Use este identificador para citar ou linkar para este item: https://repositorio.inpa.gov.br/handle/1/15800
Título: Sertoli cells are capable of proliferation into adulthood in the transition region between the seminiferous tubules and the rete testis in Wistar rats
Autor: Figueiredo, Andre´ Felipe Almeida
França, Luiz Renato de
Hess, Rex Allen
Costa, Guilherme M.J.
Palavras-chave: Androgen Receptor
Broxuridine
Ki 67 Antigen
Protein P27
Transcription Factor Gata 4
Androgen Receptor
Biological Marker
Broxuridine
Ki 67 Antigen
Transcription Factor Gata 4
Adult
Adulthood
Animals Cell
Animals Experiment
Cell Differentiation
Cell Proliferation
Male
Nonhuman
Phenotype
Prepuberty
Protein Expression
Rat
Rete Testis
Seminiferous Tubule
Sertoli Cell
Testis Function
Aging
Animals
Cell Proliferation
Cytology
Fluorescent Antibody Technique
Metabolism
Physiology
Rete Testis
Seminiferous Tubule
Sertoli Cell
Sexual Maturation
Wistar Rat
Aging
Animal
Biomarkers
Bromodeoxyuridine
Cell Differentiation
Cell Proliferation
Fluorescent Antibody Technique
Gata4 Transcription Factor
Ki 67 Antigen
Male
Rats, Wistar
Receptors, Androgen
Rete Testis
Seminiferous Tubules
Sertoli Cells
Sexual Maturation
Data do documento: 2016
Revista: Cell Cycle
É parte de: Volume 15, Número 18, Pags. 2486-2496
Abstract: Sertoli cells (SCs) play a crucial role in testis differentiation, development and function, determining the magnitude of sperm production in sexually mature animals. For over 40 years, it has been considered that these key testis somatic cells stop dividing during early pre-pubertal phase, between around 10 to 20 days after birth respectively in mice and rats, being after that under physiological conditions a stable and terminally differentiated population. However, evidences from the literature are challenging this dogma. In the present study, using several important functional markers (Ki-67, BrdU, p27, GATA-4, Androgen Receptor), we investigated the SC differentiation status in 36 days old and adult Wistar rats, focusing mainly in the transition region (TR) between the seminiferous tubules (ST) and the rete testis. Our results showed that SCs in TR remain undifferentiated for a longer period and, although at a lesser degree, even in adult rats proliferating SCs were observed in this region. Therefore, these findings suggest that, different from the other ST regions investigated, SCs residing in the TR exhibit a distinct functional phenotype. These undifferentiated SCs may compose a subpopulation of SC progenitors that reside in a specific microenvironment capable of growing the ST length if needed from this particular testis region. Moreover, our findings demonstrate an important aspect of testis function in mammals and opens new venues for other experimental approaches to the investigation of SC physiology, spermatogenesis progression and testis growth. Besides that, the TR may represent an important site for pathophysiological investigations and cellular interactions in the testis. © 2016 Taylor & Francis.
DOI: 10.1080/15384101.2016.1207835
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