Immunohistochemical localization of 3β-hydroxysteroid dehydrogenase and P450 17α-hydroxylase during follicular and luteal development in pigs, sheep, and cows

Follicular and luteal morphology and steroidogenic function were investigated by immunohistochemistry for cytochrome P450 17 alpha-hydroxylase (P450c17) and 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) during the estrous cycle in pigs, sheep, and cows. The theca interna of all species expressed P450c17 during follicular development. In the pig, this constituted a continuous layer of cells around the follicle, but a sheath of cells lining the basement membrane appeared not to express P450c17. Neither was expression of P450c17 in ovine and bovine follicles uniform throughout the theca interna. In these two species, a beaded appearance was given by P450c17, since it was expressed in some regions but not in others. Therefore, staining for P450c17 defined functional sub-populations of cells within the theca interna of pigs, sheep, and cows. Ovulation was associated with a decrease in P450c17 in all species, but some expression persisted in theca-derived cells of developing and mature porcine CL. Expression of 3 beta-HSD in the preovulatory follicle was confined to the theca of the pig and sheep; in contrast, in the cow, it was highest in the granulosa. In general, 3 beta-HSD expression appeared to be greater in porcine than ovine or bovine follicles, the physiological relevance of which is discussed. Porcine and ovine theca continued to express 3 beta-HSD after ovulation, and granulosa-derived cells increased their 3 beta-HSD expression markedly as they luteinized in all three species. During early luteal development in pigs and sheep, theca-derived cells with high 3 beta-HSD encircled luteal lobules, but these cells appeared throughout the parenchyma of the mature CL. Luteal regression in sheep and cows was typified by the loss of many cells expressing 3 beta-HSD, whereas others, adjacent to them, appeared to be intact without loss of enzyme expression. These data further define differences in steroidogenesis during follicular and luteal development among the pig, sheep, and cow.

[1]  S. Ford,et al.  Immunocytochemical localization of cytochromes P450 17 alpha-hydroxylase and aromatase in embryonic cell layers of elongating porcine blastocysts. , 1994, Endocrinology.

[2]  W. Slanger,et al.  Steroidogenesis in the preovulatory porcine follicle. , 1994, Biology of reproduction.

[3]  P. Fricke,et al.  Evaluation of growth, cell proliferation, and cell death in bovine corpora lutea throughout the estrous cycle. , 1994, Biology of reproduction.

[4]  A. Conley,et al.  Ontogeny of steroidogenic enzyme expression in the porcine conceptus. , 1994, Journal of molecular endocrinology.

[5]  J. Zheng,et al.  Vascular development and heparin-binding growth factors in the bovine corpus luteum at several stages of the estrous cycle. , 1993, Biology of reproduction.

[6]  A. Jablonka-Shariff,et al.  Growth and cellular proliferation of ovine corpora lutea throughout the estrous cycle. , 1993, Endocrinology.

[7]  A. Voss,et al.  Levels of messenger ribonucleic acid for cytochrome P450 17 alpha-hydroxylase and P450 aromatase in preovulatory bovine follicles decrease after the luteinizing hormone surge. , 1993, Endocrinology.

[8]  A. Voss,et al.  Levels of messenger ribonucleic acid for cholesterol side-chain cleavage cytochrome P-450 and 3 beta-hydroxysteroid dehydrogenase in bovine preovulatory follicles decrease after the luteinizing hormone surge. , 1993, Endocrinology.

[9]  B. Shapiro,et al.  Changes in the expression of cytochrome P450c17 associated with ovarian cystic follicles. An immunocytochemical and enzymatic analysis of porcine ovaries , 1992, The Journal of Steroid Biochemistry and Molecular Biology.

[10]  E. Milgrom,et al.  New functional zonation in the ovary as shown by immunohistochemistry of luteinizing hormone receptor. , 1992, Endocrinology.

[11]  S. Killilea,et al.  Angiogenesis in the female reproductive system , 1992, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[12]  H. Jarry,et al.  Determination of secretion rates of estradiol, progesterone, oxytocin, and angiotensin II from tertiary follicles and freshly formed corpora lutea in freely moving sows. , 1991, Endocrinology.

[13]  A N Hirshfield,et al.  Development of follicles in the mammalian ovary. , 1991, International review of cytology.

[14]  F. Labrie,et al.  Changes in 3β-Hydroxysteroid Dehydrogenase/Δ5-Δ4 Isomerase Messenger Ribonucleic Acid, Activity and Protein Levels During the Estrous Cycle in the Bovine Ovary* , 1990 .

[15]  C. Jones Endocrine function of the placenta. , 1989, Bailliere's clinical endocrinology and metabolism.

[16]  J. McGeachie,et al.  Angiogenesis in the developing corpus luteum of pregnant rats: A stereologic and autoradiographic study , 1988, The Anatomical record.

[17]  I. Probst,et al.  Inhibitory effect of oxytocin and vasopressin on steroid release by cultured porcine luteal cells. , 1988, Endocrinology.

[18]  R. Moor,et al.  Cell signaling, permeability, and microvasculatory changes during antral follicle development in mammals. , 1986, Journal of dairy science.

[19]  M. Sholley,et al.  Endothelial mitosis during the initial stages of corpus luteum neovascularization in the cycling adult rat. , 1985, The American journal of anatomy.

[20]  H. Alila,et al.  Origin of different cell types in the bovine corpus luteum as characterized by specific monoclonal antibodies. , 1984, Biology of reproduction.

[21]  C. Meban The Cellular Basis of Mammalian Reproduction , 1981 .

[22]  R. Heap Vertebrate ovary , 1979, Nature.

[23]  V. La Ultrastructure of luteolysis induction by prostaglandin F2-alpha in the non-pregnant ewe. , 1978 .

[24]  R. Moor,et al.  DISTRIBUTION OF Δ5-3β-HYDROXYSTEROID DEHYDROGENASE ACTIVITY IN THE GRAAFIAN FOLLICLE OF THE SHEEP , 1975 .

[25]  R. Scaramuzzi,et al.  Changes in gonadotrophins, ovarian steroids and follicular morphology in sheep at oestrus. , 1972, The Journal of endocrinology.

[26]  R. Short,et al.  The corpus luteum of the sheep: effect of uterine removal during luteal regression. , 1970, Journal of reproduction and fertility.

[27]  B. Lobel,et al.  Enzymic correlates of development, secretory function and regression of follicles and corpora lutea in the bovine ovary. , 1968, Acta endocrinologica.

[28]  W. Hansel,et al.  HISTOLOGICAL STUDY OF BOVINE CORPORA LUTEA. , 1965, Journal of dairy science.

[29]  H. W. Deane,et al.  BIOCHEMICAL AND HISTOCHEMICAL STUDIES ON 3-BETA-HYDROXYSTEROID DEHYDROGENASE ACTIVITY IN THE ADRENAL GLANDS AND OVARIES OF DIVERSE MAMMALS. , 1963, Endocrinology.

[30]  V. Warbritton The cytology of the corpora lutea of the ewe , 1934 .

[31]  G. Corner On the origin of the corpus luteum of the sow from both granulosa and theca interna , 1919 .