Research Article | Open Access
Vibudha Nanduri, Beheita Moein, Avinash Raj Thatipalli, Gopal Pande, Anasuya Ganguly, "Histochemical and Molecular Characterization of Spongiosal Cells in Native Tissue, Two- and Three-Dimensional Cultures of Rat Aortic Valve", Journal of Histology, vol. 2016, Article ID 7680701, 8 pages, 2016. https://doi.org/10.1155/2016/7680701
Histochemical and Molecular Characterization of Spongiosal Cells in Native Tissue, Two- and Three-Dimensional Cultures of Rat Aortic Valve
The histocytochemical and molecular analysis of cells that constitute the aortic valve (AV) of the rat heart was done in this study. We have focussed on the identity of cells in the spongiosal layer of the valve by immunofluorescence studies using lineage specific markers and cytochemical staining. We have established two-dimensional (2D) cultures of cells from isolated rat AV leaflets and maintained endothelial and interstitial valvular cells (IVC) over a period of six to eight weeks. Using “passage 0” cells from 2D valvular cultures, we could reconstruct the three-dimensional (3D) valvular tissue in collagen gels that showed very similar cellular organization and marker expression profile, as that of the native tissue. Lineage specific markers in the native tissue and cell cultures were studied by Reverse Transcriptase-PCR and immunofluorescence for VCAM-I, α-SMA, collagen I, CD71, collagen II, and E-cadherin markers. This is the first report on the identification of cell lineages in the spongiosal layer of AV and the successful reconstruction of 3D valvular tissue from primary cell cultures of AV.
Human and murine hearts comprise four valves (aortic, pulmonary, mitral, and tricuspid valve) that are located on a single valvular plate (Figure 1(a)(i)). Our interest was to study the cellular architecture of aortic valve (AV) in rat hearts which is located between the left and right atrioventricular annuli and connects the left ventricle and the ascending aorta . AV is one of the semilunar valves and it comprises three leaflets attached to a common annular ring; each leaflet is composed of three different layers, namely, the fibrosa (F), spongiosa (S), and ventricularis (V) (Figure 1(a)(iv)). The F layer is situated away from the blood flow and constituted by dense collagen fibres; V layer, located adjacent to the blood flow, is elastic in nature and it contains thin collagen fibres; S layer is situated between the F and V layer and it has high proteoglycan and elastin content that facilitates the valve to absorb high pressure and allow flexible movement. Each layer in the valve leaflet exhibits their specific functions due to the composition and organization of the cells in the extracellular matrix. Considering the F layer, it provides immense strength to the valve during blood flow. The S layer enhances the movement between the layers and acts as a shock absorber during closing of the valves. Due to the elastic nature of V layer, the extracellular matrix on the surface of the valve leaflet is stretched and retracted during the cardiac cycle. The mechanical properties of the three layers of leaflets provided by the collagen and elastin fibres help in proper function of heart during the cardiac cycle [2–5]. So far, the cellular composition of S layer has not been studied in detail and this layer is considered to have very few cells, the identity of which is not clear.
Due to various disorders and malfunctions associated with heart valves, ex vivo reconstruction of valves, using tissue engineering approaches, has been attempted in many labs [6–13]. However, as most of these methods have used nonbiological or acellular materials, the identity of cells in the reconstructed valves remains unclear.
Here, we have attempted to identify cells in the S layer of rat AV by studying lineage specific marker expression and doing cytochemical analysis of the primary tissue and cultured cells. The specific location and orientation of rat AV leaflets and isolation of primary tissue from the S layer have been illustrated in Figures 1(a) and 1(b). We have adopted tissue engineering methodologies for establishing 2D and 3D cultures of rat AV cells and characterized the cultured cell types by immunocytochemistry and molecular analysis. These 3D cultures allow the cells to grow with their neighboring conditions in all three dimensions. These cultures are mainly used for in vivo cells and models. 3D cultures help in cell-cell or cell-matrix interactions at higher rates, especially during the presence of a biological material, like that of collagen.
2. Materials and Methods
2.1. Collection of Wistar Rat Aortic Valve
All studies were performed on the hearts of healthy Wistar rats (8–12 weeks old) after fulfilling the requirements of Institutional Animal Ethics Committee (registration number: CPCSEA 20/1999). The area around the junction of the aorta with the right ventricle was dissected and the entire valvular plate containing the four heart valves was isolated. The AV was separated and cut open to expose the leaflets (see Figures 1(a)(i), 1(a)(iii), and 1(a)(iv)). Figure 1(a)(ii) describes the layout of the S layer in the leaflet. The valvular tissue was made free from all the surrounding muscle and the three valvular leaflets, with an average wet weight 0.2 g, were isolated and processed for further studies.
2.2. Tissue Fixation and Embedding
2.2.1. Histocytochemical Methods
The AV tissue (measuring about 0.25 cm2) is longitudinally opened, fixed in 10% buffered formalin for 7 days, processed sequentially in grades of 70%, 80%, 95%, and 100% isopropyl alcohol and chloroform (each step of processing with different grades of alcohol was done for 25 minutes), and finally embedded into wax blocks (Figure 1(b)). The procedure was followed as per the protocol described elsewhere . 4 μm thick serial sections of the tissue (Figure 1(b)) were cut using a Leica RM 2135 microtome and stained using Hematoxylin and Eosin (H and E), Toluidine Blue (TB) for total proteoglycan , and Masson’s trichrome (MT) for total collagen (procedure number HT15, Sigma-Aldrich, India).
2.2.2. Tissue Processing
Primary valvular cells from AV were prepared according to a standardized protocol described in literature elsewhere [15, 16]. Description of experiments and methodology of both 2D and 3D cultures are given below.
Two-Dimensional (2D) Cultures. Four normal AV leaflets, devoid of any extra muscular tissue and the aortic wall, were separated from the valvular plate and pooled. The pooled leaflets were minced in small volumes (200–300 μL) of DMEM (DMEM high glucose, Sigma-Aldrich, India) and the cell/tissue suspension was filtered through 100 μm sterile nylon mesh (BD Falcon, India). The tissue pieces that were left on top of the mesh were sequentially treated in enzymatic solutions, prepared in 1x PBS, and filter sterilized using 0.22 μm syringe filters in the following order: 0.2% trypsin (Cat. number T4049, Sigma-Aldrich, India) and 0.08% collagenase type IV (Cat. number C5138, Sigma-Aldrich, India), at 37°C for 30 minutes each. Cells obtained after enzymatic treatment were collected by centrifugation, counted and plated onto T25 culture flask (BD Falcon, India) at an average seeding density of 4 × 105 cells/cm2, and maintained in complete medium (CM) (DMEM comprising 1x glutamax and 1x penicillin-streptomycin (both from Gibco, India), 10% FBS (Sigma-Aldrich, India)) for a period of 20 days, with alternate day media changes. On reaching confluence, the cells were subcultured till passage 3 (P3) and maintained for 7 days in each passage. At each passage, cells were both cryopreserved, processed for immunocytochemical and molecular analysis and to establish 3D cultures.
Three-Dimensional Cultures (3D). Valvular cells from AV grown in 2D cultures for 20 days (P0) were suspended in collagen type I gels (Cat. number 3447-020-01, Invitrogen, India), prepared at 2 mg/mL in alkaline PBS at the concentration of 1.5 × 104 cells/mL; 100 μL of this suspension was added to Millicell 24-well culture inserts (Cat. number PIHT 12R 48, India) placed in a 24-well culture plate (BD Falcon, India), under aseptic conditions. Same volume of plain collagen gel devoid of valvular cells was used as a control. Both the gels were left undisturbed for 60 minutes at 37°C, after which the gel gets solidified. Once the gel gets firm, 200 μL of CM was added in each well, and the cultures were maintained for 30 days with media changes twice a week. After the 30-day period, the collagen gels with and without the valvular cells were processed for histology, immunofluorescence, and RT-PCR.
Various antibodies were used to study the different cell lineage patterns that were expressed in the native AV, 2D valvular cells, and 3D-reconstructed AV. Primary antibodies (all obtained from Abcam, USA) used for the study were as follows: rat anti-VCAM1 (ab78712), rabbit anti-α SMA (ab5694), rabbit anti-collagen I (ab34710), rabbit anti-collagen II (ab53047), rabbit anti-E cadherin antibody (ab53033), and mouse anti-CD71 (ab112215). All the secondary antibodies (obtained from Invitrogen, India), conjugated with Alexa Fluor 594 used for the study, included goat anti-rabbit IgG (A11012), goat anti-rat IgG (A11007), and goat anti-mouse IgG (A11032). The same immunofluorescence protocol was used for sections of native and 3D-reconstructed aortic valves. 4 μm thick sections were deparaffinised with xylene, treated with different ethanol concentrations in sequence, and placed in sodium citrate buffer (pH, 6.0) for heat-mediated antigen retrieval. For 2D cultures of valvular cells, the cells were first grown on 18 mm2 coverslips and then fixed with 4% paraformaldehyde and dried. For sections as well as the cells, blocking of nonspecific antibodies was done by treatment with 3% bovine serum albumin (BSA) in PBS. The sections and the cells were treated with 1 : 100 dilutions of their respective primary antibodies for 1 hour at room temperature and washed with PBS, and then 1 : 1000 dilutions of their relevant secondary antibodies were added and mounted with DAPI fluoroshield. Specific fluorescence for Alexa Fluor 594 goat anti-rabbit IgG antibody and DAPI was observed in a Zeiss Apotome fluorescence microscope comprising a 20x Plan-Apochromatic objective and filter settings of 594 nm/620 nm and 350 nm/470 nm as the excitation/emission wavelengths. Image analysis studies were done using AxioVision Rel 4.7 software (Zeiss).
2.2.4. Gene Expression Profiling
Total RNA was extracted from four pooled native AVs (1.2 mg/mL), valvular cells-2D cultures (0.78 mg/mL) and 3D-reconstructed AV tissue (1 mg/mL) using TRIzol reagent (Cat. number 1015, Bioserve, India). The extracted RNA was purified by DNAse (Cat. number 18068-015, Invitrogen) treatment, and 1 μg RNA of each sample was reverse transcribed using Super-Script III First-Strand Synthesis System for RT-PCR (Cat. number 18080-051, Invitrogen, India). The PCR was performed using the DNA Engine Peltier Thermal Cycler (Bio-Rad, India) for analysing the expression of high performance liquid chromatography- (HPLC-) purified nucleotide primers of rat GAPDH (the house-keeping gene) , collagen II , collagen I, αSMA , VCAM I , E-cadherin , and CD71  genes, obtained from Bioserve, India. Primer sequences for these genes are taken from the references mentioned above. To analyse GAPDH expression, the following PCR conditions were considered: hot start, 95°C, 2 minutes; 30 cycles of denaturation, 95°C, 30 seconds; annealing, 57.5°C, 30 seconds; and elongation, 72°C, 30 seconds. This was followed by final extension at 72°C, 5 minutes. The PCR conditions to study the expression of the remaining genes were similar to those used for GAPDH, but with the changes in the annealing temperatures of 58°C for collagen II, 65°C for collagen I and αSMA, 58°C for VCAM I, 55°C for E-cadherin, and 60°C for CD71. Safe View Classic (Cat. number G108, Applied Biological Materials, India) in 1% agarose gel was used to visualize the amplified products.
3.1. Native AV Histology
Figure 2 illustrates the H and E staining which was used to delineate the cellular organization of the three layers of AV. F layer showed low cell content, S layer had large nuclei and rich matrix, and the V layer exhibited higher cell number with each cell showing high cytoplasmic content. TB staining revealed a differential proteoglycan content in all the three layers of which S layer showed the highest expression. MT stained tissue highlighted the total collagen content in all the layers and once again the S layer showed the highest collagen specific staining.
3.2. Lineage Specific Marker Expression
Marker expression to identify specific cell lineages was studied by immunofluorescence as described. Figure 3 shows that VCAM-I (endothelial cells) and αSMA (interstitial valvular cells) were expressed in all three layers with maximum expression in the S layer; CD71 (mesenchymal cells) and collagen I (fibroblastic cells) were expressed at higher levels in the V layer; E-cadherin (epithelial cells) and collagen II (chondrocytic cells) were expressed at very low levels in all the three layers. These observations confirm that VCAM I and αSMA are the main markers expressed in the S layer indicating that this layer is composed mainly of IVC and endothelial cells.
3.3. Two-Dimensional Culture Studies
Primary cells isolated from AV leaflets as described were maintained in CM for a period of 20 days (P0) or 7 days (P1, P2, and P3 each). Figure 4 describes the phase contrast microscopy images of the cells maintained from P0 to P3. We can clearly observe that there is a gradual decrease in cell size from P0 to P3, and this could be due to the cellular and matrix differentiation that occur during the culture process.
To confirm cell lineages in the 2D cultures, immunofluorescence of VCAM I, αSMA, collagen I, collagen II, E-cadherin, and CD71 was performed. This analysis was done in 10 different experiments that showed similar results as shown in Figure 5. Though the cell size decreased gradually during P0–P3 (Figure 4), the expression of VCAM I and αSMA remained consistently high through the passages. Similar to the observations in primary AV tissue (Figure 3), expression of collagen I and CD71 showed moderate expression and expression of collagen II and E-cadherin was at very low levels. These data confirm that, in 2D cultures, maintenance of endothelial cells and IVC was more than other cell types.
3.4. Three-Dimensional Culture Studies
Primary AV leaflet cells first grown in 2D cultures were collected 3 weeks after plating and then transferred into collagen type I gels in 24-well millicell culture inserts as described in Section 2. Collagen gels, with and without AV cells, were stained with H and E, TB, and MT and the results are shown in Supplementary Figure A in Supplementary Material available online at http://dx.doi.org/10.1155/2016/7680701. Interestingly, H and E staining pattern of cells in the 3D culture showed a systematic arrangement of the F, S, and L layers. TB and MT staining of the gels also showed maximum expression of total proteoglycan and collagen contents in S layer. These staining patterns of 3D gels mimic the distribution cell in the native AV tissue.
Immunofluorescence for VCAM I, αSMA, collagen I, CD71, collagen II, and E-cadherin in 3D-reconstructed AV is shown in Supplementary Figure B. CM grown AV tissue clearly depicts the three layers, with higher expression of VCAM I and αSMA proving higher cellular content for endothelial and valvular interstitial cells, respectively. Collagen I and CD71 are expressed moderately all through the tissue, and collagen II and E-cadherin are expressed at very low levels.
3.5. Gene Profiling Analysis
A comparative study of native AV cells acquired from 2D and 3D AV culture systems was done by RT-PCR. Equal quantities of total RNA was used to study GAPDH (control), VCAM I, αSMA, collagen II, collagen I, CD71, and E-cadherin expression levels. Fifteen independent experiments were done and similar results that are depicted in Figure 6 were confirmed. High levels of expression of VCAM I and αSMA genetic markers were observed in native AV, 2D, and 3D cultures. Collagen II and E-cadherin remained consistently low in all of the three sources. Collagen I and CD71 showed moderate expression from the sources selected.
Our results confirm that among other cellular lineages, the endothelial and IVC origin cells were main representatives of the valvular tissue in 3D cultures and primary AV tissue.
Several earlier reports have described the histochemical architecture of heart valves especially the aortic valve [1, 23–25]. These studies have shown that all valves have a layered organization of which some layers face the direction of blood flow and some are away from it. The composition of the cells in these layers is related to the functions of the concerned layer [1–4, 23]. In the AV, three clear cut layers have been observed of which the ventricularis and the fibrosa that compose the external surfaces of the valve are better studied [2, 26]. The spongiosal layer which lies in the middle of the valve plays a crucial role in determining the flexibility and elasticity of the valve. As several diseases of AV affect its elastic and mechanical properties, therefore it is necessary to know the cellular and molecular composition of the S layer in better detail.
In this report, we have found that the S layer is primarily composed of endothelial and interstitial cells although their number is very low. As per the gross anatomy (Figure 2), the cells show a large nuclear organization and are deeply embedded within fenestrated structures that are distributed all through the S layer. Decrease in the cell number in 2D cultures is noticed which might be due to the rearrangement of cellular and matrix properties, the main feature of spongiosa layer. The cells express high levels of VCAM and αSMA and low or nil other markers. These properties of the spongiosal cells could also be reproduced in the 2D cultures at early passages and in the reconstructed tissues in the 3D cultures.
Based on these observations, we propose that future studies on the AV valve regeneration or reconstruction ex vivo can be achieved if correct combination of valvular endothelial cells and collagen matrix is combined in a 3D configuration.
Conflict of Interests
The authors declared no potential conflict of interests with respect to the authorship and publication of this paper.
Funding for this project was provided by Dr. Gopal Pande from the Council of Scientific and Industrial Research (Grant Code ESC 103) and by Dr. Anasuya Ganguly from Aditya Birla Science and Technology Group.
Supplementary Figure 1: (A) Histological studies of the 3D reconstructed AV tissue grown in CM, using collagen gel as a scaffold, at 20X magnification. (B) Immunofluorescence of the AV tissue grown in 3D cultures for 30 days in CM, at P0 and 40X magnification. DAPI (blue stain) stained nuclei; Alexafluor 594 nm (red stain) fluorescence for different markers as indicated. Scale bar is 100 μm.
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