J Vet Sci.  2008 Dec;9(4):345-349. 10.4142/jvs.2008.9.4.345.

The expression and localization of inhibin isotypes in mouse testis during postnatal development

Affiliations
  • 1Department of Veterinary Anatomy, College of Veterinary Medicine and Veterinary Medical Research Center, Chonnam National University, Gwangju 500-757, Korea. moonc@chonnam.ac.kr
  • 2Department of Veterinary Toxicology, College of Veterinary Medicine and Veterinary Medical Research Center, Chonnam National University, Gwangju 500-757, Korea.
  • 3Department of Veterinary Surgery, College of Veterinary Medicine and Veterinary Medical Research Center, Chonnam National University, Gwangju 500-757, Korea.
  • 4Department of Veterinary Obstetrics, College of Veterinary Medicine, Kyungpook National University, Daegu 702-701, Korea.
  • 5Department of Veterinary Anatomy, College of Veterinary Medicine and Applied Radiological Science Research Institute, Cheju National University, Jeju 690-756, Korea.

Abstract

Inhibin, which is important for normal gonadal function, acts on the pituitary gonadotropins to suppress folliclestimulating hormone (FSH) secretion. The level and cellular localization of the inhibin isotypes, alpha, beta(A) and beta(B), in the testis of mice were examined during postnatal development in order to determine if inhibin expression is related to testicular maturation. Mouse testes were sampled on postnatal days (PNDs) 1, 3, 6, 18, 48 and 120, and analyzed by Western blotting and immunofluorescence. Western blot analysis showed very low levels of inhibin alpha, beta(A) and beta(B) expression in the testes at days 1 to 6 after birth. The levels then increased gradually from PND 18 to 48-120, and there were significant peaks at PND 48. Inhibin alpha, beta(A) and beta(B) were detected in testicular cells during postnatal development using immunohistochemistry. The immunoreactivity of inhibin alpha was rarely observed in testicular cells during PND 1 to 6, or in the cytoplasmic process of Sertoli cells surrounding the germ cells and interstitial cells during PND 18 to 120. Inhibin beta(A) and beta(B) immunoreactivity was rarely observed in the testis from PND 1 to 6. On the other hand, it was observed in some spermatogonial cells, as well as in the interstitial space between PND 48 and PND 120. We conclude that the expression of inhibin isotypes increases progressively in the testis of mice with increasing postnatal age, suggesting that inhibin is associated with a negative feedback signal for FSH in testicular maturation.

Keyword

inhibin; mouse; postnatal development; Sertoli cell; testis

MeSH Terms

Aging/*physiology
Animals
Gene Expression Regulation/*physiology
Inhibin-beta Subunits/genetics/*metabolism
Inhibins/genetics/*metabolism
Male
Mice
Mice, Inbred ICR
Protein Isoforms/metabolism
Protein Transport/*physiology
Testis/*metabolism

Figure

  • Fig. 1 Light micrographs of the mouse testes at postnatal day (PND) 1 (A), PND 18 (B), and PND 48 (C). The arrows in A indicate gonocytes in undifferentiated seminiferous epithelium. The asterisk in C indicates the defined lumens of the tubules including mature sperm cells. H&E stain. Scale bars = 40 µm.

  • Fig. 2 Expression of inhibin isotypes α, βA and βB in mouse testis increased progressively with postnatal age. Photographs: Representative photographs of Western blots for inhibin isotypes α, βA and βB and beta-actin (A). Arrowheads indicate the positions of the inhibin isotypes (40~47 kDa) and beta-actin (45 kDa). Minor bands at various molecular weights were detected on the immunoblots for the inhibin isotypes α, βA and βB. Bar graph: The results of densitometric data analysis (mean ± SE, n = 3 mice/group). The relative expression levels of the inhibin isotypes were calculated after normalization to the beta-actin band from three different samples. The value for the testis at postnatal day (PND) 1 was arbitrarily defined as 1 (B, C and D, graphs). *p < 0.05, **p < 0.01 vs. PND 1-6.

  • Fig. 3 Immunofluorescent localization of inhibin α, βA, and βB isotypes in mouse testis at postnatal days 48. (A and B) Double-immunofluorescent staining in the same section showed the co-localization of inhibin α with vimentin in cell bodies of Sertoli cells (arrowheads), the cytoplasmic process of Sertoli cells (arrows) and in interstitial spaces (asterisks). (C) Immunofluorescent localization of the inhibin βA subunit was observed in the cell membrane of some spermatogenic cells (arrows) as well as in the interstitial cells (asterisk). (D) Immunofluorescent localization of the inhibin βB subunit was observed mainly in cell membranes of interstitial cells (asterisk) as well as in some spermatogonia (arrows). Scale bars = 30 µm.


Reference

1. Allenby G, Foster PM, Sharpe RM. Evidence that secretion of immunoactive inhibin by seminiferous tubules from the adult rat testis is regulated by specific germ cell types: correlation between in vivo and in vitro studies. Endocrinology. 1991. 128:467–476.
Article
2. Au CL, Robertson DM, de Kretser DM. Measurement of inhibin and an index of inhibin production by rat testes during postnatal development. Biol Reprod. 1986. 35:37–43.
Article
3. Buzzard JJ, Loveland KL, O'Bryan MK, O'Connor AE, Bakker M, Hayashi T, Wreford NG, Morrison JR, de Kretser DM. Changes in circulating and testicular levels of inhibin A and B and activin A during postnatal development in the rat. Endocrinology. 2004. 145:3532–3541.
Article
4. Clifton RJ, O'Donnell L, Robertson DM. Pachytene spermatocytes in co-culture inhibit rat Sertoli cell synthesis of inhibin βB-subunit and inhibin B but not the inhibin α-subunit. J Endocrinol. 2002. 172:565–574.
Article
5. de Kretser DM, Robertson DM. The isolation and physiology of inhibin and related proteins. Biol Reprod. 1989. 40:33–47.
Article
6. Guitton N, Touzalin AM, Sharpe RM, Cheng CY, Pinon-Lataillade G, Méritte H, Chenal C, Jégou B. Regulatory influence of germ cells on Sertoli cell function in the pre-pubertal rat after acute irradiation of the testis. Int J Androl. 2000. 23:332–339.
Article
7. Illingworth PJ, Groome NP, Byrd W, Rainey WE, McNeilly AS, Mather JP, Bremner WJ. Inhibin-B: a likely candidate for the physiologically important form of inhibin in men. J Clin Endocrinol Metab. 1996. 81:1321–1325.
Article
8. Jin W, Arai KY, Herath CB, Kondo M, Ishi H, Tanioka Y, Watanabe G, Groome NP, Taya K. Inhibins in the male Göttingen miniature pig: Leydig cells are the predominant source of inhibin B. J Androl. 2001. 22:953–960.
Article
9. Jin W, Wada S, Arai KY, Kishi H, Herath CB, Watanabe G, Suzuki AK, Groome NP, Taya K. Testicular secretion of inhibin in the male golden hamster (Mesocricetus auratus). J Androl. 2001. 22:207–211.
10. Lee VW, de Kretser DM, Hudson B, Wang C. Variations in serum FSH, LH and testosterone levels in male rats from birth to sexual maturity. J Reprod Fertil. 1975. 42:121–126.
Article
11. Mason AJ. Burger HG, de Kretser D, Findlay J, Igarashi M, editors. Human inhibin and activin: Structure and recombinant expression in mammalian cells. Inhibin-Non-Steroidal Regulation of Follicle Stimulating Hormone Secretion. 1987. New York: Raven Press;42–77.
12. Matzuk MM, Finegold MJ, Su JG, Hsueh AJ, Bradley A. α-inhibin is a tumour-suppressor gene with gonadal specificity in mice. Nature. 1992. 360:313–319.
Article
13. McMullen ML, Cho BN, Yates CJ, Mayo KE. Gonadal pathologies in transgenic mice expressing the rat inhibin α-subunit. Endocrinology. 2001. 142:5005–5014.
Article
14. Mellor SL, Richards MG, Pedersen JS, Robertson DM, Risbridger GP. Loss of the expression and localization of inhibin α-subunit in high grade prostate cancer. J Clin Endocrinol Metab. 1998. 83:969–975.
Article
15. Nagata S, Tsunoda N, Nagamine N, Tanaka Y, Taniyama H, Nambo Y, Watanabe G, Taya K. Testicular inhibin in the stallion: cellular source and seasonal changes in its secretion. Biol Reprod. 1998. 59:62–68.
Article
16. Noguchi J, Hikono H, Sato S, Watanabe G, Taya K, Sasamoto S, Hasegawa Y. Ontogeny of inhibin secretion in the rat testis: secretion of inhibin-related proteins from fetal Leydig cells and of bioactive inhibin from Sertoli cells. J Endocrinol. 1997. 155:27–34.
Article
17. O'Connor AE, de Kretser DM. Inhibins in normal male physiology. Semin Reprod Med. 2004. 22:177–185.
18. Pierson TM, Wang Y, DeMayo FJ, Matzuk MM, Tsai SY, O'Malley BW. Regulable expression of inhibin A in wild-type and inhibin α null mice. Mol Endocrinol. 2000. 14:1075–1085.
Article
19. Pineau C, Sharpe RM, Saunders PT, Gérard N, Jégou B. Regulation of Sertoli cell inhibin production and of inhibin α-subunit mRNA levels by specific germ cell types. Mol Cell Endocrinol. 1990. 72:13–22.
Article
20. Plant TM, Marshall GR. The functional significance of FSH in spermatogenesis and the control of its secretion in male primates. Endocr Rev. 2001. 22:764–786.
Article
21. Robertson DM, Cahir N, Findlay JK, Burger HG, Groome N. The biological and immunological characterization of inhibin A and B forms in human follicular fluid and plasma. J Clin Endocrinol Metab. 1997. 82:889–896.
Article
22. Schmitt JF, Millar DS, Pedersen JS, Clark SL, Venter DJ, Frydenberg M, Molloy PL, Risbridger GP. Hypermethylation of the inhibin α-subunit gene in prostate carcinoma. Mol Endocrinol. 2002. 16:213–220.
Article
23. Seok OS, Ahn JM, Mayo KE, Cho BN. Developmental changes in inhibin-α gene expression in the mouse testis. Mol Cells. 2004. 17:67–72.
24. Sharpe RM, Turner KJ, McKinnell C, Groome NP, Atanassova N, Millar MR, Buchanan DL, Cooke PS. Inhibin B levels in plasma of the male rat from birth to adulthood: effect of experimental manipulation of Sertoli cell number. J Androl. 1999. 20:94–101.
25. van Dissel-Emiliani FM, Grootenhuis AJ, de Jong FH, de Rooij DG. Inhibin reduces spermatogonial numbers in testes of adult mice and Chinese hamsters. Endocrinology. 1989. 125:1899–1903.
Article
26. Woodruff TK, Besecke LM, Groome N, Draper LB, Schwartz NB, Weiss J. Inhibin A and inhibin B are inversely correlated to follicle-stimulating hormone, yet are discordant during the follicular phase of the rat estrous cycle, and inhibin A is expressed in a sexually dimorphic manner. Endocrinology. 1996. 137:5463–5467.
Article
Full Text Links
  • JVS
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr