at 48 hpf after treatment from 10 hpf with ginger alone versus combinations of ginger and inhibitors of Bmp/smad signaling, following ranges of concentrations in accordance with their documented specificities in the literature. For instance, Yu and colleagues used 10 µM dorsomorphin to induce a spectrum of dorsalization phenotypes in zebrafish embryos, which vary with the developmental stage of treatment, by specifically antagonizing receptors ALK2/3/6 and not AMPK or VEGFR2 signaling. They also show that dorsomorphin preferentially inhibits BMP/Smad over MAPK p38, TGF-β and Activin signaling [40]. We tested a range of concentrations for combining dorsomorphin (0.1–10 µM) with ginger, and determined that 0.1 µM was sufficient to inhibit the local over-expression of bmp2b in the CHT area mediated by ginger (Figure S5). We also tested the dorsomorphin analogues LDN-193189 and DMH-1 using a narrower range of concentrations (0.1–1 µM), as both molecules were shown to be more selective and more potent in blocking Bmp/Smad signaling, without interfering with VEGF or TGF-β signaling [41]–[42]. As shown in Figure S5, 0.1 µM DMH-1 highly antagonized the ginger-induced bmp2b over-expression in the CHT region. In this assay, the Bmp type I receptor antagonists DMH-1 and dorsomorphin were slightly more potent than the LDN-193189 analogue in blocking the effect of ginger (Figure S5, bottom table). We observed similar results by analyzing bmp7a expression profiles in 48 hpf embryos in the same Bmp type I receptor antagonist screening assay (Figure S6). Altogether, these results suggest that ginger and 10-G can induce bmp expression specifically in the ventral tail area including the developing caudal hematopoietic tissue.
Ginger Enhances Hematopoietic Recovery from Anemia
To further demonstrate that ginger and 10-G stimulate hematopoiesis in a quantitative manner, we established a protocol to measure the number of erythrocytes circulating in the caudal artery (Videos S1 and S2) during hematopoietic recovery (Figure 5A and D) using a phenylhydrazine-inducible hemolytic anemia zebrafish model [6]. Transgenic Tg(gata1:dsRed) zebrafish embryos were exposed to 0.5 µg/ml phenylhydrazine from 33 hpf to 48 hpf and then washed extensively (Videos S3 and S5). The anemic embryos were subsequently treated with ginger extract (Video S4) or 10-G (Video S6) starting at 54 hpf. Videos of erythrocytes circulating within the caudal artery, in a portion of the dorsal aorta in the tail region beyond the proctodeum, were acquired at 5 and 6 dpf using a fluorescent microscope (see Methods for detail). For each video, we counted the number of Tg(gata1:dsRed) cells entering and exiting the filmed portion of the dorsal aorta. The average was calculated and subsequently corrected by the blood flow ratio. Video analyses indicated that exposure to ginger extract (2 µg/ml) (Figure 5B) produced a 2.4-fold increase in the number of circulating Tg(gata1:dsRed) cells compared to phenylhydrazine controls at 5 dpf. When the embryos were treated with the ginger component 10-G (1 µg/ml), we observed a 2.3-fold increase in circulating blood cells (Figure 5C) compared to phenylhydrazine controls at 6 dpf. Therefore, exposure to ginger or 10-G promotes recovery from phenylhydrazine-induced acute hemolytic anemia in zebrafish by increasing the number of circulating Tg(gata1:dsRed) erythroid cells. As compared to normal control zebrafish embryos (Video S7), phenylhydrazine treatment completely eliminated circulating Tg(gata1:dsRed) cells at 3 dpf (Video S8); therefore, erythrocytes produced/recovered from phenylhydrazine treatment after 3 dpf were most likely derived from erythroid progenitors (erythroblasts) generated by definitive hematopoietic tissues.
Bmp Signaling is Essential for Ginger-induced Hematopoietic Recovery
Since bmp expression is up-regulated in response to ginger or 10-G exposure in zebrafish embryos, we asked whether Bmp signaling was essential for ginger-induced hematopoietic recovery by inhibiting its downstream target Bmp-activated Bmp type I receptor kinase. Inhibition of this receptor kinase, using the specific pharmacological antagonist dorsomorphin [40], will block Bmp-mediated Smad phosphorylation. The inhibition of Bmp signaling during gastrulation is not feasible since Bmp signals are crucial to early development [38]; therefore, we treated embryos with dorsomorphin in combination with ginger or 10-G at 54 hpf beyond the time when Bmp activity is essential for dorsal-ventral patterning. The effect of ginger or 10-G on hematopoiesis is completely abolished by a low concentration (0.1 µM) of dorsomorphin in phenylhydrazine-induced anemic zebrafish (Figure 6A and B; Videos S9 and S10). The treatment of control embryos and anemic embryos with dorsomorphin alone has no significant effect on the number of circulating Tg(gata1:dsRed) cells (Figure S7). We repeated these analyses using the dorsomorphin analogue DMH-1 (0.1 µM), which exclusively targets the Bmp but not Vegf signaling [42]. We observed the same suppression of ginger-induced erythroid recovery at 5 dpf (Figure S8). Altogether, these quantitative data show that ginger extract or 10-G can boost the hematopoietic recovery from anemia via a Bmp/Smad signaling-dependent mechanism.
As a result, we investigated the hematopoietic progenitors during the second or definitive wave of hematopoiesis at 6 dpf by whole-mount in situ hybridization using the hematopoietic progenitor markers cmyb, scl and lmo2. When the zebrafish embryos were treated with ginger or 10-G during the period from 54 hpf to 6 dpf, they exhibited stronger expression of cmyb along the CHT and the hemogenic endothelium (Figure 7A–C; cartoon Figure 6C) in comparison with control embryos. The same increase in cmyb expression in the CHT and the hemogenic endothelium was observed in anemic embryos treated with ginger or 10-G (Figure 7D–F). In addition, ginger exposure also up-regulates the expression of scl/tal1 and lmo2 transcription factors in the CHT, especially in anemic zebrafish embryos (Figure S9). scl is expressed in progenitors during development and serves as an early marker of hemangioblasts that are already fated to become hematopoietic cells. Lmo2 (LIM domain only 2, also known as Rhombotin-like 1) is required for hematopoietic stem cell differentiation, similar to Scl, which interacts with Lmo2 in a multiple transcription factor complex required for the specification of early blood cells and the regulation of the early hematopoietic program in the developing embryo. Hence, our data suggests that ginger or 10-G treatments not only increase the primitive wave of hematopoiesis (Figures 1 and 2), but also enhance the number of hematopoietic progenitors during the definitive wave (Figures 7 and S9).
Altogether, our data are consistent with previous observations in mammals showing that Bmp is necessary for the proliferation of HSCs [1]. The exposure of normal and phenylhydrazine-treated embryos to ginger extract or its active phenolic component, 10-G, at 54 hpf induced the expression of bmp2b and bmp7a restricted to the CHT region at 3 dpf (Figures 8 and 9 respectively), whereas bmp expression is already down-regulated in control embryos at this stage. This ginger-induced up-regulation of bmp2b/7a localized in the CHT area is likely to lead to the activation of the Bmp/Smad signaling and the over-expression of hematopoietic progenitor markers such as cmyb (Figure 7), scl/tal1 and lmo2 (Figure S9). Eventually, it increases the number of circulating Tg(gata1:dsRed) erythroid cells, which is normally regulated by the Bmp pathway, especially during recovery from chemically-induced anemia (Figures 6 and S8).
Discussion
Overall, our results demonstrate that ginger extract and its purified component 10-G potentially stimulate both the primitive and definitive waves of hematopoiesis in zebrafish embryos. We also show that the treatment with ginger or 10-G promotes the hematopoietic recovery from phenylhydrazine-induced anemia in this model. Finally, we provide mechanistic evidence that the hematopoiesis-promoting effects of ginger and 10-G are mediated through the modulation of bmp expression and Bmp signaling pathway in zebrafish (Figures 4, 8, 9, S5, S6, 6, S7 and S8).
In the literature, bmp2b expression patterns have not been documented after 38 hpf by in situ hybridization [43] and bmp7a expression data are available until 24 hpf only [44]. In the present study, we show expression of bmp2b/7a at 8 hpf and 48 hpf in control embryos and in embryos exposed to ginger/10-G, where we observed an up-regulation of their transcription in the CHT region at 48 hpf (Figure 4). We also illustrated expression of bmp2b/7a at 79 hpf in normal and anemic embryos and showed that upon ginger/10-G exposure from 54 hpf, the same ectopic induction of their expression in the area of the CHT can be observed (Figures 8 and 9). Indeed, Wiley et al. have shown that bmp2b is expressed in the caudal vein plexus at 32 hpf, but not at 26 hpf or 38 hpf [43], in accordance with our observations in control embryos at 32 hpf (not shown) and 48 hpf (Figures 4, S5, S6).
In zebrafish and other vertebrates, Bmp signal plays an essential role during gastrulation and regulates dorsal-ventral patterning in concert with Nodals, Wnts and Fgfs: high ratio of BMP signaling promotes ventral fates including blood, vasculature and pro-nephritic ducts. In adult fish, kidney marrow is the site of hematopoiesis, Smad-mediated Bmp signaling was also detected in the proximal and distal kidney in bmp response element transgenic zebrafish line [45]. The same study also illustrated the normal expression of phosphorylated Smad1/5/8 in 3 dpf larvae at the tip of the tail, as well as ventrally anterior to the proctodeum, thus including the transient hematopoietic tissues during definitive hematopoiesis.
In Mammals, it is now clear that the BMP signaling pathway plays a critical role in the maintenance of HSC potential in the Aorta-Gonad-Mesonephros (AGM) region [11]. Another study confirmed that BMP increases the growth and survival of AGM HSCs in long-term culture [15]. Yet one group showed that BMP7, but not BMP2 or BMP4, improves maintenance of human primitive peripheral blood-derived hematopoietic progenitor cells [2]. Our findings that ginger extract induces bmp expression in the area of the transient caudal hematopoietic tissue, cmyb in hematopoietic progenitors and gata1 in erythrocytes and erythroid progenitors of zebrafish embryos are consistent with another study, as Bmp is well known for its bone promoting ability, where mouse fetuses exposed to ginger extract were heavier and had more advanced skeletal development than control embryos [46]. Therefore, future studies to explore the outcomes of various combinations of ginger components on hematopoiesis in mammalian models may provide new insights for nutraceutical development to promote erythropoiesis for treating pathological anemia.
Materials and Methods
Zebrafish Husbandry
Zebrafish AB transgenic strains Tg(gata1:dsRed) [47] and Tg(flk1:GFP) [48] have been described previously; embryos were staged and maintained according to NCCU IACUC guidelines. Zebrafish embryos with or without ginger or gingerol components were incubated at 28.5°C in 0.3X Danieau’s solution (19.3 mM NaCl, 0.23 mM KCl, 0.13 mM MgSO4, 0.2 mM Ca(NO3)2, 1.7 mM HEPES, pH 7.0) containing 30 µg/ml phenylthiourea (PTU, added after late gastrulation stages) to inhibit pigmentation. Following or prior to exposure to ginger or phenolic compounds, embryos were washed, dechorionated and anaesthetized before observations, picture acquisitions, or fixation in 4% paraformaldehyde (PFA).
Whole-mount in situ Hybridization
The in situ hybridization procedure has been described previously [49] as probes: cmyb [18], gata1 [33], gata2 [35], eve1 [35], scl [21], lmo2 [22], bmp2b [50], bmp4 [51], bmp7a [51].
Fluorescent Microscopy
Imaging was performed using an Olympus MVX10 MacroView Fluorescence Microscope (Olympus, Center Valley, PA) with Hamamatsu C9300-221 high-speed digital CCD camera (Hamamatsu City, Japan). For time-lapse imaging, transgenic Tg(gata1:dsRed) fluorescent embryos were anaesthetized in tricaine and imaged at 5 or 6 dpf. Picture acquisition parameters were kept constant to allow direct comparisons. Raw data were analyzed using MetaMorph TL for Olympus software (Olympus, Center Valley, PA) and exported in QuickTime format.
Quantitation of Erythrocytes
The effect of ginger and 10-G on hematopoiesis was quantified after induction of acute hemolytic anemia using 0.5 µg/ml phenylhydrazine (PHZ). PHZ was added into the incubation medium (0.3X Danieau’s solution) of 33 hpf Tg(gata1:dsRed) positive embryos, followed by extensive washes at 48 hpf. Embryos were then incubated with ginger or 10-G and/or dorsomorphin (DMP; 0.1 µM). Videos of circulating erythrocytes within the caudal artery were taken at 5 or 6 dpf under a fluorescence microscope. The videos of circulating erythrocytes were analyzed in a minimum of 25 embryos per experimental condition by counting the number of Tg(gata1:dsRed) fluorescent cells entering/exiting the artery section (100 frames in 2.5 seconds; 327 µm distance). Average calculated numbers of erythrocytes were normalized with blood flow (velocity) ratio. In order to perform this normalization, three independent cells were chosen arbitrarily to count the number of frames required for each cell to cross the filmed portion of the dorsal aorta (327 µm x 246 µm). The average number of frames was then used to calculate the flow rate and to normalize the number of Tg(gata1:dsRed) cells in the assay condition with the PHZ control using the flow rate ratio (PHZ control flow rate/assay flow rate). This analysis was performed for 25–30 embryos per experimental condition, the average was calculated for all parameters and Student’s t-tests were used to determine statistical significances. Data presented for fluorescent erythrocyte counts in Tg(gata1:dsRed) transgenic embryos are mean ± SEM. To analyze the difference between two groups, p values were determined by using the Student’s t-test. p<0.01 was considered statistically significant. The quantitation procedure was repeated in 3 independent experiments for ginger and for 10-G using DMP to inhibit Bmp/Smad signaling. It was also repeated in 2 independent experiments using the DMP analogue DMH-1 (0.1 µM).
Isolation of the Major Gingerols and Shogaols from Ginger Extract
6-, 8-, and 10-gingerol and 6-, 8-, and 10-shogaol were purified from ginger extract in our laboratory using previously reported methods with slight modifications [31]. In brief, the ginger extract was chromatographed on a Diaion HP-20 column eluted first with 50% aqueous ethanol to obtain fraction A, followed by 75% aqueous ethanol to obtain fractions B and C, and finally 95% aqueous ethanol to obtain fraction D. Following our previous methods, 6-gingerol was purified from fraction A, 6-shogaol and 8- and 10-gingerol were purified from fraction B, and 8- and 10-shogaol were purified from fraction C. The purification procedure was guided by thin layer chromatography (TLC) and high-performance liquid chromatography (HPLC) analysis. The structures of these six compounds were confirmed by 1H and 13C NMR analysis [31].
Incubation with Ginger and its Components
Ginger extract, 6-, 8-, 10-gingerol and 6-, 8-, 10-shogaols were dissolved in dimethyl sulfoxide (DMSO) to prepare the stock solutions. Ginger extract and its purified compounds were diluted in 0.3X Danieau’s solution containing PTU. The final concentration of DMSO in experiments was less than or equal to 0.05% (v/v; 0.002 to 0.05%), which has no effect on differentiation nor proliferation of BB88/TIB-55 cells or zebrafish embryonic development.
Cell Culture
The murine erythroleukemia (BB88/TIB-55) cell line [52]–[53] (ATCC, Rockville, MD) was cultured in ATCC-formulated RPMI-1640 supplemented with 50 µM 2-mercaptoethanol, 10% ATCC FBS and antibiotics. Cells were cultured at 37°C in a humidified atmosphere of air with 5% CO2. BB88 cells (erythroblasts) were induced to differentiate into erythrocytes by transiently adding 1.8% dimethyl sulfoxide (DMSO; positive control) or ginger extract (5, 10 and 20 µg/ml; assays). 0.0125%, 0.025% and 0.05% DMSO were used as additional negative control for ginger extract.
Benzidine Staining of Hemoglobins
1 ml of benzidine stock solution (2 g/L benzidine dihydrochloride in double-distilled water containing 2.9% (v/v) glacial acetic acid) was mixed with 20 µl of 33% H2O2 to prepare the working solution. Cells were mixed with the benzidine working solution at a 1∶1 (v/v) ratio, incubated 2–3 minutes, and hemoglobin positive cells were scored using a hemocytometer (blue cells). Trypan blue exclusion viability analyses were performed in parallel.
Supporting Information
Acknowledgments
We thank Dr. Leonard Zon at Boston Children’s Hospital for the Tg(gata1:dsRed) transgenic zebrafish; Dr. Suk-Won Jin at Yale Medical School for the Tg(flk1:GFP) transgenic zebrafish; Dr. David Traver at University of California at San Diego for in situ probes (cmyb); Dr. Matthias Hammerschmidt at the University of Cologne, Germany for probes (bmp2b, bmp4, bmp7a); Cheyenne McKibbin, Jody Duprey, Jamil Heider and Pooja Pardhanani for technical assistance; Drs. Susan Yeyeodu, Xiaohe Yang and Soniya Sinha for critical reading of the manuscript.
Footnotes
Competing Interests: The authors have declared that no competing interests exist.
Funding: This work was partially supported by the North Carolina Biotechnology Center (2009-BRG-1213 to TCL) and the National Institutes of Health (CA138277 and CA138277S1 to SS). No additional external funding received for this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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