Linked Life Data

20555025

Source:http://linkedlifedata.com/resource/pubmed/id/20555025

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2010-7-27
pubmed:abstractText
Bone morphogenetic proteins (BMPs) require major posttranslational modifications to become biologically active. One such key modification is endoproteolytic cleavage of the initially synthesized nonactive precursor protein to release the mature ligand. Here we show in a physiological context of uterine stromal decidualization that BMP2 cleavage is mediated by proprotein convertase 5/6 (PC6). Decidualization is a uterine remodeling event critical for embryo implantation. Deletion or knockdown of either BMP2 or PC6 inhibits decidualization causing implantation failure and female infertility. In this study we provide biochemical and physiological evidence that PC6 proteolytically activates BMP2. We used freshly isolated primary human endometrial stromal cells and demonstrated that PC6 was the sole member of the PC family significantly up-regulated during decidualization. The precursor form of BMP2 was reduced, whereas its active form was increased during decidualization. Inhibition of PC6 activity inhibited decidualization, and this was accompanied by a total blockade of BMP2 activation. Addition of recombinant active BMP2 partially rescued the decidualization arrest caused by PC6 inhibition. PC6 processed BMP2 at the KREKR(282) downward arrow cleavage site, and mutating this site prevented the cleavage. This study thus demonstrates for the first time that the proteolytic activation and thus bioavailability of BMP2 is controlled by PC6.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1945-7170
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
151
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3909-17
pubmed:meshHeading
pubmed-meshheading:20555025-Amino Acid Sequence, pubmed-meshheading:20555025-Bone Morphogenetic Protein 2, pubmed-meshheading:20555025-Catalytic Domain, pubmed-meshheading:20555025-Cells, Cultured, pubmed-meshheading:20555025-Dose-Response Relationship, Drug, pubmed-meshheading:20555025-Embryo Implantation, pubmed-meshheading:20555025-Endometrium, pubmed-meshheading:20555025-Enzyme Inhibitors, pubmed-meshheading:20555025-Female, pubmed-meshheading:20555025-Fluoresceins, pubmed-meshheading:20555025-Humans, pubmed-meshheading:20555025-Pregnancy, pubmed-meshheading:20555025-Pregnancy Maintenance, pubmed-meshheading:20555025-Proprotein Convertase 5, pubmed-meshheading:20555025-Protein Processing, Post-Translational, pubmed-meshheading:20555025-Up-Regulation, pubmed-meshheading:20555025-Validation Studies as Topic
pubmed:year
2010
pubmed:articleTitle
Posttranslational activation of bone morphogenetic protein 2 is mediated by proprotein convertase 6 during decidualization for pregnancy establishment.
pubmed:affiliation
Prince Henry's Institute of Medical Research, Clayton, Victoria 3168, Australia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't