Literature DB >> 8056157

The NCI-H295 cell line: a pluripotent model for human adrenocortical studies.

W E Rainey1, I M Bird, J I Mason.   

Abstract

The human adrenal cortex is a complex endocrine organ that secretes mineralocorticoids, glucocorticoids and adrenal androgens. These steroids arise from morphologically and biochemically distinct zones of the adrenal gland. Studying secretion of these distinct steroid hormones has, in the past, required the isolation of cells from each of the adrenocortical zones. Indeed, the lack of a human adrenocortical cell line retaining the ability to produce any of the major adrenal steroid products has slowed studies on normal and abnormal adrenal function. This obstacle has now been largely overcome with the availability of H295 cells, which represents the first adrenocortical cell line to maintain the ability, under specified conditions, to produce all the adrenocortical steroids (i.e., mineralocorticoids, glucocorticoids, and adrenal androgens). Thus, H295 cells appear to act as pluripotent adrenocortical cells capable of being directed to produce each of the zone-specific steroids. The H295 cell line should prove to be of value in studying the molecular and biochemical mechanisms controlling adrenal steroidogenesis.

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Year:  1994        PMID: 8056157     DOI: 10.1016/0303-7207(94)90277-1

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  48 in total

1.  Comparison of aldosterone production among human adrenocortical cell lines.

Authors:  T Wang; J G Rowland; J Parmar; M Nesterova; T Seki; W E Rainey
Journal:  Horm Metab Res       Date:  2012-01-20       Impact factor: 2.936

2.  Angiotensin II-regulated transcription regulatory genes in adrenal steroidogenesis.

Authors:  Damian G Romero; Elise P Gomez-Sanchez; Celso E Gomez-Sanchez
Journal:  Physiol Genomics       Date:  2010-09-28       Impact factor: 3.107

3.  Novel molecular mechanisms in the inhibition of adrenal aldosterone synthesis: Action of tolvaptan via vasopressin V2 receptor-independent pathway.

Authors:  Yusuf Ali; Kaoru Dohi; Ryuji Okamoto; Kan Katayama; Masaaki Ito
Journal:  Br J Pharmacol       Date:  2019-04-07       Impact factor: 8.739

4.  Dihydrotestosterone stimulates aldosterone secretion by H295R human adrenocortical cells.

Authors:  Licy L Yanes; Damian G Romero
Journal:  Mol Cell Endocrinol       Date:  2009-01-21       Impact factor: 4.102

5.  Type 5 17beta-hydroxysteroid dehydrogenase (AKR1C3) contributes to testosterone production in the adrenal reticularis.

Authors:  Yasuhiro Nakamura; Peter J Hornsby; Peter Casson; Ryo Morimoto; Fumitoshi Satoh; Yewei Xing; Michael R Kennedy; Hironobu Sasano; William E Rainey
Journal:  J Clin Endocrinol Metab       Date:  2009-03-31       Impact factor: 5.958

6.  A role for the circadian clock protein Per1 in the regulation of aldosterone levels and renal Na+ retention.

Authors:  Jacob Richards; Kit-Yan Cheng; Sean All; George Skopis; Lauren Jeffers; I Jeanette Lynch; Charles S Wingo; Michelle L Gumz
Journal:  Am J Physiol Renal Physiol       Date:  2013-10-23

7.  The cAMP-responsive element binding protein (CREB) regulates the expression of acid ceramidase (ASAH1) in H295R human adrenocortical cells.

Authors:  Natasha Lucki; Marion B Sewer
Journal:  Biochim Biophys Acta       Date:  2009-03-16

8.  Orexins stimulate steroidogenic acute regulatory protein expression through multiple signaling pathways in human adrenal H295R cells.

Authors:  Manjunath Ramanjaneya; Alex C Conner; Jing Chen; Peter R Stanfield; Harpal S Randeva
Journal:  Endocrinology       Date:  2008-05-01       Impact factor: 4.736

9.  Contrasting effects of eplerenone and spironolactone on adrenal cell steroidogenesis.

Authors:  P Ye; T Yamashita; D M Pollock; H Sasano; W E Rainey
Journal:  Horm Metab Res       Date:  2008-09-25       Impact factor: 2.936

Review 10.  Adaptive evolution of mammalian aromatases: lessons from Suiformes.

Authors:  A J Conley; C J Corbin; A L Hughes
Journal:  J Exp Zool A Ecol Genet Physiol       Date:  2009-06-01
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