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Hyaluronan fragments induce endothelial cell differentiation in a CD44- and CXCL1/GRO1-dependent manner
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm , Ludwig Institute for Cancer Research.
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2005 (English)In: J Biol Chem, ISSN 411913200, Vol. 280, no 25, 24195-24204 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2005. Vol. 280, no 25, 24195-24204 p.
URN: urn:nbn:se:uu:diva-94339OAI: oai:DiVA.org:uu-94339DiVA: diva2:168158
Available from: 2006-04-27 Created: 2006-04-27 Last updated: 2011-01-31Bibliographically approved
In thesis
1. Effect of Hyaluronan-activation of CD44 on Cell Signaling and Tumorigenesis
Open this publication in new window or tab >>Effect of Hyaluronan-activation of CD44 on Cell Signaling and Tumorigenesis
2006 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Hyaluronan (HA), a structural component in the extracellular matrix (ECM), has been recognized as a signaling molecule. It is important during various biological activities such as embryogenesis, angiogenesis, wound healing and tumor progression. Increased amount of hyaluronan during embryonic development is necessary for cell migration and differentiation, but the increased production of hyaluronan by tumor cells or tissue fibroblasts is correlated to poor prognosis for tumor progression and chronic inflammation, respectively. Therefore, understanding the mechanisms regulating HA-enriched matrices and the roles of HA in the biological functions is of fundamental biological importance.

Four novel findings are described in this thesis: (1) HA fragments (HA12) and the known angiogenic factor FGF-2 promote endothelial cell differentiation by induction of common but also distinct sets of genes, particularly, upregulation of the chemokine CXCL1/GRO1 gene is necessary for HA12-induced angiogenesis and this effect is dependent on CD44 activation. (2) High concentrations of hyaluronan suppress PDGF-BB-induced fibroblasts migration and PDGFRβ tyrosine phosphorylation upon activation of hyaluronan receptor CD44, probably by recruiting a CD44-associated phosphatase to the PDGFRβ. (3) PDGF-BB stimulates HAS2 transcriptional activity and HA synthesis through upregulation of MAP kinase and PI3 kinase signaling pathways in human dermal fibroblasts. (4) Specific suppression of HAS2 gene in the invasive breast cancer cell line Hs578T by RNA interference (RNAi) leads to a less aggressive phenotype of breast tumor cells. This suppressive effect can be reversed by exogenously added hyaluronan.

In conclusion, binding of hyaluronan to CD44 plays an important role in cell signaling, inflammation and tumor progression. Further studies are required to elucidate the molecular mechanisms through which hyaluronan levels are regulated under physiological or pathological conditions, and to explore compounds involved in hyaluronan accumulation and activity as targets for therapies of chronic inflammation and tumors.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2006. 38 p.
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 1651-6206 ; 142
Biomedicine, Hyaluronan, CD44, growth factors, chemokines, tumorigenesis, wound healing, cell signaling, Biomedicin
urn:nbn:se:uu:diva-6802 (URN)91-554-6537-4 (ISBN)
Public defence
2006-05-22, Room B21, BMC, Uppsala, 13:15
Available from: 2006-04-27 Created: 2006-04-27Bibliographically approved

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