Literature DB >> 7629154

Hsp47 and cyclophilin B traverse the endoplasmic reticulum with procollagen into pre-Golgi intermediate vesicles. A role for Hsp47 and cyclophilin B in the export of procollagen from the endoplasmic reticulum.

T Smith1, L R Ferreira, C Hebert, K Norris, J J Sauk.   

Abstract

Hsp47 and cyclophilin B (CyPB) are residents of the endoplasmic reticulum (ER). Both of these proteins are closely associated with polysome-associated alpha 1(I) procollagen chains. Hsp47 possesses chaperone properties early during the translation of procollagen while the cis/trans-isomerase properties of CyPB facilitate procollagen folding. In this report, we further investigate the interaction of these proteins with procollagen I during export from the ER. To inhibit vesicular budding and retain procollagen within the ER, cells were treated with the heterotrimeric G protein inhibitor mastoparan or calphostin C, a specific inhibitor of diacylglycerol/phorbol ester binding proteins. To arrest procollagen in pre-Golgi intermediate vesicles, cells were treated with guanosine 5'-3-O-(thio)triphosphate. Pulse-chase experiments of cells labeled with [35S]methionine followed by immunoprecipitation during the chase period with anti-procollagen, anti-Hsp47, and anti-CyPB antibodies were performed to reveal the relationship between Hsp47/CyPB/procollagen I. The distribution of procollagen, Hsp47, and CyPB to the ER and/or pre-Golgi vesicles was verified by immunofluorescence. Hsp47 and CyPB remained associated with procollagen retained within the ER. Hsp47 and CyPB were also associated with procollagen exported from the ER into pre-Golgi intermediate vesicles. Treatment of cells with cyclosporin A diminished the levels of CyPB bound to procollagen and diminished the rate of Hsp47 released from procollagen and the rate of procollagen secretion, suggesting that Hsp47 release from procollagen may be driven by helix formation. Also, these studies suggest that Hsp47 may resemble protein disulfide isomerase and possess both chaperone and anti-chaperone properties. During translation, high levels of Hsp47 are seen to limit protein aggregation and facilitate chain registration. Later, Hsp47 and/or CyPB and protein disulfide isomerase act as anti-chaperones and provide the basis for concentration of procollagen for ER export.

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Year:  1995        PMID: 7629154     DOI: 10.1074/jbc.270.31.18323

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  33 in total

1.  Mapping Hsp47 binding site(s) using CNBr peptides derived from type I and type II collagen.

Authors:  Christy A Thomson; Ruggero Tenni; Vettai S Ananthanarayanan
Journal:  Protein Sci       Date:  2003-08       Impact factor: 6.725

2.  Cloning and biochemical characterization of the cyclophilin homologues from the free-living nematode Caenorhabditis elegans.

Authors:  A P Page; K MacNiven; M O Hengartner
Journal:  Biochem J       Date:  1996-07-01       Impact factor: 3.857

Review 3.  Chaperoning osteogenesis: new protein-folding disease paradigms.

Authors:  Elena Makareeva; Nydea A Aviles; Sergey Leikin
Journal:  Trends Cell Biol       Date:  2010-12-21       Impact factor: 20.808

4.  Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta.

Authors:  Uschi Lindert; Mary Ann Weis; Jyoti Rai; Frank Seeliger; Ingrid Hausser; Tosso Leeb; David Eyre; Marianne Rohrbach; Cecilia Giunta
Journal:  J Biol Chem       Date:  2015-05-24       Impact factor: 5.157

Review 5.  New perspectives on osteogenesis imperfecta.

Authors:  Antonella Forlino; Wayne A Cabral; Aileen M Barnes; Joan C Marini
Journal:  Nat Rev Endocrinol       Date:  2011-06-14       Impact factor: 43.330

6.  A substrate preference for the rough endoplasmic reticulum resident protein FKBP22 during collagen biosynthesis.

Authors:  Yoshihiro Ishikawa; Hans Peter Bächinger
Journal:  J Biol Chem       Date:  2014-05-12       Impact factor: 5.157

7.  An additional function of the rough endoplasmic reticulum protein complex prolyl 3-hydroxylase 1·cartilage-associated protein·cyclophilin B: the CXXXC motif reveals disulfide isomerase activity in vitro.

Authors:  Yoshihiro Ishikawa; Hans Peter Bächinger
Journal:  J Biol Chem       Date:  2013-09-16       Impact factor: 5.157

8.  Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding.

Authors:  Aileen M Barnes; Erin M Carter; Wayne A Cabral; MaryAnn Weis; Weizhong Chang; Elena Makareeva; Sergey Leikin; Charles N Rotimi; David R Eyre; Cathleen L Raggio; Joan C Marini
Journal:  N Engl J Med       Date:  2010-01-20       Impact factor: 91.245

9.  Severe osteogenesis imperfecta in cyclophilin B-deficient mice.

Authors:  Jae Won Choi; Shari L Sutor; Lonn Lindquist; Glenda L Evans; Benjamin J Madden; H Robert Bergen; Theresa E Hefferan; Michael J Yaszemski; Richard J Bram
Journal:  PLoS Genet       Date:  2009-12-04       Impact factor: 5.917

10.  PPIB mutations cause severe osteogenesis imperfecta.

Authors:  Fleur S van Dijk; Isabel M Nesbitt; Eline H Zwikstra; Peter G J Nikkels; Sander R Piersma; Silvina A Fratantoni; Connie R Jimenez; Margriet Huizer; Alice C Morsman; Jan M Cobben; Mirjam H H van Roij; Mariet W Elting; Jonathan I M L Verbeke; Liliane C D Wijnaendts; Nick J Shaw; Wolfgang Högler; Carole McKeown; Erik A Sistermans; Ann Dalton; Hanne Meijers-Heijboer; Gerard Pals
Journal:  Am J Hum Genet       Date:  2009-09-24       Impact factor: 11.025

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