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Article

Molecular trafficking mechanisms of multipotent mesenchymal stem cells derived from human bone marrow and placenta.

Stem cells and development - 1 Oct 2008

Brooke Gary, Tong Hui, Levesque Jean-Pierre, Atkinson Kerry

Abstract excerpt

We compared potential trafficking mechanisms used by human (h) multipotent mesenchymal stem cells (MSC) derived from bone marrow (bm) or placenta (p). Both hbmMSC and hpMSC expressed a broad range of cell surface adhesion molecules including beta1-integrins (CD29) and CD44. Array data showed that both hbmMSC and hpMSC expressed mRNA for the cell adhesion molecules CD54 (ICAM-1), E-cadherin, CD166 (ALCAM), CD56...

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Source

Identifiers

PMID: 18564033
DOI: 10.1089/scd.2007.0156

Genes

MSC
CXCR4
CXCR6
CCR1
CCR3
ALCAM
CCR10
CCR7
CCR8
CXCL12
CXCR3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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