A 3D Porous Gelatin-Alginate-Based-IPN Acts as an Efficient Promoter of Chondrogenesis from Human Adipose-Derived Stem Cells

Author:

Dinescu Sorina1,Galateanu Bianca12,Radu Eugen3,Hermenean Anca2,Lungu Adriana4,Stancu Izabela Cristina4,Jianu Dana56,Tumbar Tudorita7,Costache Marieta1

Affiliation:

1. Department of Biochemistry and Molecular Biology, University of Bucharest, 91-95 Splaiul Independentei, 050095 Bucharest, Romania

2. Institute of Life Sciences, Vasile Goldis Western University of Arad, 86 Rebreanu, 310414 Arad, Romania

3. Molecular Biology and Pathology Research Lab “Molimagex”, University Hospital Bucharest, 169 Splaiul Independentei, 050098 Bucharest, Romania

4. Advanced Polymer Materials Group, University Politehnica of Bucharest, 1-7 Gheorghe Polizu Street, District 1, 011061 Bucharest, Romania

5. Proestetica Medical S.R.L., 38-40 T. Stefan Street, 011658 Bucharest, Romania

6. International Society of Regenerative Medicine and Surgery, 38-40 T. Stefan Street, 011658 Bucharest, Romania

7. Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA

Abstract

Cartilage has limited regeneration potential. Thus, there is an imperative need to develop new strategies for cartilage tissue engineering (CTE) amenable for clinical use. Recent CTE approaches rely on optimal cell-scaffold interactions, which require a great deal of optimization. In this study we attempt to build a novel gelatin- (G-) alginate- (A-) polyacrylamide (PAA) 3D interpenetrating network (IPN) with superior performance in promoting chondrogenesis from human adipose-derived stem cells (hADSCs). We show that our G-A-PAA scaffold is capable of supporting hADSCs proliferation and survival, with no apparent cytotoxic effect. Moreover, we find that after exposure to prochondrogenic conditions a key transcription factor known to induce chondrogenesis, namely, Sox9, is highly expressed in our hADSCs/G-A-PAA bioconstruct, along with cartilage specific markers such as collagen type II, CEP68, and COMP extracellular matrix (ECM) components. These data suggest that our G-A-PAA structural properties and formulation might enable hADSCs conversion towards functional chondrocytes. We conclude that our novel G-A-PAA biomatrix is a good candidate for prospectivein vivoCTE applications.

Publisher

Hindawi Limited

Subject

Cell Biology,Molecular Biology

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