Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
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Enzyme
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Query: UNIPROT:P01189 (
beta-endorphin
)
21,003
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Group X secretory phospholipase A2
(
GX sPLA2
) hydrolyzes mammalian cell membranes, liberating free fatty acids and lysophospholipids.
GX sPLA2
is produced as a pro-enzyme (pro-
GX sPLA2
) that contains an N-terminal 11-amino acid propeptide ending in a dibasic motif, suggesting cleavage by a furin-like proprotein convertase (PC). Although propeptide cleavage is clearly required for enzymatic activity, the protease(s) responsible for pro-
GX sPLA2
activation have not been identified. We previously reported that
GX sPLA2
negatively regulates adrenal glucocorticoid production, likely by suppressing liver X receptor-mediated activation of steroidogenic acute regulatory protein expression. In this study, using a FLAG epitope-tagged pro-
GX sPLA2
expression construct (FLAG-pro-
GX sPLA2
), we determined that
adrenocorticotropic hormone (ACTH)
enhanced FLAG-pro-
GX sPLA2
processing and phospholipase activity secreted by Y1 adrenal cells. ACTH increased the expression of furin and PCSK6, but not other members of the PC family, in Y1 cells. Overexpression of furin and PCSK6 in HEK 293 cells significantly enhanced FLAG-pro-
GX sPLA2
processing, whereas siRNA-mediated knockdown of both PCs almost completely abolished FLAG-pro-
GX sPLA2
processing in Y1 cells. Expression of either furin or PCSK6 enhanced the ability of
GX sPLA2
to suppress liver X receptor reporter activity. The PC inhibitor decanoyl-Arg-Val-Lys-Arg-chloromethyl ketone significantly suppressed FLAG-pro-
GX sPLA2
processing and sPLA2 activity in Y1 cells, and it significantly attenuated
GX sPLA2
-dependent inhibition of steroidogenic acute regulatory protein expression and progesterone production. These findings provide strong evidence that pro-
GX sPLA2
is a substrate for furin and PCSK6 proteolytic processing and define a novel mechanism for regulating corticosteroid production in adrenal cells.
...
PMID:Ectopically expressed pro-group X secretory phospholipase A2 is proteolytically activated in mouse adrenal cells by furin-like proprotein convertases: implications for the regulation of adrenal steroidogenesis. 2562 68