Fas-mediated apoptosis is suppressed by calf serum in cultured bovine luteal cells.

Calf serum (CS) is a common supplement used in cell culture. It has been suggested that CS contains substances protecting cells against apoptosis. To examine whether a culture system including CS is appropriate for studying apoptosis in bovine luteal cells, we examined the influence of CS on the expression of Fas, bcl-2 and bax gene. Since progesterone (P(4)) is known to be an anti-apoptotic factor in bovine luteal cells, the present study was carried out to examine the P(4) effect on apoptosis. Bovine mid-luteal cells were exposed to Fas ligand (Fas L) in the presence or in the absence of P(4) antagonist (onapristone, OP) in a basal medium (BM) containing 5% CS (BM-CS) or BM containing 0.1% BSA (BM-BSA). Although Fas L alone, OP alone or Fas L plus OP did not show any cytotoxic effect on the cells cultured in BM-CS, administration of OP or OP in combination with Fas L resulted in the killing of 30% and 55% of the cells cultured in BM-BSA medium, respectively (p<0.05). Concomitantly, CS inhibited bax mRNA expression and stimulated bcl-2 expression in the cells (p<0.05). Moreover, in the cells cultured with BM-CS, Fas mRNA expression was smaller than that of cells incubated in BM-BSA medium (p<0.05). The overall results suggest that CS suppressed Fas-mediated cell death in cultured bovine luteal cells by promoting the ratio of bcl-2 to bax expression and by inhibiting Fas expression. Therefore, it may be suggested that CS contains such anti-apoptotic substances (growth factors) amplifying the cell survival pathways in the bovine corpus luteum (CL) in vitro.

[1]  J. Tilly,et al.  Expression of superoxide dismutase, catalase and glutathione peroxidase in the bovine corpus luteum: evidence supporting a role for oxidative stress in luteolysis , 1995, Endocrine.

[2]  K. Okuda,et al.  Role of tumor necrosis factor-alpha and nitric oxide in luteolysis in cattle. , 2005, Domestic animal endocrinology.

[3]  B. Berisha,et al.  Ovarian function in ruminants. , 2005, Domestic animal endocrinology.

[4]  K. Okuda,et al.  Progesterone Is a Suppressor of Apoptosis in Bovine Luteal Cells1 , 2004, Biology of reproduction.

[5]  R. Harman,et al.  Progesterone receptor and the cell cycle modulate apoptosis in granulosa cells. , 2004, Endocrinology.

[6]  E. Gregoraszczuk,et al.  Effect of growth hormone and insulin-like growth factor-I on spontaneous apoptosis in cultured luteal cells collected from early, mature, and regressing porcine corpora lutea. , 2004, Animal reproduction science.

[7]  R. Harman,et al.  Cell cycle progression and activation of Akt kinase are required for insulin-like growth factor I-mediated suppression of apoptosis in granulosa cells. , 2004, Molecular endocrinology.

[8]  M. Vega,et al.  Regulation of steroid synthesis and apoptosis by insulin-like growth factor I and insulin-like growth factor binding protein 3 in human corpus luteum during the midluteal phase. , 2002, Reproduction.

[9]  A. Sirotkin,et al.  Effect of epidermal growth factor (EGF) on steroid and cyclic nucleotide secretion, proliferation and ERK-related MAP-kinase in cultured rabbit granulosa cells. , 2002, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

[10]  K. Okuda,et al.  Fas-Fas Ligand System Mediates Luteal Cell Death in Bovine Corpus Luteum1 , 2002, Biology of reproduction.

[11]  A. Sirotkin,et al.  Effect of growth factors on proliferation, apoptosis and protein kinase A expression in cultured porcine cumulus oophorus cells. , 2002, Reproduction, nutrition, development.

[12]  J. Pate,et al.  Immune cells in the corpus luteum: friends or foes? , 2001, Reproduction.

[13]  M. Paape,et al.  Escherichia coli induces apoptosis and proliferation of mammary cells , 2001, Cell Death and Differentiation.

[14]  R. Harman,et al.  Apoptosis of Bovine Granulosa Cells After Serum Withdrawal Is Mediated by Fas Antigen (CD95) and Fas Ligand1 , 2001, Biology of reproduction.

[15]  R. Harman,et al.  Regulation of Fas Antigen (Fas, CD95)-Mediated Apoptosis of Bovine Granulosa Cells by Serum and Growth Factors1 , 2000, Biology of reproduction.

[16]  N. Sugino,et al.  Expression of Bcl-2 and Bax in the human corpus luteum during the menstrual cycle and in early pregnancy: regulation by human chorionic gonadotropin. , 2000, The Journal of clinical endocrinology and metabolism.

[17]  K. Okuda,et al.  Is Tumor Necrosis Factor α a Trigger for the Initiation of Endometrial Prostaglandin F2α Release at Luteolysis in Cattle?1 , 2000 .

[18]  R. Rajamahendran,et al.  Morphological and Biochemical Identification of Apoptosis in Small, Medium, and Large Bovine Follicles and the Effects of Follicle-Stimulating Hormone and Insulin-Like Growth Factor-I on Spontaneous Apoptosis in Cultured Bovine Granulosa Cells1 , 2000, Biology of reproduction.

[19]  B. Rueda,et al.  Decreased Progesterone Levels and Progesterone Receptor Antagonists Promote Apoptotic Cell Death in Bovine Luteal Cells1 , 2000, Biology of reproduction.

[20]  D. Porter,et al.  Expression and Activity of the Fas Antigen in Bovine Ovarian Follicle Cells1 , 2000, Biology of reproduction.

[21]  R. Cowan,et al.  Expression and Function of Fas Antigen Vary in Bovine Granulosa and Theca Cells During Ovarian Follicular Development and Atresia1 , 2000, Biology of reproduction.

[22]  R. Meidan,et al.  Intraovarian regulation of luteolysis. , 2019, Journal of reproduction and fertility. Supplement.

[23]  K. Okuda,et al.  Sensitivity of bovine corpora lutea to prostaglandin F2alpha is dependent on progesterone, oxytocin, and prostaglandins. , 1999, Biology of reproduction.

[24]  J. Peluso,et al.  Progesterone maintains large rat granulosa cell viability indirectly by stimulating small granulosa cells to synthesize basic fibroblast growth factor. , 1999, Biology of reproduction.

[25]  S. Nagata,et al.  Apoptosis by Death Factor , 1997, Cell.

[26]  I. Botros,et al.  Increased bax and interleukin-1beta-converting enzyme messenger ribonucleic acid levels coincide with apoptosis in the bovine corpus luteum during structural regression. , 1997, Biology of reproduction.

[27]  J. Tilly Apoptosis and ovarian function. , 1996, Reviews of reproduction.

[28]  S. Tsai,et al.  Distinct mechanisms regulate induction of messenger ribonucleic acid for prostaglandin (PG) G/H synthase-2, PGE (EP3) receptor, and PGF2 alpha receptor in bovine preovulatory follicles. , 1996, Endocrinology.

[29]  S. Nagata,et al.  The Fas death factor , 1995, Science.

[30]  K. Riabowol,et al.  Monitoring mRNA expression by polymerase chain reaction: the "primer-dropping" method. , 1994, Analytical biochemistry.

[31]  C. McCulloch,et al.  Serum deprivation induces apoptotic cell death in a subset of Balb/c 3T3 fibroblasts. , 1994, Journal of cell science.

[32]  Gwyn T. Williams,et al.  Molecular regulation of apoptosis: Genetic controls on cell death , 1993, Cell.

[33]  A. Johnson,et al.  Apoptosis during luteal regression in cattle. , 1993, Endocrinology.

[34]  K. Okuda,et al.  A study of the central cavity in the bovine corpus luteum , 1988, Veterinary Record.