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Publication : Sfrp1 deficiency makes retinal photoreceptors prone to degeneration.

First Author  Cisneros E Year  2020
Journal  Sci Rep Volume  10
Issue  1 Pages  5115
PubMed ID  32198470 Mgi Jnum  J:286686
Mgi Id  MGI:6405078 Doi  10.1038/s41598-020-61970-8
Citation  Cisneros E, et al. (2020) Sfrp1 deficiency makes retinal photoreceptors prone to degeneration. Sci Rep 10(1):5115
abstractText  Millions of individuals worldwide suffer from impaired vision, a condition with multiple origins that often impinge upon the light sensing cells of the retina, the photoreceptors, affecting their integrity. The molecular components contributing to this integrity are however not yet fully understood. Here we have asked whether Secreted Frizzled Related Protein 1 (SFRP1) may be one of such factors. SFRP1 has a context-dependent function as modulator of Wnt signalling or of the proteolytic activity of A Disintegrin And Metalloproteases (ADAM) 10, a main regulator of neural cell-cell communication. We report that in Sfrp1(-/-) mice, the outer limiting membrane (OLM) is discontinuous and the photoreceptors disorganized and more prone to light-induced damage. Sfrp1 loss significantly enhances the effect of the Rpe65(Leu450Leu) genetic variant -present in the mouse genetic background- which confers sensitivity to light-induced stress. These alterations worsen with age, affect visual function and are associated to an increased proteolysis of Protocadherin 21 (PCDH21), localized at the photoreceptor outer segment, and N-cadherin, an OLM component. We thus propose that SFRP1 contributes to photoreceptor fitness with a mechanism that involves the maintenance of OLM integrity. These conclusions are discussed in view of the broader implication of SFRP1 in neurodegeneration and aging.
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