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Publication : Smad3 is necessary for transforming growth factor-beta2 induced ocular hypertension in mice.

First Author  McDowell CM Year  2013
Journal  Exp Eye Res Volume  116
Pages  419-23 PubMed ID  24184030
Mgi Jnum  J:210389 Mgi Id  MGI:5570993
Doi  10.1016/j.exer.2013.10.017 Citation  McDowell CM, et al. (2013) Smad3 is necessary for transforming growth factor-beta2 induced ocular hypertension in mice. Exp Eye Res 116:419-23
abstractText  TGFbeta2 induces extracellular matrix (ECM) remodeling and alters the cytoskeleton by both the canonical Smad and non-canonical signaling pathways. TGFbeta2 regulates the expression of ECM proteins in trabecular meshwork (TM) cells, increases intraocular pressure (IOP) in an ex vivo perfusion organ culture model, and induces ocular hypertension in rodent eyes. A necessary step in the canonical Smad signaling pathway is phosphorylation of receptor protein Smad3 by the TGF-beta receptor complex. The purpose of this study was to determine whether TGFbeta2 signals in vivo through the canonical Smad signaling pathway in the TM using Smad3 knockout (KO) mice. Ad5.hTGFbeta2(226/228) (2.5 x 10(7) pfu) was injected intravitreally into one eye of homozygous (WT), heterozygous (HET), and homozygous (KO) 129-Smad3(tm1Par)/J mice (n = 9-10 mice/group), with the uninjected contralateral eye serving as the control. IOP measurements were taken using a rebound tonometer. To test the effect of TGFbeta2 signaling on the ECM, fibronectin expression was determined by immunohistochemistry and qPCR analysis. Transduction of the TM with viral vector Ad5.hTGFbeta2(226/228) caused a statistically significant difference in IOP exposure between Smad3 genotypes: WT, 187.7 +/- 23.9 mmHg*day (n = 9); HET, 95.6 +/- 24.5 mmHg*day (n = 9); KO, 52.8 +/- 25.2 mmHg*day (n = 10); (p < 0.05 WT versus HET, p < 0.01 WT versus KO). Immunohistochemistry and qPCR analysis showed that Ad5.hTGFbeta2(226/228) increased fibronectin expression in the TM of WT mice (2.23 +/- 0.24 fold) compared to Smad3 KO mice (0.99 +/- 0.19 fold), p < 0.05. These results demonstrate Smad3 is a necessary signaling protein for TGFbeta2-induced ocular hypertension and fibronectin deposition in the TM.
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