Document Detail


Androgen profiles during pubertal Leydig cell development in mice.
MedLine Citation:
PMID:  20453159     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Postnatal Leydig cell (LC) development in mice has been assumed empirically to resemble that of rats, which have characteristic hormonal profiles at well-defined maturational stages. To characterize the changes in LC function and gene expression in mice, we examined reproductive hormone expression from birth to 180 days, and quantified in vivo and in vitro production of androgens during sexual maturation. Although the overall plasma androgen and LH profiles from birth through puberty were comparable to that of rats, the timing of developmental changes in androgen production and steroidogenic capacity of isolated LCs differed. In mice, onset of androgen biosynthetic capacity, distinguished by an acute rise in androstenedione and testosterone production and an increased expression of the steroidogenic enzymes, cytochrome P450 cholesterol side-chain cleavage enzyme and 17alpha-hydroxylase, occurred at day 24 (d24) rather than at d21 as reported in rats. Moreover, in contrast to persistently high testosterone production by pubertal and adult rat LCs, testosterone production was maximal at d45 in mice, and then declined in mature LCs. The murine LCs also respond more robustly to LH stimulation, with a greater increment in LH-stimulated testosterone production. Collectively, these data suggest that the mouse LC lineage has a delayed onset, and that it has an accelerated pace of maturation compared with the rat LC lineage. Across comparable maturational stages, LCs exhibit species-specific developmental changes in enzyme expression and capacity for androgen production. Our results demonstrate distinct differences in LC differentiation between mice and rats, and provide informative data for assessing reproductive phenotypes of recombinant mouse models.
Authors:
Xiufeng Wu; Ramamani Arumugam; Ningning Zhang; Mary M Lee
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2010-05-07
Journal Detail:
Title:  Reproduction (Cambridge, England)     Volume:  140     ISSN:  1741-7899     ISO Abbreviation:  Reproduction     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2010-06-29     Completed Date:  2010-10-19     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100966036     Medline TA:  Reproduction     Country:  England    
Other Details:
Languages:  eng     Pagination:  113-21     Citation Subset:  IM    
Affiliation:
Pediatric Endocrine Division, Pediatrics and Cell Biology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, Massachusetts 01655, USA.
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MeSH Terms
Descriptor/Qualifier:
Aging / physiology
Androgens / biosynthesis,  metabolism*
Animals
Blotting, Northern
Cell Differentiation / physiology
Cell Separation
Female
Immunohistochemistry
Leydig Cells / drug effects,  metabolism*
Luteinizing Hormone / pharmacology*
Male
Mice
Mice, Transgenic
Pregnancy
RNA, Messenger / biosynthesis,  genetics
Rats
Reverse Transcriptase Polymerase Chain Reaction
Sexual Maturation / physiology*
Steroids / biosynthesis
Stimulation, Chemical
Testis / cytology*,  growth & development*,  metabolism
Grant Support
ID/Acronym/Agency:
DK32520/DK/NIDDK NIH HHS; K02-HD01367/HD/NICHD NIH HHS; R01-HD045773/HD/NICHD NIH HHS; R29-HD36768/HD/NICHD NIH HHS; U54-HD28934/HD/NICHD NIH HHS
Chemical
Reg. No./Substance:
0/Androgens; 0/RNA, Messenger; 0/Steroids; 9002-67-9/Luteinizing Hormone

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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