Literature DB >> 26385570

Correlation of Versican Expression, Accumulation, and Degradation during Embryonic Development by Quantitative Immunohistochemistry.

Jessica M Snyder1, Ida M Washington1, Timothy Birkland2, Mary Y Chang1,2, Charles W Frevert1,2.   

Abstract

Versican, a chondroitin sulfate proteoglycan, is important in embryonic development, and disruption of the versican gene is embryonically lethal in the mouse. Although several studies show that versican is increased in various organs during development, a focused quantitative study on versican expression and distribution during lung and central nervous system development in the mouse has not previously been performed. We tracked changes in versican (Vcan) gene expression and in the accumulation and degradation of versican. Vcan expression and quantitative immunohistochemistry performed from embryonic day (E) 11.5 to E15.5 showed peak Vcan expression at E13.5 in the lungs and brain. Quantitative mRNA analysis and versican immunohistochemistry showed differences in the expression of the versican isoforms in the embryonic lung and head. The expression of Vcan mRNA and accumulation of versican in tissues was complementary. Immunohistochemistry demonstrated co-localization of versican accumulation and degradation, suggesting distinct roles of versican deposition and degradation in embryogenesis. Very little versican mRNA or protein was found in the lungs of 12- to 16-week-old mice but versican accumulation was significantly increased in mice with Pseudomonas aeruginosa lung infection. These data suggest that versican plays an important role in fundamental, overlapping cellular processes in lung development and infection.
© The Author(s) 2015.

Entities:  

Keywords:  DPEAAE; Embryonic development; Pseudomonas aeruginosa; brain; image analysis; immunohistochemistry; lungs; versican

Mesh:

Substances:

Year:  2015        PMID: 26385570      PMCID: PMC4823801          DOI: 10.1369/0022155415610383

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  65 in total

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Authors:  Susanna Popp; Julie S Andersen; Patrice Maurel; Richard U Margolis
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Authors:  Heather Stanton; James Melrose; Christopher B Little; Amanda J Fosang
Journal:  Biochim Biophys Acta       Date:  2011-09-02

Review 4.  Versican and the regulation of cell phenotype in disease.

Authors:  Thomas N Wight; Michael G Kinsella; Stephen P Evanko; Susan Potter-Perigo; Mervyn J Merrilees
Journal:  Biochim Biophys Acta       Date:  2014-01-05

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Authors:  Richard D Kenagy; Anna H Plaas; Thomas N Wight
Journal:  Trends Cardiovasc Med       Date:  2006-08       Impact factor: 6.677

6.  Expression of PG-M(V3), an alternatively spliced form of PG-M without a chondroitin sulfate attachment in region in mouse and human tissues.

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8.  White matter extracellular matrix chondroitin sulfate/dermatan sulfate proteoglycans in multiple sclerosis.

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Journal:  J Neuropathol Exp Neurol       Date:  2001-12       Impact factor: 3.685

9.  Gli2 influences proliferation in the developing lung through regulation of cyclin expression.

Authors:  Martin Rutter; Jinxia Wang; Zhen Huang; Maciej Kuliszewski; Martin Post
Journal:  Am J Respir Cell Mol Biol       Date:  2009-07-02       Impact factor: 6.914

10.  Expression pattern and mapping of the murine versican gene (Cspg2) to chromosome 13.

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Journal:  Genomics       Date:  1995-09-01       Impact factor: 5.736

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  17 in total

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6.  GORAB promotes embryonic lung maturation through antagonizing AKT phosphorylation, versican expression, and mesenchymal cell migration.

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Review 8.  The Use of Quantitative Digital Pathology to Measure Proteoglycan and Glycosaminoglycan Expression and Accumulation in Healthy and Diseased Tissues.

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10.  Versican is produced by Trif- and type I interferon-dependent signaling in macrophages and contributes to fine control of innate immunity in lungs.

Authors:  Mary Y Chang; Inkyung Kang; Michael Gale; Anne M Manicone; Michael G Kinsella; Kathleen R Braun; Tara Wigmosta; William C Parks; William A Altemeier; Thomas N Wight; Charles W Frevert
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