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  • Batool, TahiraUppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Science for Life Laboratory, SciLifeLab (author)

Upregulated BMP-Smad signaling activity in the glucuronyl C5-epimerase knock out MEF cells

  • Article/chapterEnglish2019

Publisher, publication year, extent ...

  • Elsevier,2019
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:uu-363254
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-363254URI
  • https://doi.org/10.1016/j.cellsig.2018.11.010DOI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Glucuronyl C5-epimerase (Hsepi) catalyzes the conversion of glucuronic acid to iduronic acid in the process of heparan sulfate biosynthesis. Targeted interruption of the gene, Glce,in mice resulted in neonatal lethality with varied defects in organ development. To understand the molecular mechanisms of the phenotypes, we used mouse embryonic fibroblasts (MEF) as a model to examine selected signaling pathways. Our earlier studies found reduced activities of FGF-2, GDNF, but increased activity of sonic hedgehog in the mutant cells. In this study, we focused on the bone morphogenetic protein (BMP) signaling pathway. Western blotting detected substantially elevated endogenous Smad1/5/8 phosphorylation in the Hsepi mutant (KO) MEF cells, which is reverted by re-expression of the enzyme in the KO cells. The mutant cells displayed an enhanced proliferation and elevated alkaline phosphatase activity, marking higher differentiation, when cultured in osteogenic medium. The high level of Smad1/5/8 phosphorylation was also found in primary calvarial cells isolated from the KO mice. Analysis of the genes involved in the BMP signaling pathway revealed upregulation of a number of BMP ligands, but reduced expression of several Smads and BMP antagonist (Grem1) in the KO MEF cells. The results suggest that Hsepi expression modulates BMP signaling activity, which, at least partially, is associated with defected molecular structure of heparan sulfate expressed in the cells.   

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Added entries (persons, corporate bodies, meetings, titles ...)

  • Fang, JianpingUppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Glyconovo Technologies Co., Ltd., TianXiong Road, Shanghai International Medical Zone (SIMZ), Pudong New Area, Shanghai 201318, China(Swepub:uu)jiafa429 (author)
  • Jansson, ViktorUppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi (author)
  • Zhao, HongxingUppsala universitet,Science for Life Laboratory, SciLifeLab(Swepub:uu)hongzhao (author)
  • Gallant, Caroline J.Uppsala universitet,Science for Life Laboratory, SciLifeLab(Swepub:uu)carga920 (author)
  • Moustakas, AristidisUppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Science for Life Laboratory, SciLifeLab(Swepub:uu)arimo287 (author)
  • Li, Jin-PingUppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Science for Life Laboratory, SciLifeLab(Swepub:uu)jinpili (author)
  • Uppsala universitetInstitutionen för medicinsk biokemi och mikrobiologi (creator_code:org_t)

Related titles

  • In:Cellular Signalling: Elsevier54, s. 122-1290898-65681873-3913

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