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Cited by 152Sperm and Testicular FunctionSexual Differentiation and DisordersHypothalamic control of reproductive hormones

The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.

Cellular Localization of Rat Testicular Aromatase Activity during Development

TSAI-MORRIS, CHON-HWA, AQUILANO, DANIEL R., DUFAU, MARIA L.·1985·Endocrinology
DOI 10.1210/endo-116-1-38
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Abstract

The aromatase activity from purified testicular sources (Leydig and Sertoli cells) of immature (5- and 15-day-old) and adult rats (60-day-old) was investigated by the tritiated water release method in isolated Leydig and Sertoli cells that were morphologically and functionally characterized. Electron micrographs of Sertoli cell preparations from different ages showed no marked changes, except that tight junctions between Sertoli cells normally present in 60-day-old rats were not observed in 5-day-old and rarely found in 15-day-old animals. Leydig cells underwent ultrastructural changes along with development, such as the appearance of thicker nuclear heterochromatin and laminar-like mitochondria. The 15-day-old rat interstitial tissue possessed less than 10% of Leydig cells morphologically similar to those present in the adult, whereas the rest were probably transition cells, since they did not show typical Leydig cell structure but were able to bind [125I]iodo-hCG, as evaluated by autoradiography. The number of LH/hCG-binding sites increased with age in Leydig cells, but was not detectable in Sertoli cells. The highest number of FSH-binding sites in Sertoli cells was observed in the 15-day-old animals. Minor FSH binding was found in Leydig cell preparations, which was consistent with the known LH contamination of the human FSH tracer preparation. cAMP production increased significantly in Leydig cells only after hCG treatment and in Sertoli cells after FSH stimulation. Both types of cells were shown to have the capacity for aromatization. The aromatase activity increased in the Leydig cell but decreased in the Sertoli cell during testicular development. The highest aromatase activity was found in adult rat Leydig cells, and the enzyme activity was significantly higher (2-fold) in purified Leydig cells than in crude interstitial cell preparations. Estradiol production in response to hCG stimulation in vitro was not different from the basal value in 5-day-old rat Leydig cells, but increased significantly in 60-day-old rat Leydig cells. In conclusion, 1) Leydig cells are the major site of estrogen synthesis in adult rat testis; and 2) the low aromatase activity observed in immature rat Leydig cells could partially explain the differential response of the mature and immature rat testis to hCG-induced desensitization.

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Metadata

Authors
TSAI-MORRIS, C.-H., AQUILANO, D. R., & DUFAU, M. L.
Affiliations
National Institutes of Health (US)
ORCID
Venue
Endocrinology
Publisher
The Endocrine Society
Published
1985-01
Volume
116
Issue
1
Pages
38-46
ISSN
  • 0013-7227 (ISSN-L)
  • 1945-7170
DOI
10.1210/endo-116-1-38
OpenAlex
W2122696678
Cited by
152
References
46
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2021: 1 · 2020: 2 · 2019: 2 · 2018: 2 · 2017: 3 · 2015: 3 · 2014: 1 · 2013: 2 · 2012: 2
FWCI
6.31
Type
journal article
Language
en
Open access
closed
Locations
  • Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Reproductive Medicine › Sperm and Testicular Function
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Sexual Differentiation and Disorders
  • Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
Keywords
aromatase, Leydig cells, Sertoli cells, testicular development, Leydig cell differentiation, estrogen synthesis, FSH binding, cAMP production, estradiol production, immature testis, rats
MeSH terms
Cyclic AMP, Aging, Animals, Aromatase, Estradiol, Chorionic Gonadotropin, Leydig Cells, Male, Microscopy, Electron, Oxidoreductases, Rats, Inbred Strains, Receptors, Cell Surface, Receptors, FSH, Receptors, LH, Sertoli Cells, Testis, Testosterone, Rats

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