Comprehensive Screening of Cell Surface Markers Expressed by Adult-Derived Human Liver Stem/Progenitor Cells Harvested at Passage 5: Potential Implications for Engraftment.

Stem Cells Int

Laboratory of Pediatric Hepatology and Cell Therapy, Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain, Avenue Mounier 52, 1200 Bruxelles, Belgium.

Published: November 2016

AI Article Synopsis

  • MSCs might offer therapeutic benefits, but studies show they typically have low engraftment in target organs due to lacking important receptors.
  • ADHLSCs, a type of liver stem cell, do not express many costimulatory molecules and lack key adhesion molecules crucial for effective engraftment.
  • The research indicates that the ability to bind to endothelial cells could be the main hurdle preventing successful engraftment of MSCs in damaged organs.

Article Abstract

Mesenchymal stromal cells (MSCs) are known to have potential therapeutic benefits for a number of diseases. However, many studies report low engraftment levels, regardless of the target organ. One possible explanation could be that MSCs do not express the necessary receptors for engraftment. Indeed, MSCs appear to use a similar mechanism to leukocytes to engraft into injured organs, relying on various receptors for rolling, firm adhesion, and transmigration. In this study, we conducted an extensive surface molecule screening of adult-derived human liver stem/progenitor cells (ADHLSC) in an attempt to shed some light on this subject. We observed that ADHLSCs lack expression of most of the costimulatory molecules tested. Furthermore, study of the adhesion molecule profile of ADHLSCs revealed that they do not express selectin ligands or LFA-1 which are, respectively, involved in the rolling process and the firm adhesion. In addition, ADHLSCs slightly express VLA-4 and lose expression of CXCR4 altogether on their surface during culture expansion. However, ADHLSCs express all the integrin couples and matrix metalloproteinases needed to bind and integrate the extracellular matrix once the endothelial barrier is crossed. Collectively, these results suggest that binding to the endothelium may be the critical weak point in the engraftment process.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124472PMC
http://dx.doi.org/10.1155/2016/9302537DOI Listing

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