EFFECTS OF SOLUTE SIZE AND TISSUE COMPOSITION ON MOLECULAR AND MACROMOLECULAR DIFFUSIVITY IN HUMAN KNEE CARTILAGE

Abstract

Objective:

Articular cartilage is an avascular tissue. Accordingly, diffusivity represents a fundamental transport mechanism for nutrients and other molecular signals regulating its cell metabolism and maintenance of the extracellular matrix. Understanding how solutes spread into articular cartilage is crucial to elucidating its pathologies, and to designing treatments for repair and restoration of its extracellular matrix. As in other connective tissues, diffusivity in articular cartilage may vary depending both its composition and the specific diffusing solute. Hence, this study investigated the roles of solute size and tissue composition on molecular diffusion in knee articular cartilage.

Design:

FRAP tests were conducted to measure diffusivity of five molecular probes, with size ranging from ~332Da to 70,000Da, in human knee articular cartilage. The measured diffusion coefficients were related to molecular size, as well as water and glycosaminoglycan (GAG) content of femoral and tibial condyle cartilage.

Results:

Diffusivity was affected by molecular size, with the magnitude of the diffusion coefficients decreasing as the Stokes radius of the probe increased. The values of diffusion coefficients in tibial and femoral samples were not significantly different from one another, despite the fact that tibial samples exhibited significantly higher water content and lower GAG content of the femoral specimens. Water content did not affect diffusivity. In contrast, diffusivities of large molecules were sensitive to GAG content.

Conclusions:

This study provides new knowledge on the mechanisms of diffusion in articular cartilage. Our findings can be leveraged to further investigate osteoarthritis and to design treatments for cartilage restoration or replacement.

INTRODUCTION

Osteoarthritis (OA) is the most prevalent joint disorder in the United States, affecting 1 in 2 adults and costing upwards of $100 billion annually in the US alone [1]. Moreover, the majority of OA cases occur in the articular cartilage in the knee, making it the most susceptible joint. Available treatments of OA are limited, and generally include symptoms management and joint arthroplasty in the late stages [2]. Recently, intra-articular delivery of agents, such as drugs or cytokines, has been heralded as a promising new strategy for the treatment of knee OA [3, 4]. In order to design novel strategies for the efficient transport and delivery of drugs into the tissue, understanding the mechanism of molecular transport in cartilage is necessary.

Transport mechanisms in articular cartilage are affected by the tissue structure and composition [5]. Cartilage is a highly hydrated tissue, with water making up approximately 70% of the wet weight of the tissue. The extracellular matrix (ECM) is primarily composed of collagen type II and aggrecans [6, 7]. The ECM of articular cartilage is negatively charged due to the presence of aggrecans, which contain negatively charged glycosaminoglycan (GAG) side chains. This negative fixed charge density contributes to the swelling property of the tissue, which is key to its mechanical functioning in the joint. Overall, the densely packed arrangement of the ECM significantly hinders solute transport in the tissue, especially for larger and branched molecules [8–10]. The average pore size of the tissue is approximately 6 nm, which is similar in size to some of the proposed therapeutic agents [5]. However, additional molecule properties, such as shape and charge, also play critical roles in their delivery and transport in cartilage.

Articular cartilage is also an avascular tissue, which means that essential molecules, including nutrients, metabolic wastes, and other molecules such as cytokines, growth factors, and enzymes, must be transported through the ECM from the surrounding vasculature. This transport may occur by diffusion or by convection (i.e., fluid flow due to tissue compression). In general, the transport of small solutes, such as nutrients, is primarily via diffusion, whereas that of larger molecules may be augmented by fluid flow [11–18]. In order to more fully understand the nutritional supply and pathophysiology of articular cartilage, knowledge of transport mechanisms through the tissue is essential. The diffusion of a wide range of molecules has been measured in articular cartilage from human and animal sources, see reviews [5, 19, 20]. These studies have shown that solute size and mass strongly influence molecular transport in articular cartilage, with an inverse relationship between solute size and diffusion coefficient which holds for a wide range of molecular sizes.

In order to better understand tissue pathophysiology, an expanded knowledge of transport mechanisms in cartilage is crucial. To successfully translate the potential of intra-articular drug delivery for the clinical treatment of OA, the rate and efficiency of delivery of different molecules must be known. Similarly, such information is needed for developing novel tissue engineered replacement tissues, which will need to interface with native tissue and allow for efficient transport of molecules. Quantitative data and structure-function relations for molecular transport in cartilage can also be employed in computational modeling of cartilage, which can be utilized for designing new therapies. Thus, the results of this study have the potential to contribute to the development of novel strategies to treat and/or repair articular cartilage in a variety of areas. Earlier studies have investigated the diffusivity of a range of solutes in knee cartilage, the majority of which was measured in animal tissues [20]. Here, we investigate solute diffusion in human articular cartilage, which will allow for a more direct clinical translation of these results to develop new regenerative approaches to treating OA.

In this study, we investigated the diffusivity of a range of solutes in articular cartilage harvested from the femoral condyles and the tibial plateaus of human knees. Solutes ranged in size from 332 Da to 70,000 Da, which captures sizes ranging from nutrients, growth factors, and potential drugs for the treatment of OA. Using our custom fluorescence recovery after photobleaching (FRAP) technique[21–23], we measured the diffusion coefficient of 6 differently sized molecules using a consistent experimental design, which allows for direct comparison within our results for different solutes in human cartilage. In order to understand the influence of the tissue ECM composition on solute transport, we sought to correlate the diffusion coefficient with the tissue water and GAG contents, two critical compositional features of cartilage. This study provides a comprehensive picture of solute diffusion in human articular cartilage, which will contribute to new knowledge on transport behavior in the tissue that can be translated to new therapeutic strategies to treat OA.

MATERIALS AND METHODS

Molecular probes:

A broad range of sizes of the molecular probes was selected to provide an inclusive picture on diffusivity of solutes as small as nutrients (~200Da) to those as large as growth factors, enzymes, cytokines and potential drugs for treatment of osteoarthritis (from few hundreds of Da to hundreds of thousands of Da). Accordingly, the following probes were selected: fluorescein, insulin, bovine serum albumin (BSA), and two dextrans (D3K and D70K), see Table 1 for details.

Table 1.

Summary of molecular probes used in this study.

Molecule	Source	Abbreviation	MW [Da]	rs (Å)	Concentration in PBS [M]
Fluorescein	Sigma-Aldrich	Fluorescein	332	5.02a	10−4
Insulin-FITC labeled human	Sigma-Aldrich	Insulin	5,807	10.5b	4.3 × 10−5
Albumin from Bovine Serum (BSA), Alexa Fluor™ 488 conjugate	Molecular Probes	BSA	66,000	34.8c	3.8 × 10−6
Dextran, Fluorescein, 3000 MW	Molecular Probes	D3K	3,000	14d	1.7 × 10−4
Dextran, Fluorescein, 70000 MW	Molecular Probes	D70K	70,000	60d	1.8 × 10−5

^a[49];

^b[50];

^c[51];

^d[52]

Specimen preparation:

Tissue samples were harvested after autopsy from eight femurs and eight tibias of age ranging from 60 to 72 y.o. Before tissue harvesting, knees were visually inspected to determine the degradation grade of the articular cartilage, which was deemed to be 0 or 1 according to Outerbridge classification [24]. Subsequently, using a Small Joint OATS system (Arthrex, Inc. Naples, FL) cylindrical cartilaginous plugs of 5mm diameter were obtained from femoral and tibial medial condyles. Each plug was placed in a compresstome (VF-210–0Z, Precisionary Instruments, Inc., Natick, MA) to obtain a cylindrical sample of 0.5mm height from the upper radial zone of the cartilage [25]. Similar to our previous studies [22, 26], specimens were confined within two porous plates and a perforated impermeable spacer, and equilibrated overnight in a PBS solution (Sigma-Aldrich Co., St. Louis, MO) containing the molecular probe of interest. Molar concentrations for each solute investigated are reported in Table 1. For each molecule investigated, 8 tibial samples and 8 femoral samples were tested (one sample from each tibia and one from each femur), and a minimum of 3 FRAP tests were performed and averaged on each sample. For each condyle investigated, additional tissue samples, for measurements of water and GAG content, were obtained from the cartilage region adjacent to that where specimens for diffusivity measurements were harvested. A schematic of specimen harvesting and preparation is reported in Figure 1.

Figure 1:

Schematic of specimen preparation. Location and size of the specimens is shown. For FRAP tests, cylindrical specimens with a height of 0.5 mm and a diameter of 5 mm were prepared from the central region of the meniscus along the axial direction. Additional specimens were harvested for measurement of water and GAG content in the tissue.

Measurement of diffusivity:

A custom FRAP technique was used to yield solutes diffusion coefficients (D) in the tissues [22]. Briefly, it was assumed that diffusive fluorescence recovery was a two-dimensional (2D) phenomenon occurring in the focal plane (x,y) of the microscope objective, following Fick’s second law. It was also assumed that the concentration of fluorescent probe was proportional to the intensity of its fluorescent emission. Hence, the mass balances over the diffusing fluorescent probe reads:

$$\frac{\partial c}{\partial t}=\nabla \cdot \left(D\nabla c\right),$$ (1)

where c denotes the molar concentration of the probe and D is the diffusion coefficient. Equation (1) can be transformed and solved in the 2D Fourier space defined by the dimensionless frequencies (u,v) [27]:

$$\frac{C\left(u,v,t\right)}{C\left(u,v,0\right)}=\text{exp}\left[-4{\pi }^2\left(u^2+v^2\right)Dt\right],$$ (2)

where C(u,v,t) is the 2D Fourier transform of c(x,y,t). The values of D can be determined by curve-fitting of experimental data, represented by confocal microscope video images, with Equation (2).

Experiments were carried out at room temperature (22 °C) using a confocal laser scanning microscope (A1R-SI, Nikon, Japan). The specimens were excited and photobleached by an argon laser (488 nm wavelength) using a Plan Apo 20x/0.75 DIC N2 WD 1.0 objective (Nikon, Japan), and emitted fluorescence in the green range of wavelengths. To minimize the error due to the out-of-plane diffusivity contribution, a multi-layer bleaching protocol was implemented as previously reported [21, 22, 26]. Each test consisted of five pre-bleach images followed by a time series of 200 post-bleach images. The size of the images was 128×128 pixel (460.7×460.7 μm²), with an initial circular bleach spot of 16 pixel diameter. The time lapse between two consecutive images was 0.25s. In order to minimize the contribution of the fluorescence emission of the background, pre-bleach images were averaged and then subtracted from the post-bleach image series. Image analysis was carried out using a custom MATLAB-based algorithm [23].

Measurement of tissue composition: Determination of Tissue Composition:

The contents of water, and GAGs in the cartilaginous specimens was measured. Specifically, specimens were weighed immediately after preparation (W_wet) and after lyophilization (W_dry). Weight measurements were conducted using an analytical balance (Model ML104, Mettler Toledo, Columbus, OH) with a readability of 0.1 mg and a repeatability of 0.1 mg. Average values of W_wet and W_dry were 22 mg and 5 mg, respectively. The fraction of water content was measured as:

$${\phi }^w=\frac{W_{\mathit{\text{wet}}}-W_{\mathit{\text{dry}}}}{W_{\mathit{\text{wet}}}}.$$ (3)

Subsequently, following an established experimental protocol [28], a DMMB assay was utilized to determine the masses of GAGs, whose mass fraction was defined with respect to tissue dry weight as:

$${\phi }^{\mathit{\text{GAG}}}=\frac{W_{\mathit{\text{GAG}}}}{W_{\mathit{\text{dry}}}}.$$ (4)

Statistical Analysis:

A first question of interest was to determine the effect of solute size on the magnitude of diffusivity in both tibia and femur cartilage. Accordingly, ANOVA followed by post-hoc Tukey test was used to investigate significant differences in the magnitudes of diffusion coefficients across solutes. Also, two-sample t-test was used to determine whether, for each solute investigated, the type of tissue (femoral or tibial cartilage) had any significant effect on the magnitude of the diffusion coefficient. Moreover, a simple linear regression model was used to investigate correlation among solute diffusion coefficients and their Stokes radii (r^s). Additional simple linear regression models were used to investigate correlations among solutes diffusion coefficients and water and GAG content in the cartilage samples. All the statistical analyses were conducted using Minitab®19 statistical software (Minitab, LLC, State College, PA). For each test conducted, a level of significance of 0.05 (α = 0.05) was used. All the data are reported in terms of mean ± standard deviation.

RESULTS

A summary of the measured diffusion coefficients for all the molecular probes and tissue type investigated in this study is reported in Table 2. In both femoral and tibial cartilage, the magnitudes of diffusivities were significantly different between molecular probes (p < 0.01) with those of fluorescein being the largest (114.1±32.6 μm²/s and 107.8.5±26.1, respectively), and those of D70K being the smallest (14.7±0.9 μm²/s and 14.3±1.2 μm²/s, respectively). Also, for each molecular probe investigated, the magnitudes of D in femoral and tibial cartilage were not statistically different (p > 0.05). Therefore, in all the subsequent statistical analyses and data representations, values of diffusion coefficients in femoral and tibial cartilaginous samples were pooled together. Through a simple linear regression analysis, it was found that D was positively correlated to the inverse of the Stokes radii (R² = 0.91), see Figure 2.

Table 2.

Summary of molecular probes diffusivities. Data are reported in terms of mean ± standard deviation. Grouping of pairwise comparison obtained after Tukey test are reported.

Molecular Probe	Femur		Tibia
	D [μm2/s]	Grouping	D [μm2/s]	Grouping
Fluorescein	114.1±32.6	A	107.8.5±26.1	A
Insulin	60.4±15.1	B	62.2±12.9	B
D3K	69.2±11.6	B	66.5±15.2	B
BSA	39.3±6.4	C	38.3±6.0	C
D70K	14.7±0.9	D	14.3±1.2	D

Figure 2:

Diffusivity is related to the inverse of the solute Stokes radius. For the data reported in the figure, diffusion coefficients of tibial and femoral cartilage were averaged together.

A summary of tissue composition measurements is reported in Table 3. A significant difference (p < 0.05) in tissue composition between tibial and femoral samples was observed: tibial samples were characterized by larger water content (0.75±0.02) and less GAG content (0.078±0.004) when compared to femoral samples (0.71±0.02 and 0.087±0.006, respectively).

Table 3.

Summary of tissues composition. Data are reported in terms of mean ± standard deviation.

Tissue	Water fraction on total weight (ϕw)	GAG fraction on dry weight
Tibia	0.75±0.02	0.078±0.004
Femur	0.71±0.02	0.087±0.006

In investigating the effect of tissue water content on solute diffusivity, only the values of D associated to fluorescein, D3K and BSA exhibited a significant (p < 0.05), yet weak (R² < 0.2) positive correlation with φ^w, Figure 3.

Figure 3:

Relationship between solute diffusivity and water content: (a) Fluorescein; (b) D3K; (c) Insulin; (d) D70K; (e) BSA. For each solute investigated, diffusion coefficients of tibial and femoral cartilage samples were pooled together.

Stronger relationships were found among GAG content and diffusivities: the values of D for D3K and D70K were positively correlated to φ^GAG (R² = 0.67 and R² = 0.22, respectively), while those for BSA were negatively correlated to the amount of GAGs in the tissue (R² = 0.46). Diffusivities of fluorescein and insulin were not significantly affected by GAG content (p > 0.05), see Figure 4.

Figure 4:

Relationship between solute diffusivity and GAG content: (a) Fluorescein; (b) D3K; (c) Insulin; (d) D70K; (e) BSA. For each solute investigated, diffusion coefficients of tibial and femoral cartilage samples were pooled together.

DISCUSSION

This study investigated the solute diffusive transport of a wide range of molecular probes and their relationship with molecular size and tissue composition in the articular cartilage of the human knee.

Experiments were conducted on condyle cartilage form the tibia and femur. Measurements of tissue composition indicated that femoral samples were characterized by a larger GAG content and a lower water content when compared to the tibial ones, see Table 3. However, despite the difference in composition, diffusivities in tibial and femoral samples were not statistically different from one another, for any of the solutes investigated in the study. Instead, as reported in previous studies (see review [19]), diffusivity was inversely related to solutes’ molecular weight, see Table 2. Specifically, fluorescein (~332Da) was associated with the largest measured diffusion coefficient ~110μm²/s. There are no records of measurements of fluorescein diffusivity in articular cartilage. However, the values reported in this study seem reasonable when considering that sucrose (~342Da) diffusivity in human cartilage was estimated to be ~130μm²/s [29], and similar values of diffusivity have been reported for other cartilaginous tissues, such as intervertebral disc, meniscus and temporomandibular joint [21, 22, 26, 30, 31]. The diffusion coefficients associated with D3K and insulin were not statistically different from each other, and ranged between ~60 and ~70μm²/s. Such a range of values is in agreement with previous measurements of D3K diffusivity in animal tissue, ranging from 30 to 76μm²/s [32, 33], and insulin diffusion coefficient in human and bovine tissue, varying from 22 to 93μm²/s [29, 34, 35]. Also, the diffusion coefficient of BSA was measured to be ~38μm²/s, which is comparable to the range of 20 to 38μm²/s associated to spherical molecules of similar size [36]. Finally, the smallest diffusion coefficient was that of D70K, measuring ~14μm²/s. This value was about half of that measured in human and animal tissue [33, 35, 37], but not largely different from what measured in superficial porcine cartilage (<20μm²/s) [33].

Several models describing the mechanisms of solute diffusivity in porous media have been proposed, and relate solutes diffusion coefficients to their hydrodynamic radii and characteristic structural dimensions of the media, among other parameters [38–40]. Cartilage is a porous medium and it would be reasonable to expect that its diffusive properties could be described by one of the proposed models in the literature. However, DiDomenico and Bonassar showed that existing theoretical models relating diffusivity in cartilage to the size of the diffusing probe are suboptimal. In their study, the authors propose an empirical power law relationship to predict the magnitude of diffusion coefficients of spherical probes as a function of their hydrodynamic radius [19]. This study investigated both spherical (fluorescein, insulin and BSA) and linear (D3K and D70K) molecular probes. The measured diffusion coefficients were found to be inversely related to the Stokes radii of the molecular probes, following a relationship reminiscent of the Stokes-Einstein, see Figure 2. Similar findings were reported for dextran molecules diffusing in porcine knee cartilage [33]. However, it should be noted that the empirical relation reported in Figure 2 presents the limitation of having been determined by pooling together spherical and linear molecular probes, whose diffusion mechanisms in the cartilage may be different and, therefore, not directly comparable.

The effect of tissue composition of solute diffusivity was also investigated by attempting to establish empirical relations with water and GAG content in the tissue. The results indicated that water content had a negligible effect on solute diffusivity: correlations between φ^w and D were only significant for fluorescein, D3K and BSA, with R² values smaller than 0.2, see Figure 3. Change in water content in the tissue may alter the distance between collagen fibers constituting the solid mesh of the cartilage. Nevertheless, collagen has not been considered to be a significant influence on the diffusion of most molecules in cartilage because of the large spacing existing among fibers [11]. This may explain the minimal effect played by φ^w and D hereby reported. It should be also noted that measurements of water content were conducted on tissue samples adjacent to those used for FRAP. As such, small regional variations might have contributed to difficulty in direct correlation. Conversely, proteoglycans are believed to contribute to hindering solute diffusivity in cartilage [11, 35], and our results indicate that GAG content significantly affected the magnitude of the diffusion coefficients of D3K, D70K and BSA, see Figure 4. Specifically, for the case of BSA, diffusivity was inversely related to φ^GAG (Figure 4e), corroborating evidence on the hindrance role played by GAGs on molecular mobility. In contrast, the magnitudes of the diffusion coefficients of D3K and D70K were positively correlated to the GAG content (Figures 4b–d). Dextran macromolecules are linear and may follow diffusive mechanisms substantially different from those expressed by spherical solutes, such as BSA [19]. In fact, a direct proportionality between D70K and GAG content has been previously reported for the case of porcine cartilage [33]. Finally, the lack of significant correlation among φ^GAG and D of fluorescein and insulin may be attributed to the small size of these molecules, which makes their mobility less sensitive to structural organization of the tissue when compared to larger solutes.

Several limitations of this study should be noted. The results reported are based on human tissues obtained during autopsy, and only a limited range of tissue degenerative states and composition was obtained. To achieve more general results, in the future, the experimental cohort used in this study will need to be supplemented by additional data obtained from tissue samples including a broader range of biochemical composition. In any case, the fact that this study was based on human tissues provides clinical and translational relevance to the reported findings. Also, the investigation of this study was limited to electrically neutral molecular solutes. Charged solutes, by interacting with the negatively charged solid phase of the cartilaginous tissue, exhibit unique diffusive behavior [8, 36, 41–44]. Accordingly, future studies including charged solutes are planned in order to more fully understand solute transport behavior in the articular cartilage. Moreover, the study of the effect of tissue composition on molecular diffusivity was limited to the investigation of water and GAG components, and neglected the examination of the potential contribution of collagen content. However, the potential hindering effect of collagen on solute diffusivity is not expected to be significant due to the large spacing existing among fibers [11]. Furthermore, human articular cartilage is usually subdivided into five regions, including the superficial, the transitional, the upper radial, lower radial and calcified zone [25]. These regions exhibit variations in matrix biochemical composition, cell morphology, and cell–matrix structural organization as a function of depth [45–48]. Studies on porcine articular cartilage have shown that solute diffusivity of dextrans ranging from 3 kDa to 500 kDa significantly changes from surface to middle or deep zone [33]. In this study, cartilage samples were taken from the upper radial zone. Further studies are required to determine whether the structural and compositional characteristics of other cartilage zones determine measurable changes in the solutes’ diffusion coefficients. Finally, all the samples used in this study were harvested from knees that were visually inspected to determine the degradation grade of their articular cartilage, which was deemed to be 0 or 1 according to Outerbridge classification [24]. Nevertheless, the subgroup of samples used for fluorescein measurements exhibited water and GAG contents lower than that found in the rest of the specimens, see Figure 3a and Figure 4a. This may suggest that such samples were harvested from a cartilaginous region presenting some extent of tissue degeneration which was not detectable via visual inspection.

In summary, this study presents a characterization of diffusive transport of a wide range of molecular solutes in the cartilage of the human femur and tibia, and its relationship with tissue composition. It was found that diffusivity is inversely related to solutes molecular weight and hydrodynamic radii. Specifically, diffusion coefficients followed a relationship similar to Stokes-Einstein. Tissue water content did not significantly affect diffusivity. In contrast, significant correlations were found among diffusivities of large molecules and GAG content. These findings are crucial for better understanding of transport properties in cartilaginous tissues, as well as for the future development of numerical models to be used for describing tissue homeostasis and testing treatments for OA.