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Publication : Cyp1b1-deficient retinal astrocytes are more proliferative and migratory and are protected from oxidative stress and inflammation.

First Author  Falero-Perez J Year  2019
Journal  Am J Physiol Cell Physiol Volume  316
Issue  6 Pages  C767-C781
PubMed ID  30892936 Mgi Jnum  J:276218
Mgi Id  MGI:6306216 Doi  10.1152/ajpcell.00021.2019
Citation  Falero-Perez J, et al. (2019) Cyp1b1-deficient retinal astrocytes are more proliferative and migratory and are protected from oxidative stress and inflammation. Am J Physiol Cell Physiol 316(6):C767-C781
abstractText  Astrocytes (ACs) are the most abundant cells in the central nervous system. Retinal ACs play an important role in maintaining the integrity of retinal neurovascular function, and their dysfunction contributes to the pathogenesis of various eye diseases including diabetic retinopathy. Cytochrome P450 1B1 (CYP1B1) expression in the neurovascular structures of the central nervous system including ACs has been reported. We previously showed that CYP1B1 expression is a key regulator of redox homeostasis in retinal vascular cells. Its deficiency in mice resulted in increased oxidative stress and attenuation of angiogenesis in vivo and proangiogenic activity of retinal vascular cells in vitro. Here, using retinal ACs prepared from wild-type (Cyp1b1(+/+)) and Cyp1b1-deficient (Cyp1b1(-/-)) mice, we determined the impact of Cyp1b1 expression on retinal AC function. We showed that Cyp1b1(-/-) retinal ACs were more proliferative and migratory. These cells also produced increased amounts of fibronectin and its receptors, alphavbeta3- and alpha5beta1-integrin. These results were consistent with the increased adhesive properties of Cyp1b1(-/-) ACs and their lack of ability to form a network in Matrigel. This was reversed by reexpression of Cyp1b1 in Cyp1b1(-/-) ACs. Although no significant changes were observed in Akt/SRC/MAPK signaling pathways, production of inflammatory mediators bone morphogenetic protein-7 (BMP-7) and monocyte chemoattractant protein-1 (MCP-1) was decreased in Cyp1b1(-/-) ACs. Cyp1b1(-/-) ACs also showed increased levels of connexin 43 phosphorylation and cluster of differentiation 38 expression when challenged with H2O2. These results are consistent with increased proliferation and diminished oxidative stress in Cyp1b1(-/-) cells. Thus, Cyp1b1 expression in ACs plays an important role in retinal neurovascular homeostasis.
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