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Transforming growth factor-beta increases the expression of vascular smooth muscle cell Markers in human multi-lineage progenitor cells
Author(s) -
Hui Yang,
Lidong Zhang,
Sarah M. Weakley,
Peter H. Lin,
Qizhi Yao,
Changyi Chen
Publication year - 2011
Publication title -
medical science monitor
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.636
H-Index - 85
eISSN - 1643-3750
pISSN - 1234-1010
DOI - 10.12659/msm.881439
Subject(s) - cd146 , calponin , progenitor cell , biology , lineage markers , cd34 , mesenchymal stem cell , microbiology and biotechnology , stem cell , cellular differentiation , stem cell marker , cd44 , endoglin , endothelial stem cell , transforming growth factor beta , transforming growth factor , cell , actin , in vitro , genetics , gene
Vascular smooth muscle cell (SMC) differentiation is an essential component of vascular repair and tissue engineering. However, currently used cell models for the study of SMC differentiation have several limitations. Multi-lineage progenitor cells (MLPCs) originate from human umbilical cord blood and are cloned from a single cell. The object of this study was to investigate whether MLPCs could differentiate into SMCs in vitro with induction by transforming growth factor beta1 (TGF-beta1).

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