Shen Bin Journal Club
What is MSCs? Mesenchymal stem cells (MSCs) are multipotent stromal cells that can differentiate into a variety of cell types [1] including: osteoblasts (bone cells) [2] chondrocytes (cartilage cells) [3] myocytes (muscle cells)[4] and adipocytes (fat cells). 1.Nardi, N. Beyer et al. Stem Cells Oni OO et al. J Bone Joint Surg Am Brighton CT et al. J Orthop Trauma Pittenger et al. Science. 1999
CHARACTERISTICS Morphology Fibroblast-like Detection Express :CD73, CD90 and CD105 Lacking the expression: CD11b, CD14, CD19, CD34, CD45, CD79a and HLA-DR Self-renewal and differentiation capacity Great capacity for self-renewal osteoblasts, adipocytes, and chondrocytes, myocytes neurons, hepatocyte and beta-like cells. Immunomodulatory effects avoid allorecognition ○ interfere with dendritic cell and T-cell function ○ secreting cytokines Jiang Y et al. Nature, 2002 Franco Lambert AP et al. Differentiation Engler AJ et al. Cell Ryan JM et al. Journal of Inflammation Ryan JM et al. Clinical & Experimental Immunology Phinney DG et al. Stem Cells. 2007
MEDICAL USE Intravenous transplantation systemic diseases like graft versus host disease and sepsis Increase the local concentration of cells inflammatory bowel disease Direct injection or placement of cells into a site in need of repair orthopedic applications chondral defects …… Heirani-Tabasi A et al. Journal of Genes and Cells Manieri NA et al. Current Opinion in Gastroenterology Fischer UM et al. Stem Cells and Development Wakitani S et al. Journal of Tissue Engineering and Regenerative Medicine. 2007
IMMUNOMODULATION MSCs effect proliferation, maturation and cytokine secretion by different immune cells. NK cells, Natural Killer Cells; iDCs, Immature Dendritic Cells; APCs, Antigen Presenting Cells.
CELL AND ORGAN TRANSPLANTATION
Graft vs. Host Disease HSC transplantation GVHD Corticosteroids MSCs from the donor and controls inhibited patient lymphocyte proliferation by 90% before and after transplantation
REGENERATIVE MEDICINES Transdifferentiation of MSCs to β cells Small molecular chemicals, growth factors Genetic modifications, pdx1 Hepatocytes cardiac tissues cardiac myocytes Ectodermal differentiation neurons, and astrocytes
GENE CARRIERS Genetic modifications of MSCs have been performed to improve the MSC efficacy in tissue repair/regeneration Secretion of growth factors neurotropic factors Liver tp, HGF, BDNF, IGF-1 and VEGF cytoprotective effects and lead to tissue repair
CHALLENGES TO MSC-BASED THERAPY poor delivery of MSCs spontaneous malignant transformation of MSCs unwanted differentiation MSC differentiation to myofibroblasts instead of hepatocytes is unwanted and leads to worsening of liver injury
CLINICAL TRIALS