Effects of lipopolysaccharide (LPS) and peptidoglycan (PGN) on estradiol production in bovine granulosa cells from small and large follicles

Toxicology in Vitro

Volumn 26, Issue 7, 2012, Pages 1134-1142

  Shimizu, T ^a   Miyauchi, K ^a   Shirasuna, K ^a   Bollwein, H ^b   Magata, F ^a   Murayama, C ^a   Miyamoto, A ^a  

^a OBIHIRO UNIVERSITY OF AGRICULTURE AND VETERINARY MEDICINE   (Japan)

^b UNIVERSITY OF VETERINARY MEDICINE HANNOVER   (Germany)

Author keywords

Cow; Estradiol; Granulosa cell; LH receptor; Lipopolysaccharide; Peptidoglycan

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 4; CD14 ANTIGEN; ESTRADIOL; LIPOPOLYSACCHARIDE; PEPTIDOGLYCAN; PROGESTERONE; PROTEIN MD 2; TOLL LIKE RECEPTOR 4;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CARBOHYDRATE ANALYSIS; CD14 GENE; CELL FUNCTION; CELL SURVIVAL; CELLULAR DISTRIBUTION; CONCENTRATION RESPONSE; COW; CULTURE MEDIUM; DEVELOPMENTAL STAGE; FEMALE; GENE; GENE EXPRESSION REGULATION; GRANULOSA CELL; HORMONE INHIBITION; HORMONE SYNTHESIS; IN VITRO STUDY; LARGE OVARY FOLLICLE; MD2 GENE; NOD1 GENE; NONHUMAN; NUCLEOTIDE SEQUENCE; OVARY FOLLICLE; OVARY FOLLICLE DEVELOPMENT; SMALL OVARY FOLLICLE; TLR4 GENE;

ANIMALS; ANTIGENS, CD14; BACTERIAL INFECTIONS; CATTLE; CATTLE DISEASES; CELL SURVIVAL; CELLS, CULTURED; DRUG THERAPY, COMBINATION; ESTRADIOL; FEMALE; FOLLICLE STIMULATING HORMONE; GENE EXPRESSION; GRANULOSA CELLS; LIPOPOLYSACCHARIDES; LYMPHOCYTE ANTIGEN 96; NOD1 SIGNALING ADAPTOR PROTEIN; OVARIAN FOLLICLE; PEPTIDOGLYCAN; POSTPARTUM PERIOD; TOLL-LIKE RECEPTOR 4; UTERINE DISEASES; UTERUS;

BOVINAE;

EID: 84866018682     PISSN: 08872333     EISSN: 18793177     Source Type: Journal    
DOI: 10.1016/j.tiv.2012.06.014     Document Type: Article

References (18)

1. Bagna B., Garverick H.A. Expression of steroidogenic enzyme and gonadotropin receptor genes in bovine follicles during ovarian follicular waves: a review. J. Anim. Sci. 1998, 76:1903-1921.
2. Battaglia D.F., Krasa H.B., Padmanabhan V., Viguie C., Karsch F.J. Endocrine alterations that underlie endotoxin-induced disruption of the follicular phase in ewes. Biol. Reprod. 2000, 62:45-53.
3. Herath S., Williams E.J., Lilly S.T., Gilbert R.O., Dobson H., Bryant C.E., Sheldon I.M. Ovarian follicular cells have innate immune capabilities that modulate their endocrine function. Reproduction 2007, 134:683-693.
4. Huszenicza G., Fodor M., Gacs M., Kulscar M., Dohmen M.J.W., Vamos M., Porkolab L., Kegl T., Bartyik J., Lohuis J.C.A.M., Janosi S., Szita G. Uterine bacteriology, resumption of cyclic ovarian activity and fertility in postpartum cows kept in large-scale dairy herds. Reprod. Domest. Anim. 1999, 34:237-245.
5. Jiang Q., Akashi S., Miyake K., Petty H.R. Lipopolysaccharide induces physical proximity between CD14 and toll-like receptor 4 (TLR4) prior to nuclear translocation of NF-B. J. Immunol. 2000, 165:3541-3544.
6. Karsch F.J., Battaglia D.F., Breen K.M., Debus N., Harris T.G. Mechanisms for ovarian cycle disruption by immune/inflammatory stress. Stress 2002, 5:101-112.
7. LeBlanc S.J., Duffield T.F., Leslie K.E., Bateman K.G., Keefe G.P., Walton J.S., Johnson W.H. Defining and diagnosing postpartum clinical endometritis and its impact on reproductive performance in dairy cows. J. Dairy Sci. 2002, 85:2223-2236.
8. Mateus L., Lopes da Costa L., Diniz P., Ziecik A.J. Relationship between endotoxin and prostaglandin (PGE2 and PGFM) concentrations and ovarian function in dairy cows with puerperal endometritis. Anim. Reprod. Sci. 2003, 76:143-154.
9. Meidan R., Girsh E., Blum O., Aberdam E. In vitro differentiation of bovine theca and granulosa cells into small and large luteal-like cells: morphological and functional characteristics. Biol. Reprod. 1990, 43:913-921.
10. Miyamoto A., Okuda K., Schweigert F.J., Schams D. Effects of basic fibroblast growth factor, transforming growth factor-beta and nerve growth factor on the secretory function of the bovine corpus luteum in vitro. J. Endocrinol. 1992, 135:103-114.
11. Peter A.T., Bosu W.T.K., DeDecker R.L. Suppression of preovulatory luteinizing hormone surges in heifers after intrauterine infections of Escherichia coli endotoxin. Am. J. Vet. Res. 1989, 50:368-373.
12. Peter A.T., Bosu W.T.K., Gilbert R.O. Absorption of Escherichia coli endotoxin (lipopolysaccharide) from the uteri of postpartum dairy cows. Theriogenology 1990, 33:1011-1014.
13. Petit T., Spergser J., Rosengarten R., Aurich J. Prevalence of potentially pathogenic bacteria as genital pathogens in dairy cattle. Reprod. Dom. Anim. 2009, 44:88-91.
14. Schumann R.R., Leong S.R., Flaggs G.W., Gray P.W., Wright S.D., Mathison J.C., Tobias P.S., Ulevitch R.J. Structure and function of lipopolysaccharide binding protein 1990, Science, 249, 1429-1431.
15. Sheldon I.M., Dobson H. Postpartum uterine health in cattle. Anim. Reprod. Sci. 2004, 82:295-306.
16. Sheldon I.M., Noakes D.E., Rycroft A.N., Pfeiffer D.U., Dobson H. Influence of uterine bacterial contamination after parturition on ovarian dominant follicle selection and follicle growth and function in cattle. Reproduction 2002, 123:837-845.
17. Zweigner J., Gramm H.J., Singer O.C., Wegscheider K., Schumann R.R. High concentrations of lipopolysaccharide-binding protein in serum of patients with severe sepsis or septic shock inhibit the lipopolysaccharide response in human monocytes. Blood 2001, 98:3800-3808.
18. Williams E.J., Fischer D.P., Noakes D.E., England G.C., Rycroft A., Dobson H., Sheldon I.M. The relationship between uterine pathogen growth density and ovarian function in the postpartum dairy. Theriogenology 2007, 68:549-559.