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Mesenchymal stem cells for cartilage repair in osteoarthritis
被引:204
|作者:
Gupta, Pawan K.
[1
]
Das, Anjan K.
[1
,2
]
Chullikana, Anoop
Majumdar, Anish S.
[1
]
机构:
[1] Stempeut Res Private Ltd, Bangalore 560066, Karnataka, India
[2] Stempeut Res Malaysia Sdn Bhd, Kuala Lumpur 57000, Malaysia
来源:
关键词:
AUTOLOGOUS CHONDROCYTE TRANSPLANTATION;
BONE-MARROW;
ARTICULAR-CARTILAGE;
CHONDROGENIC DIFFERENTIATION;
STROMAL CELLS;
DEFECTS;
ADULT;
THERAPY;
KNEE;
IMPLANTATION;
D O I:
10.1186/scrt116
中图分类号:
Q813 [细胞工程];
学科分类号:
摘要:
Osteoarthritis (OA) is a degenerative disease of the connective tissue and progresses with age in the older population or develops in young athletes following sports-related injury. The articular cartilage is especially vulnerable to damage and has poor potential for regeneration because of the absence of vasculature within the tissue. Normal load-bearing capacity and biomechanical properties of thinning cartilage are severely compromised during the course of disease progression. Although surgical and pharmaceutical interventions are currently available for treating OA, restoration of normal cartilage function has been difficult to achieve. Since the tissue is composed primarily of chondrocytes distributed in a specialized extracellular matrix bed, bone marrow stromal cells (BMSCs), also known as bone marrow-derived 'mesenchymal stem cells' or 'mesenchymal stromal cells', with inherent chondrogenic differentiation potential appear to be ideally suited for therapeutic use in cartilage regeneration. BMSCs can be easily isolated and massively expanded in culture in an undifferentiated state for therapeutic use. Owing to their potential to modulate local microenvironment via anti-inflammatory and immunosuppressive functions, BMSCs have an additional advantage for allogeneic application. Moreover, by secreting various bioactive soluble factors, BMSCs can protect the cartilage from further tissue destruction and facilitate regeneration of the remaining progenitor cells in situ. This review broadly describes the advances made during the last several years in BMSCs and their therapeutic potential for repairing cartilage damage in OA.
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