토끼에서 출생 후 고환간질세포의 발생에 관한 연구

Studies on the postnatal development of the Leydig cell in rabbits

  • 태현진 (전북대학교 수의과대학 생체안전성연구소) ;
  • 박영재 (전북대학교 수의과대학 생체안전성연구소) ;
  • 강형섭 (헬스케어 사업단) ;
  • 김남수 (헬스케어 사업단) ;
  • 박상열 (헬스케어 사업단) ;
  • 양홍현 (전북대학교 수의과대학 생체안전성연구소) ;
  • 안동춘 (강원대학교 수의학과) ;
  • 김인식 (헬스케어 사업단)
  • Tae, Hyun-Jin (College of Veterinary Medicine, Bio-Safety Research Institute, Chonbuk National University) ;
  • Park, Young-Jae (College of Veterinary Medicine, Bio-Safety Research Institute, Chonbuk National University) ;
  • Kang, Hyung-Sub (Center for Healthcare Technology Development) ;
  • Kim, Nam-Soo (Center for Healthcare Technology Development) ;
  • Park, Sang-Youel (Center for Healthcare Technology Development) ;
  • Yang, Hong-Hyun (College of Veterinary Medicine, Bio-Safety Research Institute, Chonbuk National University) ;
  • Ahn, Dong-Choon (Department of Veterinary Medicine, Kangwon National University) ;
  • Kim, In-Shik (Center for Healthcare Technology Development)
  • 심사 : 2005.08.17
  • 발행 : 2005.09.22

초록

Changes in the rabbit Leydig cell from birth to adulthood were studied in New Zealand white rabbits of 1, 7, 21, 35, 49, 70, 105, 147, 196, and 252 days (n = 8 rabbits per group) of age. The objectives of this study were to understand the fate of the fetal Leydig cells, to determine the changes in serum testosterone levels, and leutenizing hormone-stimulated testosterone production per testis in vitro, and to quantify adult Leydig cells by number and average volume with age. Testes of rabbits were fixed by whole body perfusion using a fixative containing 2.5% glutaraldehyde in cacodylate buffer, processed and embedded in Epon-araldite. Using $1{\mu}m$ sections stained with methylene blue-azure II, qualitative and quantitative (stereological) morphological studies were performed. Testosterone levels in the incubation medium of luteinizing hormone-stimulated (100 ng/ml) testosterone secretion per testis in vitro, and in serum were determined by radioimmunoassay. The average volume of a testis of 1-day-old rabbits was determined as $0.0073cm^3$ and the parameter increased linearly from birth to 252 days ($3.93cm^3$). The volume density of the seminiferous tubules increased with age from 33.76% at day 1 to 88.2% at day 252. The volume density of the interstitium represents 66.24% of the testicular parenchyma at day 1. This proportion progressively diminished during development to reach a value of 11.8% at day 252. The volume density of Leydig cells increased almost linearly from birth (0.001%) to 252 days (2.62%). Leydig cell mass per testis increases from 0.0012 mg to 0.25 mg between days 1 and 35, from 2.66 mg to 44.3 mg between days 49 and 105 and from 65.42 mg and 102.9 mg between days 147 and 252. The absolute numbers of adult Leydig cells per testis increased linearly from birth to 252 days. The average volume of adult Leydig cell on days 1, 7, 21 and 35 was not significantly different; a gradual and continued increase was observed thereafter, reaching a 3-fold increase at 196 and 252 days. Serum testosterone concentrations were not significantly different at day 1 compared days 7, 21, 35. Significant increases were observed at days 49 and 70. Values at days 70 and 105 and days 147, 196, and 252 were not significantly different. LH-stimulated testosterone production per testis in vitro was significantly different at day 1 compared days 7, 21, 35. Significant increases were observed at days 49 and 70. Hormonal values at days 105, 147, 196, and 252 were not significantly different. These data suggested Leydig cell developmental phase can be classified: a neonatal phase (1-7 days), a prepubertal phase (14-49 days) and an adult phase (70-252 days). Immature and mature adult Leydig cells, initially detected at days 7 and 49, respectively, and mature adult Leydig cells were abundant Leydig cell type according to the number and absolute volume per testis form day 49 onwards.

키워드

참고문헌

  1. Ariyaratne HBS, Mendis-Handagama SMLC. Changes in the testis interstitium Sprague Dawley rats from birth to sexual maturity. Biol Reprod 2000, 62, 680-690 https://doi.org/10.1095/biolreprod62.3.680
  2. Black VH, Christensen AK. Differentiation of interstitial cells and Sertoli cells in fetal guinea pig testis. Am J Anat 1969, 124, 211-238 https://doi.org/10.1002/aja.1001240206
  3. Blackburn WR, Chung KW, Bullock L, Bardin CW. Testicular feminization in the mouse: Studies of Leydig cell structure and function. Biol Reprod 1973, 9, 9-23 https://doi.org/10.1093/biolreprod/9.1.9
  4. Bortolussi M, Zanchetta R, Belvedere P, Clombo L. Sertoli and Leydig cell numbers and gonadotropin receptors in rat testis from birth to puberty. Cell Tissue Res 1990, 260, 185-191 https://doi.org/10.1007/BF00297504
  5. Castro AC, Berndtson WE, Cardoso FM. Plasma and testicular testosterone levels, volume density and number of Leydig cells and spermatogenic efficiency of rabbits. Braz J Med Biol Res 2002, 35, 493-498
  6. Christensen AK. The fine structure of testicular interstitial cells in guinea pigs. J Cell Biol 1965, 26, 911-935 https://doi.org/10.1083/jcb.26.3.911
  7. Chubb C, Ewing L, Irby D, Desjardins C. Testicular maturation in the rabbit. Secretion of testosterone, dihydrotestosterone, 5$\alpha$-androstan-3$\beta$, 17$\beta$‚-diol and 5$\alpha$-androstan-3$\beta$, 17$\beta$‚-diol by perfused rabbit estesepididymides and spermatogenesis. Biol Reprod 1978, 18, 212-218 https://doi.org/10.1095/biolreprod18.2.212
  8. Ewing LL, Zirkin BR. Leydig cell structure and steroidogenic function. Recent Prog Horm Res 1983, 39, 599-632
  9. Ewing LL, Zirkin BC, Cochran R.C, Kromann, N, Peters C. Testosterone secretion by rat, rabbit, guinea pig, dog, and hamster testes perfused in vitro: correlation with Leydig cell mass. Endocrinology 1979, 105, 1136-1142
  10. Fawcett DW, Neaves WB, Flores MN. Comparative observations on intertubular lymphatics and the organization of the interstitial tissue of the mammalian testis. Biol Reprod 1973, 9, 500-532 https://doi.org/10.1093/biolreprod/9.5.500
  11. Floderus S. Untersuchunger uber den bau der menschlichen hypophyse mit besonderer berucksichtigung der quantitativen mikromorphologischen verhaltnisse. Acta Pathol Microbiol Scand 1944, 5, 1-276 https://doi.org/10.1111/j.1600-0463.1928.tb05307.x
  12. Franca LR, Silva VA, Chiarini-Garcia H, Gracia SK, Debeljuk L. Cell proliferation and hormonal changes during postnatal development of the testis in the pig. Biol Reprod 2000, 63, 1629-1636 https://doi.org/10.1095/biolreprod63.6.1629
  13. Gondos B, Paup DC, Ross J, Gorskin R A. Ultrastructural differentiation of Leydig cells in the fetal and postnatal hamster testis. Anat Rec 1974, 178, 551-556 https://doi.org/10.1002/ar.1091780304
  14. Gondos B, Morrison KP, Renston RH. Leydig cell differentiation in the prepubertal rabbit testis. Biol Reprod 1977, 17, 745-748 https://doi.org/10.1095/biolreprod17.5.745
  15. Gondos B, Renston RH, Conner LA. Ultrastructure of germ cells and Sertoli cells in the postnatal rabbit testis. Am J Anat 1973, 136, 427-440 https://doi.org/10.1002/aja.1001360404
  16. Gondos B, Renston RH, Goldstein D. A. Postnatal differentiation of Leydig cells in the rabbit testis. Am J Anat 1976, 145, 167-182 https://doi.org/10.1002/aja.1001450203
  17. Johnson, L. and Neaves, W. B. Age-related changes in the Leydig cell population, seminiferous tubules, and sperm production in stallions. Biol Reprod 1981, 24, 703-712 https://doi.org/10.1095/biolreprod24.3.703
  18. Kerr JB. A light microscopic and morphometric analysis of the Sertoli cell during the spermatogenic cycle of the rat. Anat Embryol Berl 1988, 177, 341-348 https://doi.org/10.1007/BF00315842
  19. Kim IS, Ariyaratne HBS, Mendis-Handagama SMLC. Changes in the testis interstitium of Brown Norway rats with aging and effects of luteinizing and thyroid hormones on the aged testes in enhancing the steroidogenic potential. Biol Reprod 2002, 66, 1359-1366 https://doi.org/10.1095/biolreprod66.5.1359
  20. Lipsett MB, Tullner WW. Testosterone synthesis by the fetal rabbit gonad. Endocrinology 1965, 77, 273-277 https://doi.org/10.1210/endo-77-2-273
  21. Lording DW, de-Krester DM. Comparative ultrastructural and histochemical studies of the interstitial cells of the rat testis during fetal and postnatal development. J Reprod Fert 1972, 29, 261-269 https://doi.org/10.1530/jrf.0.0290261
  22. Mendis-Handagama SMLC, Ariyaratne HBS. Differentiation of the adult Leydig cell population in the postnatal testis. Biol Reprod 2001, 65, 660-671 https://doi.org/10.1095/biolreprod65.3.660
  23. Mendis-Handagama SMLC, Ewing LL. Sources of error in the estimation of Leydig cell numbers in control and atrophied mammalian testes. J Microsc 1990, 159, 73-82 https://doi.org/10.1111/j.1365-2818.1990.tb03020.x
  24. Mendis-Handagama SMLC, Risbridger GP, de Krester DM. Morphometric analysis of the components of the neonatal and the adult rat testis interstitium. Int J Androl 1987, 10, 525-534 https://doi.org/10.1111/j.1365-2605.1987.tb00352.x
  25. Mendis-Handagama SMLC, Zirkin BR, Ewing LL. Comparison of components of the testis interstitium with testosterone secretion hamster, rat, and guinea pig testes perfused in vitro. Am J Anat 1988, 188, 12-22
  26. Mori H, Christensen AK. Morphometric analysis of Leydig cells in the normal rat testis. J Cell Biol 1980, 84, 340-354 https://doi.org/10.1083/jcb.84.2.340
  27. Neaves WB. Changes in testicular Leydig cells and in plasma testosterone levels among seasonally breeding rock hyrax. Biol Reprod 1973, 8, 451-466 https://doi.org/10.1093/biolreprod/8.4.451
  28. Nistal M, Paniagua R, Regadera J, Santamaria L, Amat PA. quantitative morphological study of human Leydig cells from birth to adulthood. Cell Tissue Res 1986, 246, 229-236 https://doi.org/10.1007/BF00215884
  29. Rey RA, Campo SM, Bedecarras C. Histologic, morphometric and functional study of the seminiferous tubules of the Cebus monkey from birth to the end of puberty. J Clin Endocrinol Metab 1993, 76, 1325-1331 https://doi.org/10.1210/jc.76.5.1325
  30. Rey RA, Nagle CA, Chemes H. Morphometric study of the testicular interstitial tissue of the monkey Cebus apella during postnatal development. Tissue Cell 1996, 28, 31-42 https://doi.org/10.1016/S0040-8166(96)80042-5
  31. Rune GM, Souza DE, Merker HJ. Ultrastructural and histochemical characterization of marmoset(Callithrix jacchus) Leydig cells during postnatal development. Anat Embryol 1991, 183, 179-191
  32. Saez JM. Leydig cells: endocrine, paracrine, and autocrine regulation. Endocrine Rev 1994, 15, 576-626
  33. Sanchez B, Pizarro M, Garcia P, Flores JM. Histological study of Leydig cells in the cat from birth to sexual maturity. J Reprod Fert 1993, 47, 349-353
  34. Short RV, Mann T. The sexual cycle of a seasonally breeding mammal, the roebuck (Capreolus capreolus). J Reprod Fertil 1966, 12, 713-728
  35. Wrobel KH. The postnatal development of the bovine Leydig cell population. Reprod Domest Anim 1990, 25, 51-60 https://doi.org/10.1111/j.1439-0531.1990.tb00681.x
  36. Zirkin BR, Ewing LL, Kromann N, Cochran RC. Testosterone secretion by rat, rabbit, guinea pig, dog, and hamster testes perfused in vitro: correlation with Leydig cell ultrastructure. Endocrinology 1980, 6, 1868-1874