Literature DB >> 7604982

Neonatal hypothyroidism causes delayed Sertoli cell maturation in rats treated with propylthiouracil: evidence that the Sertoli cell controls testis growth.

L R De França1, R A Hess, P S Cooke, L D Russell.   

Abstract

BACKGROUND: The testes of rats treated neonatally with propylthiouracil (PTU) grow to almost twice their normal size. The cause of testicular enlargement has been suggested to be the result of delayed maturation of Sertoli cells, allowing Sertoli cell division to occur beyond the 15th postnatal day, the commonly recognized cutoff date for Sertoli cell divisions. It has been shown that an increased population of Sertoli cells in postnatal development supports increased numbers of germ cells in adult animals. After examining developing rats treated neonatally with PTU, we hypothesized that an approximate 10-day delay in maturation was occurring and proceeded to test this hypothesis experimentally. Thus the purpose of this report was to determine if a 10-day delay in maturation could explain the increased numbers of Sertoli cells and increased testis size in PTU-treated animals.
METHODS: Both control animals and animals treated neonatally with PTU N = 5/group were sacrificed at 15 and 25 days of age and prepared for electron microscopy.
RESULTS: Micrographs show and morphometric ultrastructural analysis of numerous parameters demonstrated at the 95% probability level that Sertoli cells from 25-day-old PTU animals are not different in size and most constituents (volume and surface area) from 15-day-old control animals and are less mature than 25-day-old control animals. Mitosis of Sertoli cells was observed in PTU-treated animals in 25-day-old animals but not in age-matched controls. The number of Sertoli cells in 25-day-old PTU-treated animals is significantly increased over age-matched controls. Micrographs show the presence of immature Sertoli cell nuclei in 25-day-old animals receiving PTU as well as increased germ cell degeneration in this group. Sertoli cell tight junction formation is also delayed in PTU-treated animals as compared with controls.
CONCLUSIONS: Together, the data show that delayed maturation of Sertoli cells occurs in treated animals that corresponds to a minimum of 10 developmental days. In the immature state, Sertoli cells continue to divide. Data presented herein and published data related to PTU treatment indicate that delayed maturation of the Sertoli cell results in delayed maturation and proliferation of other testicular cell types. From this and from published data, the hypothesis is presented that the Sertoli cell is responsible for the overall control of testis development.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7604982     DOI: 10.1002/ar.1092420108

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  22 in total

Review 1.  Implications of Sertoli cell induced germ cell apoptosis to testicular pathology.

Authors:  Caitlin J Murphy; John H Richburg
Journal:  Spermatogenesis       Date:  2015-01-26

2.  Enhanced sperm production in bulls following transient induction of hypothyroidism during pre-pubertal development.

Authors:  Muhammad S Waqas; Michela Ciccarelli; Melissa J Oatley; Amy V Kaucher; Ahmed Tibary; Jon M Oatley
Journal:  J Anim Sci       Date:  2018-12-20       Impact factor: 3.159

3.  Phthalate esters affect maturation and function of primate testis tissue ectopically grafted in mice.

Authors:  Jose R Rodriguez-Sosa; Alla Bondareva; Lin Tang; Gleide F Avelar; Krysta M Coyle; Mark Modelski; Whitney Alpaugh; Alan Conley; Katherine Wynne-Edwards; Luiz R França; Stuart Meyers; Ina Dobrinski
Journal:  Mol Cell Endocrinol       Date:  2014-10-27       Impact factor: 4.102

4.  mTORC1/rpS6 signaling complex modifies BTB transport function: an in vivo study using the adjudin model.

Authors:  Ming Yan; Linxi Li; Baiping Mao; Huitao Li; Stephen Y T Li; Dolores Mruk; Bruno Silvestrini; Qingquan Lian; Renshan Ge; C Yan Cheng
Journal:  Am J Physiol Endocrinol Metab       Date:  2019-05-21       Impact factor: 4.310

5.  Postnatal testis development, Sertoli cell proliferation and number of different spermatogonial types in C57BL/6J mice made transiently hypo- and hyperthyroidic during the neonatal period.

Authors:  Sarah Alves Auharek; Luiz Renato de França
Journal:  J Anat       Date:  2010-05       Impact factor: 2.610

Review 6.  Receptors and signaling pathways involved in proliferation and differentiation of Sertoli cells.

Authors:  Thaís Fg Lucas; Aline R Nascimento; Raisa Pisolato; Maristela T Pimenta; Maria Fatima M Lazari; Catarina S Porto
Journal:  Spermatogenesis       Date:  2014-02-20

Review 7.  The blood-testis barrier and its implications for male contraception.

Authors:  C Yan Cheng; Dolores D Mruk
Journal:  Pharmacol Rev       Date:  2011-10-28       Impact factor: 25.468

8.  The Type 3 Deiodinase Is a Critical Determinant of Appropriate Thyroid Hormone Action in the Developing Testis.

Authors:  M Elena Martinez; Aldona Karaczyn; J Patrizia Stohn; William T Donnelly; Walburga Croteau; Robin P Peeters; Valerie A Galton; Douglas Forrest; Donald St Germain; Arturo Hernandez
Journal:  Endocrinology       Date:  2016-01-04       Impact factor: 4.736

9.  Effects of concomitant diabetes mellitus and hyperthyroidism on testicular and epididymal histoarchitecture and steroidogenesis in male animals.

Authors:  Nazar Ali Korejo; Quan-Wei Wei; Atta Hussain Shah; Fang-Xiong Shi
Journal:  J Zhejiang Univ Sci B       Date:  2016 Nov.       Impact factor: 3.066

10.  Endocrine modulation of the recipient environment affects development of bovine testis tissue ectopically grafted in mice.

Authors:  Jose R Rodriguez-Sosa; Guilherme M J Costa; Rahul Rathi; Luiz R França; Ina Dobrinski
Journal:  Reproduction       Date:  2012-05-01       Impact factor: 3.906

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.