Human bone marrow-derived mesenchymal stem cells differentiate into epidermal-like cells in vitro.

Differentiation

The Second Affiliated Hospital of Medicine College, Zhejiang University, Hangzhou, China.

Published: April 2007

AI Article Synopsis

  • - The study focuses on the potential of human bone marrow-derived mesenchymal stem cells (hMSCs) to differentiate into epidermal-like cells in vitro under specific conditions.
  • - Researchers found that when exposed to an inducing medium, hMSCs expressed key markers associated with epidermal cells and changed their morphology, indicating successful differentiation.
  • - The findings suggest that hMSCs have multipotential capabilities, opening new avenues for research into their applications in skin-related therapies and regenerative medicine.

Article Abstract

Human bone marrow-derived mesenchymal stem cells (hMSCs) are a population of pluripotent cells. They can differentiate into different embryonic layer cells as osteoblasts, adipocytes, chondrocytes, myoblasts, neurocytes, etc. However, there are only few reports with regard to differentiate hMSCs into epidermal cells in vitro. In this study, we want to investigate the feasibility of inducing hMSCs into epidermal-like cells under specific medium in vitro. hMSCs in specific inducing medium expressed the early markers of epidermal cell lineage, P63, cytokeratin19 (CK19), the late differentiated marker, the pan-cytokeratin, and another early marker, the beta1-integrin, which up-regulated remarkably in inducing medium. Their morphologies were changed from spindle-like fibroblastic appearances to oblate or irregular shapes under phase contrast microscopy. The hemidesmosome structure was found using the transmission electron microscope. All these data suggested that, under certain conditions, hMSCs have the potential to differentiate into epidermal-like cells. It will be of great accordance in the study of the multipotential property of hMSCs.

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Source
http://dx.doi.org/10.1111/j.1432-0436.2006.00140.xDOI Listing

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