Dang Quan Tran, Huynh Thao Duy, Inchingolo Francesco, Dipalma Gianna, Inchingolo Alessio Danilo, Cantore Stefania, Paduanelli Gregorio, Nguyen Kieu Cao Diem, Ballini Andrea, Isacco Ciro Gargiulo, Tran Cong Toai
University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.
Pham Ngoc Thach University of Medicine, Ho Chi Minh City, Vietnam.
Stem Cells Int. 2021 Feb 23;2021:6664697. doi: 10.1155/2021/6664697. eCollection 2021.
The articular cartilage is unique in that it contains only a single type of cell and shows poor ability for spontaneous healing. Cartilage tissue engineering which uses mesenchymal stem cells (MSCs) and adipose tissue-derived mesenchymal stem cells (AT-MSCs) is considered an attractive treatment for cartilage lesions and osteoarthritis. The establishment of cartilage regenerative medicine is an important clinical issue, but the search for cell sources able to restore cartilage integrity proves to be challenging. The aim of this study was to create cartilage grafts from the combination of AT-MSCs and collagen substrates.
Mesenchymal stem cells were obtained from human donors' adipose tissue, and collagen scaffold, obtained from human skin and cleaned from blood vessels, adipose tissues, and debris, which only preserve dermis and epidermis, were seeded and cultured on collagen substrates and differentiated to chondrocytes. The obtained chondrocyte extracellular matrix of cartilage was then evaluated for the expression of chondrocyte-/cartilage-specific markers, the Cartilage Oligomeric Matrix Protein (COMP), collagen X, alpha-1 polypeptide (COL10A1), and the Collagen II, Human Tagged ORF Clone (COL2A1) by using the reverse transcription polymerase chain reaction (RT-PCR).
Our findings have shown that the dermal collagen may exert important effects on the quality of in vitro expanded chondrocytes, leading in this way that the influence of collagen skin matrix helps to produce highly active and functional chondrocytes for long-term cartilage tissue regeneration.
This research opens up the possibility of generating cartilage grafts with the precise purpose of improving the existing limitation in current clinical procedures.
关节软骨的独特之处在于它仅包含单一类型的细胞,且自发愈合能力较差。利用间充质干细胞(MSCs)和脂肪组织来源的间充质干细胞(AT-MSCs)的软骨组织工程被认为是治疗软骨损伤和骨关节炎的一种有吸引力的方法。建立软骨再生医学是一个重要的临床问题,但寻找能够恢复软骨完整性的细胞来源颇具挑战性。本研究的目的是通过将AT-MSCs与胶原基质相结合来制备软骨移植物。
从人类供体的脂肪组织中获取间充质干细胞,并将从人类皮肤中获得、去除血管、脂肪组织和碎片(仅保留真皮和表皮)的胶原支架接种在胶原基质上并进行培养,使其分化为软骨细胞。然后,通过逆转录聚合酶链反应(RT-PCR)评估所获得的软骨细胞外基质中软骨细胞/软骨特异性标志物软骨寡聚基质蛋白(COMP)、胶原蛋白Xα-1多肽(COL10A1)和胶原蛋白II人类标记开放阅读框克隆(COL2A1)的表达。
我们的研究结果表明,真皮胶原可能对体外扩增的软骨细胞质量产生重要影响,从而表明胶原皮肤基质的影响有助于产生高活性和功能性的软骨细胞,用于长期软骨组织再生。
本研究为制备软骨移植物开辟了可能性,其确切目的是改善当前临床程序中存在的局限性。