Abnormal uterus with polycysts, accumulation of uterine prostaglandins, and reduced fertility in mice heterozygous for acyl-CoA synthetase 4 deficiency
Authors
Cho, YY
Kang, MJ
Sone, H
Suzuki, T
Abe, M
Igarashi, M
Tokunaga, T
Ogawa, S
Takei, YA
Miyazawa, T
Sasano, H
Fujino, T
Yamamoto, TT
Citation
Yy. Cho et al., Abnormal uterus with polycysts, accumulation of uterine prostaglandins, and reduced fertility in mice heterozygous for acyl-CoA synthetase 4 deficiency, BIOC BIOP R, 284(4), 2001, pp. 993-997
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
SICI code
0006-291X(20010622)284:4<993:AUWPAO>2.0.ZU;2-U
Abstract
Arachidonate released by various stimuli is rapidly reesterified into membr
ane phospholipids initiated by acyl-CoA synthetase (ACS) and subsequent acy
l-transfer reactions. ACS4 is an arachidonate-preferring enzyme abundant in
steroidogenic tissues and postulated to modulate eicosanoid production. Fe
male mice heterozygous for ACS4 deficiency become pregnant less frequently
and produce small Litters with extremely low transmission of the disrupted
alleles. Striking morphological changes, including extremely enlarged uteri
and lumina filled with numerous proliferative cysts of various sizes, were
detected in ACS4+/- females, Furthermore, marked accumulation of prostagla
ndins was seen in the uterus of the heterozygous females. These results ind
icate that ACS4 modulates female fertility and uterine prostaglandin produc
tion. (C) zool Academic Press.