Enhanced chondrogenesis of mesenchymal stem cells over silk fibroin/chitosan-chondroitin sulfate three dimensional scaffold in dynamic culture condition
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Agrawal, Parinita
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Natl Inst Technol, Dept Biotechnol & Med Engn, Rourkela, Odisha, IndiaNatl Inst Technol, Dept Biotechnol & Med Engn, Rourkela, Odisha, India
Agrawal, Parinita
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Pramanik, Krishna
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Vishwanath, Varshini
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Natl Inst Technol, Dept Biotechnol & Med Engn, Rourkela, Odisha, IndiaNatl Inst Technol, Dept Biotechnol & Med Engn, Rourkela, Odisha, India
Vishwanath, Varshini
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Biswas, Amit
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Bissoyi, Akalabya
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Patra, Pradeep Kumar
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Pandit Jawahar Lal Nehru Mem Med Coll, Dept Biochem, Raipur, Chhattisgarh, IndiaNatl Inst Technol, Dept Biotechnol & Med Engn, Rourkela, Odisha, India
Patra, Pradeep Kumar
[3
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[1] Natl Inst Technol, Dept Biotechnol & Med Engn, Rourkela, Odisha, India
[2] Natl Inst Technol, Dept Biomed Engn, Raipur, Chhattisgarh, India
[3] Pandit Jawahar Lal Nehru Mem Med Coll, Dept Biochem, Raipur, Chhattisgarh, India
Chondroitin sulfate (Ch) is one of the main structural components of cartilage tissue, therefore, its presence in tissue engineered scaffold is expected to enhance cartilage regeneration. Previously, silk fibroin/chitosan (SF/CS) blend was proven to be a potential biomaterial for tissue development. In this study, the effect of Ch on physicochemical and biological properties of SF/CS blend was investigated and scaffolds with 0.8 wt% Ch was found to be favorable. The scaffolds possess pore size of 37-212 mu m, contact angle 46.2-50.3 degrees, showed controlled swelling and biodegradation. The biocompatibility of scaffold was confirmed by subcutaneous implantation in mouse. Human mesenchymal stem cells (hMSCs) seeded scaffolds cultured under spinner flask bioreactor promoted cell attachment, proliferation, distribution, and metabolic activity in vitro. The histology and immunofluorescence studies revealed that combined effect of Ch and dynamic condition resulted in higher glycosaminoglycan secretion and native cartilage type matrix synthesis in comparison to SF/CS scaffolds used as control. Higher expression of collagen-II, Sox9, aggrecan and decrease in collagen-I expression represented by quantitative polymerase chain reaction study confirmed the progression of chondrogenic differentiation. This study successfully demonstrates the potentiality of SF/CS-Ch scaffold for hMSCs recruitment and redirecting cartilage tissue regeneration with enhanced chondrogenesis. (C) 2018 Wiley Periodicals, Inc.
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Case Western Reserve Univ Hosp, Sch Med, Div Rheumatol, Cleveland, OH 44106 USACase Western Reserve Univ Hosp, Sch Med, Div Rheumatol, Cleveland, OH 44106 USA
Deal, CL
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Moskowitz, RW
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Case Western Reserve Univ Hosp, Sch Med, Div Rheumatol, Cleveland, OH 44106 USACase Western Reserve Univ Hosp, Sch Med, Div Rheumatol, Cleveland, OH 44106 USA
机构:
Case Western Reserve Univ Hosp, Sch Med, Div Rheumatol, Cleveland, OH 44106 USACase Western Reserve Univ Hosp, Sch Med, Div Rheumatol, Cleveland, OH 44106 USA
Deal, CL
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Moskowitz, RW
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Case Western Reserve Univ Hosp, Sch Med, Div Rheumatol, Cleveland, OH 44106 USACase Western Reserve Univ Hosp, Sch Med, Div Rheumatol, Cleveland, OH 44106 USA