Literature DB >> 1843353

Differential origin and control mechanisms in small and large bovine luteal cells.

W Hansel1, H W Alila, J P Dowd, R A Milvae.   

Abstract

Studies of the calcium requirement and the relationship of intracellular calcium to progesterone synthesis in highly purified preparations of bovine luteal cells reveal a remarkably close relationship between intracellular calcium levels and steroidogenesis. The differential responses of the two cell types, summarized in Table 2, are beginning to reveal how the two cell types may co-operate to produce both luteotrophic and luteolytic responses at different stages of the oestrous cycle and early pregnancy. The luteotrophic mechanisms in the small cells are fairly clear; in addition to the luteotrophic effects of LH and cAMP, activation of protein kinase C leads to increased progesterone synthesis. Accordingly, PGF-2 alpha and several other prostanoids are luteotrophic in these cells. PGF-2 alpha stimulates phospholipase C activity in the small cells but does not reduce LH-stimulated cAMP or progesterone accumulation (Davis et al., 1989). This acute stimulus of protein kinase C activation to progesterone production in bovine small luteal cells is rapidly desensitized, although its stimulus to prostanoid production continues for at least 24 h. Large cells respond to LH, but only at relatively high levels. In addition, we have no good evidence for a role for protein kinase C in the control of progesterone synthesis in the large bovine luteal cells from mid-cycle corpora lutea. Phorbol esters have no effect on steroidogenesis and it is not yet established that protein kinase C provides the same high affinity receptor for phorbol esters that is found in the small cells. Experiments with inhibitors of protein kinase C, such as staurosporine, in large cells have been inconclusive. Evidence for several species suggests that both cell types co-operate, in ways not yet fully understood, to bring about maximal progesterone production at mid-cycle. Some evidence suggests that they may also co-operate to bring about luteolysis. The concept that PGF-2 alpha initiates luteolysis by inhibiting LH stimulated progesterone production in the large cells must be revised in light of the relative insensitivity of these cells to LH and the fact that they probably constitutively express the cholesterol side-chain cleavage enzymes (P-450scc) that represent the rate-limiting step in progesterone production. Oonk et al. (1989) have reported that, once P-450scc mRNA is induced in rat granulosa cells by the LH surge, it is constitutively maintained by the luteinized cells in the absence of gonadotrophins and is no longer regulated by cAMP.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1843353

Source DB:  PubMed          Journal:  J Reprod Fertil Suppl        ISSN: 0449-3087


  12 in total

1.  Luteinizing hormone stimulates mammalian target of rapamycin signaling in bovine luteal cells via pathways independent of AKT and mitogen-activated protein kinase: modulation of glycogen synthase kinase 3 and AMP-activated protein kinase.

Authors:  Xiaoying Hou; Edward W Arvisais; John S Davis
Journal:  Endocrinology       Date:  2010-03-29       Impact factor: 4.736

2.  Effects of luteinizing hormone and prostaglandin F(2α) on gap junctional intercellular communication of ovine luteal cells throughout the estrous cycle.

Authors:  A T Grazul-Bilska; D A Redmer; L P Reynolds
Journal:  Endocrine       Date:  1996-10       Impact factor: 3.633

Review 3.  History, insights, and future perspectives on studies into luteal function in cattle.

Authors:  Cecily V Bishop; Vimal Selvaraj; David H Townson; Joy L Pate; Milo C Wiltbank
Journal:  J Anim Sci       Date:  2022-07-01       Impact factor: 3.338

4.  Luteinizing hormone regulates the phosphorylation and localization of the mitochondrial effector dynamin-related protein-1 (DRP1) and steroidogenesis in the bovine corpus luteum.

Authors:  Michele R Plewes; Xiaoying Hou; Heather A Talbott; Pan Zhang; Jennifer R Wood; Andrea S Cupp; John S Davis
Journal:  FASEB J       Date:  2020-02-20       Impact factor: 5.834

5.  Gene expression profiling of bovine ovarian follicular and luteal cells provides insight into cellular identities and functions.

Authors:  Sarah M Romereim; Adam F Summers; William E Pohlmeier; Pan Zhang; Xiaoying Hou; Heather A Talbott; Robert A Cushman; Jennifer R Wood; John S Davis; Andrea S Cupp
Journal:  Mol Cell Endocrinol       Date:  2016-09-28       Impact factor: 4.102

6.  Immunohistochemical localization of the bone morphogenetic protein receptors in the porcine ovary.

Authors:  Ruth L Quinn; Gail Shuttleworth; Morag G Hunter
Journal:  J Anat       Date:  2004-07       Impact factor: 2.610

7.  Yes-associated protein 1 is required for proliferation and function of bovine granulosa cells in vitro†.

Authors:  Michele R Plewes; Xiaoying Hou; Pan Zhang; Aixin Liang; Guohua Hua; Jennifer R Wood; Andrea S Cupp; Xiangmin Lv; Cheng Wang; John S Davis
Journal:  Biol Reprod       Date:  2019-11-21       Impact factor: 4.161

8.  Trafficking of cholesterol from lipid droplets to mitochondria in bovine luteal cells: Acute control of progesterone synthesis.

Authors:  Michele R Plewes; Crystal Krause; Heather A Talbott; Emilia Przygrodzka; Jennifer R Wood; Andrea S Cupp; John S Davis
Journal:  FASEB J       Date:  2020-07-02       Impact factor: 5.834

9.  PKCδ and θ possibly mediate FSH-induced mouse oocyte maturation via NOX-ROS-TACE cascade signaling pathway.

Authors:  Qian Chen; Wenqiang Zhang; Hao Ran; Lizhao Feng; Hao Yan; Xinyi Mu; Yingying Han; Wei Liu; Guoliang Xia; Chao Wang
Journal:  PLoS One       Date:  2014-10-28       Impact factor: 3.240

10.  Gap junctional proteins, connexin 26, 32, and 43 in sheep ovaries throughout the estrous cycle.

Authors:  A T Grazul-Bilska; D A Redmer; J J Bilski; A Jablonka-Shariff; V Doraiswamy; L P Reynolds
Journal:  Endocrine       Date:  1998-06       Impact factor: 3.925

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.