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FGF signals induce Caprin2 expression in the vertebrate lens.
Umeå universitet, Medicinska fakulteten, Umeå centrum för molekylär medicin (UCMM).
Umeå universitet, Medicinska fakulteten, Umeå centrum för molekylär medicin (UCMM).ORCID-id: 0000-0001-5923-8572
Umeå universitet, Medicinska fakulteten, Umeå centrum för molekylär medicin (UCMM).
2009 (engelsk)Inngår i: Differentiation, ISSN 0301-4681, E-ISSN 1432-0436, Vol. 77, nr 4, s. 386-394Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The lens of the eye is derived from the non-neural ectoderm situated next to the optic vesicle. Fibroblast growth factor (FGF) signals play a major role at various stages of vertebrate lens development ranging from induction and proliferation to differentiation. Less is however known about the identity of genes that are induced by FGF activity within the lens. We have isolated and characterized mouse cytoplasmic activation/proliferation-associated protein-2 (Caprin2), with domains belonging to both the Caprin family and the C1q and tumour necrosis factor (TNF) super-family. Here we show that Caprin2 is expressed in the developing vertebrate lens in mouse and chick, and that Caprin2 expression is up-regulated in primary lens fiber cells, after the induction of crystallins the earliest known markers for differentiated lens fiber cells. Caprin2 is subsequently down-regulated in the centre of the lens at the time and at the position of the first fiber cell denucleation and terminal differentiation. In vitro analyses of lens fiber cell differentiation provide evidence that FGF activity emanating from neighboring prospective retinal cells is required and that FGF8 activity is sufficient to induce Caprin2 in lens fiber cells. These results not only provide evidence that FGF signals induce the newly characterized protein Caprin2 in the lens, but also support the general idea that FGF signals are required for lens fiber cell differentiation.

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2009. Vol. 77, nr 4, s. 386-394
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URN: urn:nbn:se:umu:diva-31455DOI: 10.1016/j.diff.2008.11.003PubMedID: 19275872Scopus ID: 2-s2.0-61649103575OAI: oai:DiVA.org:umu-31455DiVA, id: diva2:293096
Tilgjengelig fra: 2010-02-10 Laget: 2010-02-10 Sist oppdatert: 2023-03-23bibliografisk kontrollert

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