Interleukin-17A Induced Human Mesenchymal Stem Cells Are Superior Modulators of Immunological Function Researchers modified human bone-marrow derived mesenchymal stem cells with interleukin-17A (MSC-17) to enhance T cell immunosuppression but not their immunogenicity. When co-cultured with phytohemagglutinin activated human T cells, MSC-17 were potent suppressors of T cell proliferation. [Stem Cells] Abstract miR-26a Rescues Bone Regeneration Deficiency of Mesenchymal Stem Cells Derived from Osteoporotic Mice Scientists found that miR-26a treatment could effectively improve the osteogenic differentiation capability of mesenchymal stem cells isolated from littermate-derived ovariectomized osteoporotic mice both in vitro and in vivo. [Mol Ther] Abstract Crosstalk between Bone Marrow-Derived Mesenchymal Stem Cells and Regulatory T Cells through a Glucocorticoid-Induced Leucine Zipper/Developmental Endothelial Locus-1-Dependent Mechanism The authors showed that expression of glucocorticoid-induced leucine zipper in bone marrow mesenchymal lineage cells or bone marrow-derived mesenchymal stem cells increases the production of regulatory T cells via a mechanism involving the up-regulation of developmental endothelial locus-1, an endogenous leukocyte-endothelial adhesion inhibitor. [FASEB J] Abstract Epigenetic Memory Gained by Priming with Osteogenic Induction Medium Improves Osteogenesis and Other Properties of Mesenchymal Stem Cells Researchers reported that after in vitro induction of osteogenic differentiation, mesenchymal stem cells could be reverted to a primitive stem cell population with improved cell survival, colony formation, osteogenic potential, migratory capacity and increased expression of Nanog, Oct4 and Sox2. [Sci Rep] Full Article Potent Paracrine Effects of Human Induced Pluripotent Stem Cell-Derived Mesenchymal Stem Cells Attenuate Doxorubicin-Induced Cardiomyopathy In vitro studies reveal that doxorubicin-induced reactive oxidative stress generation and cell apoptosis in neonatal rat cardiomyocytes are significantly reduced when treated with conditioned medium harvested from bone marrow mesenchymal stem cells (MSCs) or induced pluripotent stem cell-derived-MSCs. [Sci Rep] Full Article Low Molecular Weight Fraction of Commercial Human Serum Albumin Induces Morphologic and Transcriptional Changes of Bone Marrow-Derived Mesenchymal Stem Cells Bone marrow-derived mesenchymal stem cells exposed to low molecular weight fraction of commercial 5% human serum albumin (LMWF5A) exhibited an elongated phenotype with diffuse intracellular F-actin, pronounced migratory leading edges, and filopodia-like projections. In addition, LMWF5A promoted chondrogenic condensation in “micromass” culture, concurrent with the upregulation of collagen 2α1 mRNA. [Stem Cells Transl Med] Abstract | Press Release Purified Human Synovium Mesenchymal Stem Cells as a Good Resource for Cartilage Regeneration Scientists examined the colony formation and differentiation abilities of bone marrow-derived mesenchymal stem cells (MSCs) and synovium-derived MSCs isolated from the same patients. Both types of MSCs exhibited a marked propensity to differentiate into specific lineages. [PLoS One] Full Article The Effect of Quercetin on the Osteogenesic Differentiation and Angiogenic Factor Expression of Bone Marrow-Derived Mesenchymal Stem Cells Researchers showed that quercetin significantly enhanced the cell proliferation, osteogenic differentiation and angiogenic factor secretion of rat bone marrow-derived mesenchymal stem cells in a dose-dependent manner, with a concentration of 2 μM achieving the greatest stimulatory effect. [PLoS One] Full Article Runx1 and Runx3 Are Downstream Effectors of Nanog in Promoting Osteogenic Differentiation of the Mouse Mesenchymal Cell Line C3H10T1/2 To clarify the mechanism underlying the multipotency of mesenchymal stem cells and to develop a novel approach to bone regenerative medicine, the authors identified the downstream effectors of Nanog in promoting osteogenic differentiation of mouse mesenchymal cells. [Cell Reprogram] Abstract |