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Mol. Cells 2011; 32(2): 203-207

Published online June 1, 2011

https://doi.org/10.1007/s10059-011-0086-7

© The Korean Society for Molecular and Cellular Biology

Regulation of the Female Rat Estrous Cycle by a Neural Cell-Specific Epidermal Growth Factor-like Repeat Domain Containing Protein, NELL2

Byung Jun Ryu, Han Rae Kim, Jin Kwon Jeong, and Byung Ju Lee*

Department of Biological Sciences, University of Ulsan, Ulsan 680-749, Korea

Correspondence to : *Correspondence: bjlee@ulsan.ac.kr

Received: April 25, 2011; Revised: May 11, 2011; Accepted: May 12, 2011

Abstract

NELL2, a protein containing epidermal growth factor-like repeat domains, is predominantly expressed in the nerv-ous system. In the mammalian brain, NELL2 expression is mostly neuronal. Previously we found that NELL2 is involved in the onset of female puberty by regulating the release of gonadotropin-releasing hormone (GnRH), and in normal male sexual behavior by controlling the development of the sexually dimorphic nucleus of the preoptic area (POA). In this study we investigated the effect of NELL2 on the female rat estrous cycle. NELL2 expression in the POA was highest during the proestrous phase. NELL2 mRNA levels in the POA were increased by estrogen treatment in ovariectomized female rats. Blocking NELL2 synthesis in the female rat hypothalamus decreased the expression of kisspeptin 1, an important regulator of the GnRH neuronal apparatus, and resulted in disruption of the estrous cycle at the diestrous phase. These results indicate that NELL2 is involved in the maintenance of the normal female reproductive cycle in mammals.

Keywords antisense oligodeoxynucleotide, estrous cycle, gonadotropin-releasing hormone, hypothalamus, kisspeptin

Article

Research Article

Mol. Cells 2011; 32(2): 203-207

Published online August 31, 2011 https://doi.org/10.1007/s10059-011-0086-7

Copyright © The Korean Society for Molecular and Cellular Biology.

Regulation of the Female Rat Estrous Cycle by a Neural Cell-Specific Epidermal Growth Factor-like Repeat Domain Containing Protein, NELL2

Byung Jun Ryu, Han Rae Kim, Jin Kwon Jeong, and Byung Ju Lee*

Department of Biological Sciences, University of Ulsan, Ulsan 680-749, Korea

Correspondence to:*Correspondence: bjlee@ulsan.ac.kr

Received: April 25, 2011; Revised: May 11, 2011; Accepted: May 12, 2011

Abstract

NELL2, a protein containing epidermal growth factor-like repeat domains, is predominantly expressed in the nerv-ous system. In the mammalian brain, NELL2 expression is mostly neuronal. Previously we found that NELL2 is involved in the onset of female puberty by regulating the release of gonadotropin-releasing hormone (GnRH), and in normal male sexual behavior by controlling the development of the sexually dimorphic nucleus of the preoptic area (POA). In this study we investigated the effect of NELL2 on the female rat estrous cycle. NELL2 expression in the POA was highest during the proestrous phase. NELL2 mRNA levels in the POA were increased by estrogen treatment in ovariectomized female rats. Blocking NELL2 synthesis in the female rat hypothalamus decreased the expression of kisspeptin 1, an important regulator of the GnRH neuronal apparatus, and resulted in disruption of the estrous cycle at the diestrous phase. These results indicate that NELL2 is involved in the maintenance of the normal female reproductive cycle in mammals.

Keywords: antisense oligodeoxynucleotide, estrous cycle, gonadotropin-releasing hormone, hypothalamus, kisspeptin

Mol. Cells
Sep 30, 2023 Vol.46 No.9, pp. 527~572
COVER PICTURE
Chronic obstructive pulmonary disease (COPD) is marked by airspace enlargement (emphysema) and small airway fibrosis, leading to airflow obstruction and eventual respiratory failure. Shown is a microphotograph of hematoxylin and eosin (H&E)-stained histological sections of the enlarged alveoli as an indicator of emphysema. Piao et al. (pp. 558-572) demonstrate that recombinant human hyaluronan and proteoglycan link protein 1 (rhHAPLN1) significantly reduces the extended airspaces of the emphysematous alveoli by increasing the levels of TGF-β receptor I and SIRT1/6, as a previously unrecognized mechanism in human alveolar epithelial cells, and consequently mitigates COPD.

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