Modulating Proliferation, Migration and Differentiation of Mesenchymal Stem Cells Using Interleukins

被引:0
作者
Srinivasan, Sankaranarayanan [1 ]
Ghone, Nalinkanth V. [2 ]
机构
[1] Indian Inst Technol Madras, Dept Biotechnol, Chennai 600036, Tamil Nadu, India
[2] Sri Sivasubramaniya Nadar Coll Engn, Dept Chem Engn, Kalavakkam 603110, Tamil Nadu, India
关键词
Mesenchymal stem cells; interleukins; differentiation; modulation; signaling pathways; receptors; migration; proliferation; OSTEOBLAST DIFFERENTIATION; OSTEOGENIC DIFFERENTIATION; STROMAL CELLS; CHONDROGENIC DIFFERENTIATION; CHEMOKINE RECEPTORS; BONE-FORMATION; IL-3; ACTIVATION; INHIBITION; SENESCENCE;
D O I
10.2174/011574888X313750240524115446
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal Stem Cells (MSCs) are multipotent stem cells that are obtained from various tissue sources such as bone marrow, adipose tissues, umbilical cords, dental pulps, and peripheral blood has high regenerative potential, migratory abilities, and immunosuppressive properties. These properties make them attractive candidates for tissue engineering, immunosuppressive therapies, and in vivo drug deliveries. MSCs, because of their high propensity to home in an injured tissue microenvironment, are exposed to various cytokines. These cytokines modulate the activity of MSCs to help in the regeneration of injured tissue. Interleukins are one such cytokine that is present in injured tissue microenvironment and plays significant roles in the activation, differentiation, proliferation, maturation, migration, and adhesion of not only immune cells but also MSCs. Interleukins, through both autocrine and paracrine signaling mechanisms, modulate the functioning of MSCs. This article reviews how interleukins influence MSCs by discussing their signaling pathways, their effect on differentiation and other biological effects. A comprehensive understanding of the influence of interleukins on MSCs may provide insights to manipulate improving the therapeutic potential of MSCs or reducing potential risks such as undesirable immune response and tumor formation.
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收藏
页码:546 / 564
页数:19
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