Browse > Article
http://dx.doi.org/10.15616/BSL.2019.25.1.107

Expression of Fas and TNFR1 in the Luteal Cell Types Isolated from the Ovarian Corpus Luteum  

Kim, Minseong (College of Animal Life Sciences, Kangwon National University)
Lee, Sang-Hee (Discipline of ICT, School of Technology, Environments and Design, University of Tasmania)
Lee, Seunghyung (College of Animal Life Sciences, Kangwon National University)
Kim, Gur-Yoo (College of Animal Life Sciences, Kangwon National University)
Abstract
The corpus luteum (CL) is composed to various cells, such as luteal steroidogenic cells (LSCs), luteal thecal steroidogenic cells (LTCs), luteal endothelial cells (LECs), fibroblast, immune cells and blood cells. The life span of CL is controlled by proliferation and apoptosis of luteal cells. Therefore, this study investigated apoptotic factors in luteal cells derived from bovine CL. The CL tissues were collected from bovine ovaries and luteal cells were isolated from middle phase CL. Then, LTCs and LECs were separated according to cellular morphology from LSCs. The expression of Bax, Bcl-2, Fas and tumor necrosis factor 1 receptor (TNF1R) mRNA and protein were analyzed using quantitative RT-PCR and western blot. Results show that, Bax and TNFR1 mRNA expression were significantly increased at late group than early and middle groups, otherwise Bcl-2 were significantly decreased at late group than early group (P<0.05). Fas mRNA expression were significantly decreased in middle group compared to early and late groups (P<0.05). In addition, Bax and Bcl-2 mRNA in LTCs was lower than LSCs, Fas mRNA was higher than LSCs. The Bcl-2 protein expression was lower at LTCs than LSCs, especially Fas protein in LTCs was significantly lower than LSCs and LECs (P<0.05). Otherwise, TNFR1 protein of LTCs were similar with LSCs but higher compared with LECs. In conclusion, we suggest that the results may help understanding of apoptosis ability in luteal cells according to cell type during CL regression of estrous cycle.
Keywords
Corpus luteum; Luteal steroidogenic cells; Luteal thecal steroidogenic cells; Apoptosis;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
연도 인용수 순위
1 Berisha B, Schams D, Rodler D, Pfaffl MW. Angiogenesis in the ovary-the most important regulatory event for follicle and corpus luteum development and function in cow-an overview. Anatomia, Histologia, Embryologia. 2016. 45: 124-130.   DOI
2 Chouhan V, Dangi S, Gupta M, Babitha V, Khan F, Panda R, Yadav V, Singh G, Sarkar M. Stimulatory effect of vascular endothelial growth factor on progesterone production and survivability of cultured bubaline luteal cells. Animal Reproduction Science. 2014. 148: 251-259.   DOI
3 Davis JS, Rueda BR. The corpus luteum: An ovarian structure with maternal instincts and suicidal tendencies. Frontiers in Bioscience. 2002. 7: d1949-d1978.   DOI
4 Davis JS, Rueda BR, Spanel-Borowski K. Microvascular endothelial cells of the corpus luteum. Reproductive Biology and Endocrinology. 2003. 1: 89.   DOI
5 Abulafia O, Sherer DM. Angiogenesis of the ovary. American Journal of Obstetrics and Gynecology. 2000. 182: 240-246.   DOI
6 Benyo DF, Pate JL. Tumor necrosis factor-alpha alters bovine luteal cell synthetic capacity and viability. Endocrinology. 1992. 130: 854-860.   DOI
7 Devoto L, Fuentes A, Kohen P, Cespedes P, Palomino A, Pommer R, Munoz A, Strauss III JF. The human corpus luteum: Life cycle and function in natural cycles. Fertility and Sterility. 2009. 92: 1067-1079.   DOI
8 Gwon SY, Rhee KJ, Lee S. Endothelial cells isolated from the bovine corpus luteum synthesize prostaglandin $f2{\alpha}$ receptor. Biomedical Science Letter. 2013. 19: 261-265.
9 Han H-I, Lee S-H, Park C-K. Development of in vitro embryo production system using collagen matrix gel attached with vascular endothelial growth factor derived from interleukin-1 beta-treated porcine endometrial tissue. Tissue Engineering Part C: Methods. 2017. 23: 396-403.   DOI
10 Kim M, Lee S-H, Lee S. Expression of H-ras, RLIP76 mRNA and protein, and angiogenic receptors in corpus luteum tissues during estrous cycles. Korean Journal of Clinical Laboratory Science. 2018. 50: 457-461.   DOI
11 Kuranaga E, Kanuka H, Furuhata Y, Yonezawa T, Suzuki M, Nishihara M, Takahashi M. Requirement of the fas ligandexpressing luteal immune cells for regression of corpus luteum. FEBS Letters. 2000. 472: 137-142.   DOI
12 Lee S, Acosta TJ, Nakagawa Y, Okuda K. Role of nitric oxide in the regulation of superoxide dismutase and prostaglandin $f2{\alpha}$ production in bovine luteal endothelial cells. Journal of Reproduction and Development. 2010. 56: 454-459.   DOI
13 Lei Z, Chegini N, Rao CV. Quantitative cell composition of human and bovine corpora lutea from various reproductive states. Biology of Reproduction. 1991. 44: 1148-1156.   DOI
14 Miyamoto Y, Skarzynski DJ, Okuda K. Is tumor necrosis factor $\alpha$ a trigger for the initiation of endometrial prostaglandin $f2{\alpha}$ release at luteolysis in cattle? Biology of Reproduction. 2000. 62: 1109-1115.   DOI
15 Neuvians T, Berisha B, Schams D. Vascular endothelial growth factor (vegf) and fibroblast growth factor (fgf) expression during induced luteolysis in the bovine corpus luteum. Molecular Reproduction and Development. 2004. 67: 389-395.   DOI
16 Skarzynski DJ, Okuda K. Sensitivity of bovine corpora lutea to prostaglandin $f2{\alpha}$ is dependent on progesterone, oxytocin, and prostaglandins. Biology of Reproduction. 1999. 60: 1292-1298.   DOI
17 Penny L, Armstrong D, Bramley T, Webb R, Collins R, Watson E. Immune cells and cytokine production in the bovine corpus luteum throughout the oestrous cycle and after induced luteolysis. Journal of Reproduction and Fertility. 1999. 115: 87-96.   DOI
18 Sakumoto R, Berisha B, Kawate N, Schams D, Okuda K. Tumor necrosis factor-$\alpha$ and its receptor in bovine corpus luteum throughout the estrous cycle. Biology of Reproduction. 2000. 62: 192-199.   DOI
19 Schams D, Berisha B. Regulation of corpus luteum function in cattle-an overview. Reproduction in Domestic Animals. 2004. 39: 241-251.   DOI
20 Shirasuna K, Nitta A, Sineenard J, Shimizu T, Bollwein H, Miyamoto A. Vascular and immune regulation of corpus luteum development, maintenance, and regression in the cow. Domestic Animal Endocrinology. 2012. 43: 198-211.   DOI
21 Stocco C, Telleria C, Gibori G. The molecular control of corpus luteum formation, function, and regression. Endocrine Reviews. 2007. 28: 117-149.   DOI
22 Tamanini C, De Ambrogi M. Angiogenesis in developing follicle and corpus luteum. Reproduction in Domestic Animals. 2004. 39: 206-216.   DOI
23 Taniguchi H, Yokomizo Y, Okuda K. Fas-fas ligand system mediates luteal cell death in bovine corpus luteum. Biology of Reproduction. 2002. 66: 754-759.   DOI
24 Zheng J, Fricke PM, Reynolds LP, Redmer DA. Evaluation of growth, cell proliferation, and cell death in bovine corpora lutea throughout the estrous cycle. Biology of Reproduction. 1994. 51: 623-632.   DOI
25 Tomac J, Cekinovic D, Arapovic J. Biology of the corpus luteum. Periodicum Biologorum. 2011. 113: 43-49.
26 Yoshioka S, Abe H, Sakumoto R, Okuda K. Proliferation of luteal steroidogenic cells in cattle. PLoS One. 2013. 8: e84186.   DOI