Abstract

Mesenchymal stem cells (MSCs) are prototypical adult stem cells, identified as an adherent, fibroblast-like population positive for CD105, CD90 and CD73, and lacking hematopietic markers. MSCs can be isolated from different adult tissues including bone marrow (BM), umbilical cord, skeletal muscle and adipose tissue. MSCs have a potent immunomodulatory function via soluble factors, including PGE2, TGF-β, indoleamine 2,3-dioxygenase (IDO), IL-10, and HGF. Treatment with MSCs can improve type 1 diabetes, liver fibrosis and arthritis via their immunomodulatory function. Intra-bone marrow bone marrow transplantation (IBM-BMT) can replace not only hemopoietic stem cells (HSCs) but also MSCs. IBM-BMT seems to be the best strategy for allogeneic BMT, and may improve aging-related diseases, including type 2 diabetes and osteoporosis. IBM-BMT has also been shown to be the most effective strategy to prevent the rejection of organ allografts. This review summarizes the immunomodulatory properties and therapeutic application of bone marrow derived-MSCs.

Highlights

  • Mesenchymal stem cells (MSCs) are multi-potent progenitor cells isolated from bone marrow (BM) [1] and other adult tissue including skeletal muscle [2], adipose tissue [3], umbilical cord [4], synovium [5], the circulatory system [6], dental pulp [7], amniotic fluid [8], fetal blood [9] and lung [10]

  • One report has suggested that allogeneic bone marrow-derived MSCs (BMMSCs) inhibit the activation, proliferation and IgG secretion of B cells in a BXSB mouse model of human systemic lupus erythematosus [61]

  • We previously reported that the transplantation of BMMSCs via Intra-bone marrowbone marrow transplantation (IBM-BMT) in conjunction with the induction of HO-1 could eradicate type 2 diabetes

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Summary

Introduction

Mesenchymal stem cells (MSCs) are multi-potent progenitor cells isolated from bone marrow (BM) [1] and other adult tissue including skeletal muscle [2], adipose tissue [3], umbilical cord [4], synovium [5], the circulatory system [6], dental pulp [7], amniotic fluid [8], fetal blood [9] and lung [10]. There have been reports indicating that MSCs secrete a variety of factors that promote tissue repair, stimulate proliferation and differentiation of endogenous tissue progenitors, and decrease inflammatory and immune reactions [24,25,26]. MSCs have been shown to modulate immunological responses via T-cell suppression [24,26,27,28].

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