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

Authors :
UCL - SSS/IREC/PEDI - Pôle de Pédiatrie
UCL - (SLuc) Service de gastro-entérologie et hépatologie pédiatrique
Dollet, Pierre-Edouard
Ravau, Joachim
André, Floriane
Najimi, Mustapha
Sokal, Etienne
Lombard, Catherine
UCL - SSS/IREC/PEDI - Pôle de Pédiatrie
UCL - (SLuc) Service de gastro-entérologie et hépatologie pédiatrique
Dollet, Pierre-Edouard
Ravau, Joachim
André, Floriane
Najimi, Mustapha
Sokal, Etienne
Lombard, Catherine
Source :
Stem Cells International, Vol. 2016, p. 9302537 [1-12] (2016)
Publication Year :
2016

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.

Details

Database :
OAIster
Journal :
Stem Cells International, Vol. 2016, p. 9302537 [1-12] (2016)
Notes :
Ndonga
Publication Type :
Electronic Resource
Accession number :
edsoai.on1130465780
Document Type :
Electronic Resource