Literature DB >> 17122142

CTRP5 is a membrane-associated and secretory protein in the RPE and ciliary body and the S163R mutation of CTRP5 impairs its secretion.

Md Nawajes A Mandal1, Vidyullatha Vasireddy, G Bhanuprakash Reddy, Xiaofei Wang, Sayoko E Moroi, Bikash R Pattnaik, Bret A Hughes, John R Heckenlively, Peter F Hitchcock, Monica M Jablonski, Radha Ayyagari.   

Abstract

PURPOSE: In a prior study, a S163R mutation in the complement-1q tumor necrosis factor-related protein 5 (CTRP5/ C1QTNF5) was reported to be associated with early-onset long anterior zonules (LAZ) and late-onset retinal degeneration (L-ORD). The ocular tissues involved in the phenotype are the retinal pigment epithelium (RPE) in the posterior segment and ciliary epithelium (CE) and lens in the anterior segment. The purpose of this study was to characterize the spatial and temporal expression of the mouse Ctrp5 gene, determine tissue and subcellular localization, and study the effect of the S163R mutation.
METHODS: The expression of the Ctrp5 gene in the mouse was studied by quantitative (q)RT-PCR and in situ hybridization. CTRP5 protein expression and distribution were studied by Western blot analysis, immunohistochemistry, and immunoelectron microscopy. Cellular location of wild-type and mutant CTRP5 in MDCK and COS-7 cells was determined by immunofluorescence and immunoblot analysis.
RESULTS: A significant level of Ctrp5 expression was detected in the adult mouse in the ciliary body (CB) and RPE, and expression started at a very early stage of embryogenesis. Immunohistochemical analysis showed CTRP5 protein in the apical processes of the RPE and forming a hexagonal lattice associated with the RPE lateral membranes. In the ciliary body, CTRP5 was localized to the apical aspects of the CE, the region between the bilayered ciliary epithelial cells. The membrane association of CTRP5 in the RPE and CE was further confirmed by immunoelectron microscopy. Furthermore, cultured cells were used to show that the CTRP5 is a secretory protein and that its secretion is impaired by the S163R mutation.
CONCLUSIONS: CTRP5, a secretory and membrane-associated protein, is localized to the lateral and apical membranes of the RPE and CB. Impaired secretion of the mutant protein may underlie the pathophysiology of L-ORD and LAZ.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 17122142     DOI: 10.1167/iovs.06-0312

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  42 in total

1.  C1q/TNF-related proteins, a family of novel adipokines, induce vascular relaxation through the adiponectin receptor-1/AMPK/eNOS/nitric oxide signaling pathway.

Authors:  Qijun Zheng; Yuexing Yuan; Wei Yi; Wayne Bond Lau; Yajing Wang; Xiaoliang Wang; Yang Sun; Bernard L Lopez; Theodore A Christopher; Jonathan M Peterson; G William Wong; Shiqiang Yu; Dinghua Yi; Xin-Liang Ma
Journal:  Arterioscler Thromb Vasc Biol       Date:  2011-11       Impact factor: 8.311

2.  Retinol dehydrogenases RDH11 and RDH12 in the mouse retina: expression levels during development and regulation by oxidative stress.

Authors:  Yogita Kanan; Lea D Wicker; Muayyad R Al-Ubaidi; Nawajes A Mandal; Anne Kasus-Jacobi
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-03       Impact factor: 4.799

3.  Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene.

Authors:  Bo Chang; Md Nawajes A Mandal; Venkata R M Chavali; Norman L Hawes; Naheed W Khan; Ronald E Hurd; Richard S Smith; Muriel L Davisson; Laura Kopplin; Barbara E K Klein; Ronald Klein; Sudha K Iyengar; John R Heckenlively; Radha Ayyagari
Journal:  Hum Mol Genet       Date:  2008-09-18       Impact factor: 6.150

4.  Pathological Effects of Mutant C1QTNF5 (S163R) Expression in Murine Retinal Pigment Epithelium.

Authors:  Astra Dinculescu; Seok-Hong Min; Frank M Dyka; Wen-Tao Deng; Rachel M Stupay; Vince Chiodo; W Clay Smith; William W Hauswirth
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-10       Impact factor: 4.799

5.  A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration.

Authors:  Venkata R M Chavali; Naheed W Khan; Catherine A Cukras; Dirk-Uwe Bartsch; Monica M Jablonski; Radha Ayyagari
Journal:  Hum Mol Genet       Date:  2011-02-24       Impact factor: 6.150

6.  Long-Term Effects of Gene Therapy in a Novel Mouse Model of Human MFRP-Associated Retinopathy.

Authors:  Anil Chekuri; Bhubanananda Sahu; Venkata Ramana Murthy Chavali; Marina Voronchikhina; Angel Soto-Hermida; John J Suk; Akhila N Alapati; Dirk-Uwe Bartsch; Raul Ayala-Ramirez; Juan C Zenteno; Astra Dinculescu; Monica M Jablonski; Shyamanga Borooah; Radha Ayyagari
Journal:  Hum Gene Ther       Date:  2019-01-16       Impact factor: 5.695

7.  Expression and localization of CERKL in the mammalian retina, its response to light-stress, and relationship with NeuroD1 gene.

Authors:  Nawajes A Mandal; Julie-Thu A Tran; Anisse Saadi; Abul K Rahman; Tuan-Phat Huynh; William H Klein; Jang-Hyeon Cho
Journal:  Exp Eye Res       Date:  2012-11-08       Impact factor: 3.467

8.  Ets-2 is involved in transcriptional regulation of C1qTNF-related protein 5 in muscle cells.

Authors:  Eun-Ju Park; Mi-Jin Kim; Wan Lee; Seung-Yoon Park
Journal:  Mol Biol Rep       Date:  2012-06-28       Impact factor: 2.316

9.  Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments.

Authors:  Jungyeon Won; Richard S Smith; Neal S Peachey; Jiang Wu; Wanda L Hicks; Jürgen K Naggert; Patsy M Nishina
Journal:  Vis Neurosci       Date:  2008 Jul-Aug       Impact factor: 3.241

Review 10.  Metabolic function of the CTRP family of hormones.

Authors:  Marcus M Seldin; Stefanie Y Tan; G William Wong
Journal:  Rev Endocr Metab Disord       Date:  2014-06       Impact factor: 6.514

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.