Научная статья на тему 'ENDOTHELIAL DIFFERENTIATION OF WHARTON’S JELLY-DERIVED MESENCHYMAL STEM CELLS SEEDED ON CHITOSAN/HYALURONAN MULTILAYER FILMS'

ENDOTHELIAL DIFFERENTIATION OF WHARTON’S JELLY-DERIVED MESENCHYMAL STEM CELLS SEEDED ON CHITOSAN/HYALURONAN MULTILAYER FILMS Текст научной статьи по специальности «Биотехнологии в медицине»

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Cellular Therapy and Transplantation
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ВАК
Ключевые слова
MESENCHYMAL STEM CELLS / WHARTON’S JELLY / DIFFERENTIATION / ENDOTHELIAL LINEAGE / CHITOSAN / HYALURONIC ACID / MULTILAYER SUBSTRATE / TISSUE ENGINEERING

Аннотация научной статьи по биотехнологиям в медицине, автор научной работы — Dennaoui Hana, Chouery Eliane, Harmoush Chaza

The ease of harvesting of mesenchymal stem cells from Wharton’s jelly (WJ-MSCs), their great differentiation plasticity and low immunogenicity make them a suitable tool for allogeneic cell therapy. The aim of present study was to explore the potential of WJ-MSCs seeded on chitosan/hyaluronic acid (HA/CHI) multilayers to differentiate into endothelial-like cells. Methods In this study, we differentiate WJ-MSCs into an angiogenic lineage using polyelectrolyte multilayer film as a substrate. WJ-MSCs were cultivated on HA/CHI multilayer film and stimulated (or not) with EGM-2® culture medium. Type I collagen was used as control. mRNA and protein expression of CD31, vascular endothelial growth factor-receptor 2 (VEGF2) and vascular endothelial (VE)-cadherin, along with Dil-acetylated low-density lipoprotein-uptake and von Willebrand Factor protein expression were performed. Results The isolated MSCs showed typical fibroblast-like morphology. We have shown that WJ-MSCs express endothelial markers after 15 days of culture in EGM-2® medium. The mRNA levels were higher on CHI/HA than on collagen for CD31 and KDR, with only KDR increase being statistically significant. At the protein level, a trend for increase in KDR and CDH5 levels was also shown on CHI/HA relative to collagen. Moreover, the WJ-MSCs seeded on CHI/HA showed a high fluorescence specific to von Willebrand factor after endothelial differentiation for 15 days. Conclusion We report here a new biocompatible coating allowing differentiation of WJ-MSCs into endothelial-like cells. This substrate opens new routes in tissue engineering to design allogeneic vascular grafts.

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Текст научной работы на тему «ENDOTHELIAL DIFFERENTIATION OF WHARTON’S JELLY-DERIVED MESENCHYMAL STEM CELLS SEEDED ON CHITOSAN/HYALURONAN MULTILAYER FILMS»

Cellular Therapy and Transplantation (CTT). Vol. 9, No. 4, 2020 doi: 10.18620/ctt-1866-8836-2020-9-4-59-67 Submitted: 25 August 2020, accepted: 14 November 2020

Endothelial differentiation of Wharton's Jelly-derived mesenchymal stem cells seeded on chitosan/hyaluronan multilayer films

Hana Dennaoui ', Eliane Chouery 2, Chaza Harmoush 1

1 Laboratory of Applied Biotechnology: Biomolecules, Biotherapies and Bioprocesses, AZM Centre for Biotechnology Research and its Applications, Doctoral School of Science and Technology, Lebanese University, Tripoli, Lebanon

2 Medical Genetics Unit, Faculty of Medicine, Saint Joseph University (USJ), Mar Mikhael, Beirut, Lebanon

Dr. Hana Dennaoui, Laboratory of Applied Biotechnology: E-mail: hana.dennaoui@hotmail.com

Biomolecules, Biotherapies and Bioprocesses, AZM Centre

for Biotechnology Research and its Applications, Doctoral

School of Science and Technology, Lebanese University,

El Mitein St, Tripoli, Lebanon

Citation: Dennaoui H, Chouery E, Harmoush C. Endothelial differentiation of Wharton's Jelly-derived mesenchymal stem cells seeded on chitosan/hyaluronan multilayer films. Cell Ther Transplant 2020; 9(4): 59-67.

Summary

The ease of harvesting of mesenchymal stem cells from Wharton's jelly (WJ-MSCs), their great differentiation plasticity and low immunogenicity make them a suitable tool for allogeneic cell therapy. The aim of present study was to explore the potential of WJ-MSCs seeded on chitosan/hyaluronic acid (HA/CHI) multilayers to differentiate into endothelial-like cells.

Methods

In this study, we differentiate WJ-MSCs into an angio-genic lineage using polyelectrolyte multilayer film as a substrate. WJ-MSCs were cultivated on HA/CHI multilayer film and stimulated (or not) with EGM-2® culture medium. Type I collagen was used as control. mRNA and protein expression of CD31, vascular endothelial growth factor-receptor 2 (VEGF2) and vascular endothelial (VE)-cadherin, along with Dil-acetylated low-density lipoprotein-uptake and von Willebrand Factor protein expression were performed.

Results

The isolated MSCs showed typical fibroblast-like morphology. We have shown that WJ-MSCs express en-dothelial markers after 15 days of culture in EGM-2® medium. The mRNA levels were higher on CHI/HA

than on collagen for CD31 and KDR, with only KDR increase being statistically significant. At the protein level, a trend for increase in KDR and CDH5 levels was also shown on CHI/HA relative to collagen. Moreover, the WJ-MSCs seeded on CHI/HA showed a high fluorescence specific to von Willebrand factor after endothelial differentiation for 15 days.

Conclusion

We report here a new biocompatible coating allowing differentiation of WJ-MSCs into endothelial-like cells. This substrate opens new routes in tissue engineering to design allogeneic vascular grafts

Keywords

Mesenchymal stem cells, Wharton's jelly, differentiation, endothelial lineage, chitosan, hyaluronic acid, multilayer substrate, tissue engineering.

Introduction

Cardiovascular diseases are the leading cause of human morbidity worldwide. Systemic atherosclerosis is considered to be one of the most common, severe, and life-threatening conditions [1]. Despite a variety of pharmaceutical and surgical treatment approaches to this pathology, they frequently lack the desired effectiveness. Since the beginning of the 21st century, development of endovascular techniques has changed clinical indications and operative techniques in all the areas of vascular surgery. The classical bypass surgery, which required arterial substitutes, is now less used [2]. Hence, the goal of vascular research should be centered not on the search for an ideal arterial substitute, but on improving minimally invasive techniques such as cell therapy and regenerative medicine, aiming to develop new treatments of atherosclerosis in the near future.

Stem cell therapy is a novel and promising strategy which potentially is more effective than single-agent drug therapies for many diseases [3, 4]. Stem cells function in the repair of injured tissues in two ways: by secretion of related cytokines [5], or by differentiating into the cell types at the site of injury, in order to exert its original function [6].

Multipotent mesenchymal stem cells (MSCs) which possess self-renewal potential and can differentiate into various cell types, such as osteoblasts, chondrocytes or adipocytes [7], may be isolated from adult tissues, including bone marrow, adipose tissue, and birth-associated tissues, such as placenta, umbilical cord, cord blood or amnion. MSCs are identified by three characteristics: (1) adherence to the culture dishes; (2) differentiation into osteoblasts, chondroblasts and adipo-cytes, and (3) expression of specific surface markers (CD90, CD105, CD73 and CD44), as well as lacking expression of several other markers including CD34 and HLA-DR [8-10].

Wharton's jelly-derived MSCs (WJ-MSCs) have a high proliferation rate; they do not show any teratogenic, or carcinogenic behavior in case of transplantation [11]. The bone marrow and adipose tissue, among others, are, generally, used as sources of MSCs [7, 12]. Recent findings have shown that MSCs from human umbilical cord have advantages such as large numbers on harvest, strong proliferation and differentiation capacity and low immunogenicity compared to MSCs from the bone marrow [13].

Porous scaffolds prepared from natural polysaccharides are promising matrices for mimicking the in vivo ECM (extracellular matrix), since they resemble glycosaminoglycans (GAGs), which are essential ECM components [14]. Hyaluronic acid (HA) is a natural anionic polymer found in synovial fluid, skin, and cartilage, being among the major GAG components of brain ECM [15]. HA is used for diverse biomedical applications, due to its biocompatibility and water binding capacity [16, 17]. Due to its remarkable hydrody-namic characteristics, particularly in terms of viscosity and ability to retain water, HA plays a significant role in assembly of extracellular and pericellular matrices by regulating their porosity and malleability [18].

The negative charge of HA hinders cell adhesion. Therefore, it is blended with other biomaterials to promote cell attach-

ment [19]. Chitosan (CHI) is a widely used natural cation-ic polymer derived from crustacean shells that resembles GAGs, and has broad tissue engineering applications in view of its biocompatibility, biodegradability, hydrophilicity, low cost and availability [17]. The cationic nature of chitosan allows it to interact with negatively charged polymers and to form a polyelectrolyte complex (PEC) through ionic bonding [20].

Endothelial cells are one of the major components of the vessel wall, and these cells are important contributors to vascular tissue repair and regeneration [21]. The aim of present study was to explore the potential of WJ-MSCs seeded on HA/CHI multilayers to differentiate into endothelial-like cells, by identifying and evaluating endothelial cell morphology, and studying endothelial cell-specific gene expression at mRNA and protein levels.

Materials and methods

Polyelectrolytes multilayer films and collagen film

Hyaluronic acid solution (0.2 mg/mL in NaCl 0.15 M) and chitosan solution (0.2 mg/mL in NaCl 0.15 M/HCl 2mM) were used to produce the polyelectrolyte multilayers. Reagents were obtained from commercial sources and used without any further purification. Chitosan low-molecular weight and hyaluronan (200 kDa) were obtained from Sigma Aldrich (Germany). Each experiment was preceded by a cleaning step of the cover glasses as follows: 15 min with 1% sodium dodecyl sulfate (Sigma Aldrich, Germany) at 100°C, extensive ultrapure water rinse, 15 min at 100°C with 0.1 M HCl and, finally, cover glasses were thoroughly rinsed with ultrapure water. Coverslips were incubated in CHI solution for 5 min, thoroughly washed in NaCl (0.5 M) and then incubated in HA solution for 5 min. (CHIHA)10 films were built up after 20 alternate depositions of polycation and polynion layers. The type I collagen (100 ^g/mL, purchased from BD Biosciences, France) was used as positive control for cellular adhesion. The collagen solution was added to the coverslips and incubated for 1 hour at room temperature. Then, the solution was carefully aspirated and the surface of glasses was rinsed 3 times with serum-free a-MEM.

Stem cell and mature endothelial cell isolation and culture

Fresh human umbilical cords were obtained after full-term births with informed consent using the guidelines approved by the Hanan Hospital. Umbilical cord vessels were removed manually from cord segments, and the exposed Whar-ton's jelly was cut into very small pieces or explants. These explants were cultured in a-MEM (Lonza, Belgium) supplemented with 10% decomplemented fetal bovine serum (FBS), 2 mM L-glutamine, 100 IU/mL Penicillin/streptomycin and 2.5 mg/mL Fungizon® (Fisher, France) at 37°C and in 5% CO2. At the fourth passage, WJ-MSCs were characterized by flow cytometry (FACSCalibur; BD Bioscience), as previously described [22], by assessing the expression of CD73, CD90, CD44, CD105, CD34, CD45 and HLA-DR, and then used in our experimental procedure.

Human umbilical vein endothelial cells (HUVECs) were isolated according to the method of Jaffe et al. [23]. Briefly, the umbilical cords were washed in HBSS solution and HUVECs were extracted from umbilical cords veins using Trypsin. Then HUVECs were cultured at 37°C in 5% CO2 in 25 cm2 tissue-culture-treated flask (suitable for cell attachment and growth) in complete medium. The medium consisted of an equal mixture of M199/RPMI 1640 media supplemented with 20% human serum albumin, 2 mM L-glutamine, 20 mM HEPES, 100 IU/mL Penicillin, 2.5 mg/mL Fungizon®, being replaced every two days. The cells were used at the second passage culture and were seeded at 3x103 cells/cm2.

Endothelial cell differentiation

WJ-MSCs were seeded in 6-well plates at 3000 cells/cm2 on CHI/HA or on COL-I coated glass substrates in a-MEM for 2 days. The unstimulated cells were then incubated in the complete Endothelial Basal Medium (EBM-2, Lonza®), without growth factor supplements, whereas the stimulated were are incubated in complete Endothelial Growth Medium (EGM2, Lonza® supplemented with EPCs-differentiating medium) for 2 weeks.

As a negative control, the cells were cultured on glass in endothelial basal medium (EBM-2, Lonza®) supplemented with 0.5% FBS. The culture medium was changed every 2 days. The cells cultured on both surfaces (glass and PEMs architectures) were observed daily by phase contrast microscopy (Leica) to check their morphology.

Evaluation of endothelium-specific mRNA markers

Transcript levels of CD31 (PECAM-1 platelet endothelial cell adhesion molecule), CDH5 (Vascular endothelial Cadherin) and KDR (VEGFR-2 vascular endothelial growth factor 2) genes were quantified by real-time qPCR. Total RNA were isolated with RNeasy mini kit (Qiagen, GmbH, Hilden, Germany) according to the manufacturer's instructions. Complementary DNA synthesis was performed with 350 ng total RNA using iScript cDNA synthesis kit (Bio-Rad, USA). Real-time qPCR was conducted as described previously [24]. As a positive control, RNA isolated from human umbilical vein endothelial cells (HUVECs) was used. These cells were isolated from the umbilical cord veins and cultured in M199/ RPMI medium.

Measurement of gene expression was performed in duplicate; a non-template blank served as a negative control. qPCR was carried out using iQ SYBR® Green Supermix (Bio-Rad®) and in-home designed primers (using Primer3) for human CD-31, VE-cadherin, VEGF-R2 and ribosomal protein. Forward and reverse primers (Eurogenetec) were as follows:

CD31: 5'-ATGATGCCCAGTTTGAGGTC-3'; 5'-ACGTCTTCAGTGGGGTTGTC-3',

KDR: 5'-GTGACCAACATGGAGTCGTG-3'; 5'-TGCTTCACAGAAGACCATGC-3';

CDH5: 5'-CCTACCAGCCCAAAGTGTGT-3'; 5'-GACTTGGCATCCCATTGTCT-3';

RPS29: 5'-TCATCTTCCAGCCCAAATTC-3'; 5'-CTTGAACGGTTACCACCTCA-3'

PCR was performed with MyCycler™ Personal Thermal Cycler (Bio-Rad®). Cycling parameters were 3 min at 95°C; 40 cycles of 3 min at 60°C for CD31, VEGF-R2 and RP29 and 62°C for VE-cadherin and 1 min at 72°C. The results were normalized to the housekeeping gene for S29 ribosomal protein. Analyses and fold differences were determined using the comparative CT method. The fold changes were calculated from the AACT values using the formula 2-AACT, and the data were normalized relative to the reference gene values and then expressed as percentage of values obtained in HU-VEC for each assayed mRNA.

Detection of endothelium-specific protein markers

Total proteins from cultured cells were prepared as previously described [26]. 25 ^g proteins from each sample were heated at 95°C for 5 min in Laemmli sample buffer (BioRad, USA), and the total proteins were separated in acrylamide gel (10% for VEGF-R2, Vascular endothelial growth factor receptor 2, and 7% for CD31 and VE-cadherin. After electrophoresis, the gels were blotted to nitrocellulose membranes. GAPDH was used as loading control. Western blots were performed by using primary antibodies for endothelial VEGFR2 markers with 1/1000 milk/TBST (Tris-Buffered Saline Tween 20 0.5% from Cell Signaling Technology, UK); VE-cadherin with 1/1000 BSA (Bovine Serum Albumin/TBST from Ab-cam, USA); CD31 with 1/1000 BSA/TBST (Dako, France). The membranes were blocked with the blocking buffer TBS (Tris Buffer Saline) for 1h at room temperature and incubated with primary antibodies under gentle shaking at 4°C overnight. After extensive washing by TBS, the membranes were incubated for 1 h at room temperature with secondary antibodies conjugated to horseradish peroxidase (HRP). HRP activity was detected by enhanced chemiluminescence (ECL, Santa Cruz Biotechnology, USA). Santa Cruz Luminol Reagent A & B associated, will be oxidized by HRP in presence of hydrogen peroxide emitting the light. Densitometry of the obtained bands was estimated by ImageJ software.

Evaluation of endothelial-like cells functionality in terms of LDL-uptaking assay

Low-density lipoprotein (LDL)-uptake assay was performed as described previously. At day 15, WJ-MSCs seeded on collagen and PEMs architectures were incubated for 4 h at 37°C in RPMI 1640 without phenol red supplemented with 0.8 ^g/ mL Dil-Ac-LDL (Tebu-bio, France) labeled with rhodamine. Cells were washed with RPMI 1640 without phenol red to remove Dil-Ac-LDL. They were then fixed with 4% paraformaldehyde and nuclei were counterstained using 4',6-dia-midino-2-phenylindole DAPI. The cells were observed using fluorescence microscopy (Leica microscope, *40) after using the appropriate excitation and emission filters for Rhodamin B (554nmEx/571nmEm).

Von Willebrand Factor (vWF) immunostaining

After 15 days of endothelial differentiation, the WJ-MSCs seeded on collagen and PEMs architectures were analyzed to assess vWF expression. The cells were fixed by 4% paraformaldehyde, permeabilized with PBS/Triton X-100 (0.1%) for 15 min, blocked with 1% BSA and stained by

murine anti-vWF (1/100 Dako, France). After two washes with PBS, the appropriate secondary antibody labeled with Alexa-Fluor-488 (diluted at 1/100) was incubated for 30 min at 37°C. The cells were then observed by fluorescence microscopy (Zeiss microscopy, x 630 magnification) using the (485Ex/538Em) spectral line.

Statistical analysis

Data were presented as a mean ± SEM for each condition. Each experiment was repeated independently three times (n=3). Pairwise comparisons were performed using one-factor ANOVA with Fisher correction (Stat view IVs, Abacus Concepts Inc., Berkley, CA). Differences were considered significant for p (rejection level of the null-hypothesis of equal means) values < 0.05.

Results and discussion

Characterization of WJ-MSCs

Morphological characterization of MSCs (4th passage) was performed according to the criteria defined by the International Society for Cellular Therapy [25]. MCSs derived from WJ of three umbilical cords displayed a homogeneous fibro-blast-like morphology. Cells were analyzed regarding the expression of specific molecular markers by Fluorescein-Ac-tivated Cell Sorting analysis and showed that WJMSCs and BM-MSCs were positive for CD105, CD73, and CD90, and negative for CD45, CD34, CD86, and HLA-DR. These data revealed that WJ-MSCs used in this study showed the typical MSC characteristics (Data not shown).

Evaluation of endothelial markers expression at the mRNA and protein levels

In order to evaluate the effect of different adhesion matrices on differentiation of WJ-MSCs in endothelial-like cells, we measured the expression of endothelial markers by q-PCR and Western Blot. The three endothelial-specific molecules CD31, VE-cadherin and VEGF-R2 (KDR) are known to play an important role in the endothelium maturation during angiogenesis process [26]. CD31, also known as platelet endothelial cell adhesion molecule-1 (PECAM-1), is a type I integral membrane glycoprotein that is expressed at high levels on early and mature endothelial cells, platelets, and most leukocyte subpopulations. PECAM-1 is known to have various roles in vascular biology including angiogenesis, platelet function, and thrombosis [27]. VEGF-R2 is expressed on vascular endothelial cells and lymphatic endothelial cells; it regulates vascular endothelial function. VEGF is an important growth factor for the endothelial differentiation [28]. The endothelial-specific cadherin, vascular endothelial cad-herin (VE-cadherin) is required for vascular genesis and the repair of damaged vessels [29].

The mRNA and protein levels of the three endothelial specific markers CD31, VEGF-R2 (KDR) and VE-cadherin were analyzed by real-time qPCR and Western blot (Figures 1 and 2). Relative expression of the three molecules was analyzed at mRNA and protein levels, and expressed relative to appropriate HUVEC values. WJ-MSCs seeded on CHI/HA or

collagen and incubated in EBM-2 did not express the three markers at the protein level whereas their expression at the mRNA level was barely detectable (<1% of the levels found in HUVECs for CD31 and CDH5). In WJ-MSCs incubated in EGM-2 for 15 days, mRNA level was higher on CHI/ HA than on collagen for CD31 and KDR (increase by 67%, and 79%, respectively). However, only the KDR increase was statistically significant. At the protein level, KDR expression was higher on CHI/HA relative to collagen (45% increase), but this difference was not statistically significant. CD31 protein levels were unchanged between collagen and CHI/ HA, whereas CDH5 level was higher on CHI/HA relative to collagen (4% increase), and the difference was statistically significant. The fold change between collagen and CHI/HA at mRNA level was more important than fold change at protein level. After 15 days of differentiation, the transcription of endothelial genes give rise to high levels of mRNA from these genes. The translation process might take more culture time, to produce similar levels of proteins.

Higher mRNA and protein expression of these three markers in differentiated WJ-MSCs seeded on CHI/HA could contribute to more pronounced endothelial differentiation as compared with differentiated WJ-MSCs seeded on collagen. However, collagen is a recommended surface, allowing MSCs chondrogenic and osteogenic differentiation after 21 days [30]. In our report, we have not detected expression of VEGF-R2 protein on the collagen surface; maybe we needed more than 15 days to notice the translation of VEGF-R2 gene.

The capacity to differentiate towards endothelial pheno-type is a characteristic of mesenchymal stem cells [30-32], and our results showed that WJ-MSCs express endothelial markers at mRNA and protein levels after 15-day cultures in presence of endothelial growth factors. However, the main purpose of this study was to evaluate endotheliogenic potential of WJ-MSCs seeded onto CHI/HA scaffolds. First, we verified the endothelial potential of WJ-MSCs in monolay-er culture conditions both in proliferation (data not shown) and differentiation media. In proliferation medium, no en-dothelial differentiation was observed during the entire experimental time (15 days), further confirming the stem-cell origin of isolated cells. In differentiation medium, RT-PCR and Western Blot confirmed a better endothelial potential of these cells on CHI/HA.

Our choice of the CHI/HA scaffold was based on some studies that demonstrated the efficacy of this natural scaffold in enhancing hMSCs differentiation into stromal cells. hMSCs were induced to differentiate to chondrogenic, osteogenic, and adipogenic phenotypes [33]. Recent studies have shown the potential of WJ-MSCs to differentiate towards cardiomy-ocytes using CHI/HA scaffolds [34]. In our study, we have demonstrated that WJ-MSCs are able to differentiate into endothelial cells on CHI/HA films. Therefore, we can deduce that a combination of these cells with this natural scaffold is advantageous for cardio-vascular tissue engineering. Same conclusive results were observed in healing of diabetic skin wound by the proliferation and differentiation of human umbilical cords mesenchymal stem cells (hUCMSCs) on the collagen/chitosan laser drilling acellular dermal matrix (CCLDADM) scaffold, a natural scaffold used in vivo [35].

Figure 1. Investigation of endothelial cell markers at the mRNA level

Expression of the endothelial markers: CD31, CDH5 and KDR at the mRNA level was assessed in HUVECs endothelial-life cells seeded on collagen and CHI/HA in differentiation medium (EGM2) for 15 days. Results show the mRNA level normalized to the reference gene mRNA RP29 level and expressed relative to the mRNA level in HUVECs (set as 100) and non-treated cells (data not shown). Results represent the average of 3 independent experiments ± SEM.

Figure 2. Studies of endothelial markers at the protein level

CD31, VEcadherin and VEGF-R2 blot quantifying for stimulated and unstimulated WJMSCs seeded on different culture surfaces after 15 days. Western blot normalization was performed to the expression of GAPDH. The expression in HUVECs was assumed for 100% (relative protein level=1.0). Results were expressed as the mean of 3 independent experiments ± SEM. ***: p< 0,001.

Evaluation of endothelial-like cells functionality by LDL uptake assay

LDL-uptake assay is applied for detection of functional en-dothelial cells. WJMSCs, when seeded on CHI/HA and collagen, captured DiIAcLDL to the cytoplasm after 4 hour-incubation in RPMI medium supplemented with DiI-Ac-LDL. However, MSCs were unable to uptake DiI-Ac-LDL after culturing in the growth medium as negative controls (Fig. 3). These results confirm that, after two weeks, WJ-MSCs seeded on CHI/HA and collagen exhibit endothelial cell phenotype. In this respect, Gaffney et al. investigated lipoprotein uptake by means of flow cytometry and showed that the cells in a G2/M (mitosis) phase incorporated about 45% more Dil-Ac-LDL than those in a G1/S (latency) phase [36]. Higher Dil-Ac-LDL uptake of endothelium-like cells on PEMs suggests that more cells are in the G2/M phase on PEMs, a feature of higher proliferation.

Detection of endothelial-specific marker expression: vWF (von Willebrand Factor) by immunocy-tochemistry

Von Willebrand adherence factor (vWF) protein contributes to platelet function by mediating the initiation and progression of thrombus formation at the sites of vascular injury. Moreover, novel findings have been obtained on the link between regulation of VWF multimer size and microvascu-lar thrombosis. This progress in basic research has provided critical information to define with greater precision the role of vWF in vascular biology and pathology, including its possible involvement in the onset of atherosclerosis and its acute thrombotic complications. Therefore we have used the expression of vWF as a functionality test of our endotheli-al-like cells [37]. The cells were examined for expression of endothelial-specific marker (vWF) by immunocytoche-mistry.

WJ-MSCs seeded on CHI/HA showed a high fluorescence specific to this marker after endothelial differentiation for 15 days. MSCs did not show any positive signal after they were cultured in the growth medium (EBM2) on the same scaffold, as negative controls. On collagen layer, the cells were not marked, that was predicted because they needed more culture time to express vWF protein (Fig. 4).

These promising results showed the possibility to combine the use of WJ-MSCs and CHI/HA films aiming for vascular tissue engineering, by evaluating the capacity of WJ-MSCs to differentiate into smooth muscle cells on CHI/HA, coating the surface of alginate hydrogels with CHI/HA films, and enrolling them in order to form a tubular vascular graft.

These promising data showed that the combination of WJ-MSCs and CHI/HA may lead to brilliant results, regarding endothelial differentiation and angiogenesis. One may recommend using of these cells and materials for vascular tissue engineering and regeneration therapy. More studies can be done to evaluate the capacity of WJ-MSCs to differentiate into smooth muscle cells on CHI/HA, to coat the surface of alginate hydrogels with CHI/HA films and to enroll them, in order to form a tubular vascular graft.

Collagen CHI/HA

Figure 3. LDL-Uptake assay

WJ-MSCs cellular uptake of labeled acetylated LDLs. Double immunofluorescence of nuclei (blue) and for DI-Ac-LDLs (red) for unstimulated (a, b) and stimulated (c, d) WJMSCs after 15 days of culture on collagen and CHI/HA. Internalized labels were detected by Leica fluorescence microscopy (objective *40 oil).

Collagen CHI/HA

Figure 4: vWF immunostaining

Double immunofluorescence staining for nuclei (blue), and for prothrombogenic von Willebrand Factor for stimulated (a, b) and unstimulated (d, e) WJ-MSCs after 15 days of culture on collagen and CHI/HA (Zeiss Microscope, objective*63 oil). N=3.

Conclusion

These first quite encouraging results showed that it is possible to obtain CEs-like in a non-traumatic way (from Wharton's jelly of human umbilical cords) and in a short time (15 days). Our technique, based on the use of polyelectrolyte films, could therefore be used in the field of vascular engineering for the development of functional vascular substitutes comprising an endothelium resulting from differentiation of mesenchymal stem cells, which would limit the risks of graft rejection and could be applied to patients who require vessel replacement.

Acknowledgements

The authors would like to thank Al Hanan Hospital for providing the umbilical cords used in our researches and Azm & Saadeh society for funding this work.

The authors have no conflicts of interest to declare.

Ethical Statement: The research work was approved by the ethical committee of the Lebanese University, Centre Azm for research in Applied Biotechnology and the ethical Committee of Al Hanan Hospital-Tripoli, Lebanon.

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Эндотелиальная дифференцировка мезенхимных стволовых клеток из соединительной ткани пуповины (желе Вортона) на многослойных пленках из хитозана/гиалуронинана

Хана Деннауи Элиана Шуэри 2, Шаза Хармуш 1

1 Лаборатория прикладной биотехнологии: биомолекулы, биотерапия и биопроцессы, научно-прикладной центр биотехнологии AZM, докторская школа науки и технологий, Ливанский университет, Триполи, Ливан

2 Отделение медицинской генетики, факультет медицины, университет Св. Иосифа (USJ), Мар-Микаэл, Бейрут, Ливан

Резюме

Простота заготовки мезенхимных стволовых клеток из желе Вортона (МСК-ЖВ), выраженная пластичность дифференцировки и низкая иммуноген-ность делают их удобным средством аллогенной клеточной терапии. Целью данного исследования было изучение способности к дифференцировке в эндотелиоподобные клетки МСК-ЖВ, культивированных на гиалуронан-хитозановых (ГХ) многослойных носителях.

Материалы и методы

В этой работе мы проводили дифференцировку МСК-ЖВ в ангиогенном направлении с применением полиэлектролитной многослойной пленки в качестве субстрата. МСК-ЖВ культивировали на ГХ-многослойной пленке и стимулировали факторами культуральной среды ЕОМ-2®. Коллаген типа I использовали в качестве контрольного субстрата. Определяли экспрессию специфических мРНК, а именно: CD31, рецептора фактора роста сосудистого эндотелия типа 2 (УЕОБ2) и эндотелиально-го сосудистого кадхерина (УЕ), наряду с уровнями абсорбции Dil-ацетилированного липопротеина низкой плотности и экспрессией белкового фактора Виллебранда.

Результаты

Выделенные МСК-ЖВ имели типичную морфологию фибробластоподобных клеток. Уровни мРНК, кодирующих CD31 и КЛК. были выше после культивирования на ГХ-субстрате, нежели на колла-геновом покрытии, при достоверном повышении экспрессии KDR. На уровне белков, показана тенденция к повышению уровней KDR и CDH5 после инкубации на ГХ-субстрате, по сравнению с коллагеном. Кроме того, МСК-ЖВ, культивированные на ГХ, имели высокие уровни экспрессии эндотели-альных маркеров после 15 суток культивирования в среде ЕОМ-2®.

Выводы

В данной работе мы сообщаем о новом биосовместимом субстрате, который способствует диффе-ренцировке МСК-ЖВ в эндотелиоподобные клетки. Разработка этого субстрата является новым подходом в тканевой инженерии для создания аллоген-ных сосудистых трансплантатов.

Ключевые слова

Мезенхимные стволовые клетки, желе Вортона, диф-ференцировка, эндотелий, хитозан, гиалуроновая кислота, многослойный субстрат, тканевая инженерия.

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