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Cited by 2,381

The DOI matches its Crossref record; 121 of the 121 references it cites were found in a registry or an index.

Concise Review: Mesenchymal Stem Cells: Their Phenotype, Differentiation Capacity, Immunological Features, and Potential for Homing

Chamberlain, Giselle, Fox, James, Ashton, Brian, Middleton, Jim·2007·Stem Cells

Abstract

MSCs are nonhematopoietic stromal cells that are capable of differentiating into, and contribute to the regeneration of, mesenchymal tissues such as bone, cartilage, muscle, ligament, tendon, and adipose. MSCs are rare in bone marrow, representing ∼1 in 10,000 nucleated cells. Although not immortal, they have the ability to expand manyfold in culture while retaining their growth and multilineage potential. MSCs are identified by the expression of many molecules including CD105 (SH2) and CD73 (SH3/4) and are negative for the hematopoietic markers CD34, CD45, and CD14. The properties of MSCs make these cells potentially ideal candidates for tissue engineering. It has been shown that MSCs, when transplanted systemically, are able to migrate to sites of injury in animals, suggesting that MSCs possess migratory capacity. However, the mechanisms underlying the migration of these cells remain unclear. Chemokine receptors and their ligands and adhesion molecules play an important role in tissue-specific homing of leukocytes and have also been implicated in trafficking of hematopoietic precursors into and through tissue. Several studies have reported the functional expression of various chemokine receptors and adhesion molecules on human MSCs. Harnessing the migratory potential of MSCs by modulating their chemokine-chemokine receptor interactions may be a powerful way to increase their ability to correct inherited disorders of mesenchymal tissues or facilitate tissue repair in vivo. The current review describes what is known about MSCs and their capacity to home to tissues together with the associated molecular mechanisms involving chemokine receptors and adhesion molecules. Disclosure of potential conflicts of interest is found at the end of this article.

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Crossref · 10.1634/stemcells.2007-0197

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Metadata

Authors
Chamberlain, G., Fox, J., Ashton, B., & Middleton, J.
Venue
Stem Cells
Published
2007-07-26
Volume
25
Issue
11
Pages
2739-2749
ISSN
  • 1066-5099 (ISSN-L)
  • 1549-4918
OpenAlex
W1965425745
Cited by
2,381
References
121
FWCI
43.44
Type
journal article
Language
en
Open access
closed

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