Differential roles of estrogen receptors, ESR1 and ESR2, in adult rat spermatogenesis

Spermatogenesis is a complex and coordinated process leading to the formation of spermatozoa. This event, which is under the control of numerous endocrine and paracrine factors, seems to also be controlled by estrogens which exert their effects via nuclear estrogen receptors (ESRs) ESR1 and ESR2. Estrogens are synthesized by aromatase which is biologically expressed in the rat testis. The objective of our study was to clarify the gene expression patterns of aromatase and ESRs according to age and in the two compartments of the adult rat testis. In the adult, transcripts of aromatase vary according to the germ cell type and to the stages of seminiferous epithelium, a maximum being observed at stage I. The ESR1 gene is highly expressed in the adult testis and in stages from VIIc–d to XIV. Moreover, both ESR mRNA levels are higher in purified round spermatids than in pachytene spermatocytes, suggesting a putative role of estrogens in the haploid steps of spermatogenesis. The variability of the results in the expression of both ESRs led us to explore the putative presence of variants in the rat testis. Concerning ESR1, we have shown the presence of the full-length form and of one isoform with exon 4 deleted. For ESR2, besides the wild type, three isoforms were observed: one with exon 3 deleted, another with an insertion of 54 nucleotides, and the last one with both modifications. Therefore, the stage-regulated expression of aromatase and ESR1 genes in the rat testis suggests a likely role of estrogens in spermatogenesis.

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An exchange assay for estrogen receptors in cell nuclei of the adult rat brain

Steroids ◽

10.1016/0039-128x(77)90055-1 ◽

1977 ◽

Vol 30 (5) ◽

pp. 657-669 ◽

Cited By ~ 91

Author(s):

E ROY ◽

B MCEWEN

Keyword(s):

Estrogen Receptors ◽

Rat Brain ◽

Cell Nuclei ◽

Adult Rat ◽

Adult Rat Brain

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Differential expression of estrogen receptors α and β in adult rat accessory sex glands and lower urinary tract

Molecular and Cellular Endocrinology ◽

10.1016/s0303-7207(00)00233-1 ◽

2000 ◽

Vol 164 (1-2) ◽

pp. 109-116 ◽

Cited By ~ 44

Author(s):

Sari Mäkelä ◽

Leena Strauss ◽

George Kuiper ◽

Eeva Valve ◽

Saija Salmi ◽

...

Keyword(s):

Urinary Tract ◽

Estrogen Receptors ◽

Differential Expression ◽

Lower Urinary Tract ◽

Adult Rat ◽

Accessory Sex Glands ◽

Lower Urinary

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Immunoenzymatic demonstration of the simultaneous presence of transferrin, hemopexin and albumin in a same hepatocyte and their ultrastructural localization

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100081309 ◽

1978 ◽

Vol 36 (2) ◽

pp. 88-89

Author(s):

M. Kraemer ◽

J. Foucrier ◽

J. Vassy ◽

M.T. Chalumeau

Keyword(s):

Plasma Proteins ◽

Rat Hepatocytes ◽

Ultrastructural Localization ◽

Carrier Proteins ◽

Normal Cells ◽

Adult Rat ◽

Adult Rat Hepatocytes ◽

Monospecific Antisera ◽

Different Levels

Some authors using immunofluorescent techniques had already suggested that some hepatocytes are able to synthetize several plasma proteins. In vitro studies on normal cells or on cells issued of murine hepatomas raise the same conclusion. These works could be indications of an hepatocyte functionnal non-specialization, meanwhile the authors never give direct topographic proofs suitable with this hypothesis.The use of immunoenzymatic techniques after obtention of monospecific antisera had seemed to us useful to bring forward a better knowledge of this problem. We have studied three carrier proteins (transferrin = Tf, hemopexin = Hx, albumin = Alb) operating at different levels in iron metabolism by demonstrating and localizing the adult rat hepatocytes involved in their synthesis.Immunological, histological and ultrastructural methods have been described in a previous work.

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Expression of laminin and beta-1 integrin in embryonic, neonatal, and adult rat heart

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100085216 ◽

1991 ◽

Vol 49 ◽

pp. 182-183

Author(s):

R.L. Price ◽

T.K. Borg ◽

L. Terracio ◽

M. Nakagawa

Keyword(s):

Temporal Expression ◽

Qualitative And Quantitative ◽

Adult Rat ◽

Cytoplasmic Face ◽

Extracellular Matrix Components ◽

Basement Membrane Component ◽

Beta 1 Integrin ◽

Quantitative Changes ◽

Cytoskeletal Elements ◽

External Face

Little is known about the temporal expression of extracellular matrix components (ECM) and its receptors during development of the heart. Recent reports have shown that ECM components undergo both qualitative and quantitative changes during development, and it is believed that ECM components are important in the regulation of cell migration and cell:cell and cell:ECM recognition and adhesion.Integrins are transmembrane glycoproteins which bind several ECM components on their external face and cytoskeletal elements on the cytoplasmic face. Laminin is a basement membrane component which has been recognized as an important site for cell adhesion. Both the integrins and laminin are expressed early in development and continue to be expressed in the adult heart. With their documented roles in cell recognition, and cell:cell and cell:ECM migration and adhesion these proteins appear to be important components in development of the heart, and their temporal expression may play a pivotal role in morphogenesis and myofibrillogenesis of the heart.

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