Source:http://linkedlifedata.com/resource/pubmed/id/11544564
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2001-9-6
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pubmed:abstractText |
Previous studies have shown that B lymphopoiesis is augmented after androgen withdrawal in male mice. As an analogy to the skeletal system, some effects of androgens on the proliferation of B cells may be mediated via aromatization into estrogens in vivo. The aim of the present study was to assess the effects of androgen withdrawal on B lymphopoiesis in bone marrow of aged male rats sequentially over a period of 9 months, and to correlate the flow-cytometric findings with changes in systemic levels of sex steroids. We first showed that androgen withdrawal is associated with enhanced B lymphopoiesis in bone marrow of 4-month-old male orchiectomized (ORX) rats, and that the changes in the bone marrow B cell compartment in ORX animals can be reversed by testosterone supplementation. In a subsequent, sequential experiment, we found that orchiectomy induced a sustained rise in Thy 1.1+/CD45R+ bone marrow cells committed for the B cell lineage that lasted for several months in 13-month-old aged rats. In a stepwise model of multiple regression analysis using estradiol, free and total testosterone as independent variables, estradiol was the strongest predictor of the percentage of B precursor cells in bone marrow in aged SHAM and ORX rats. Free and total testosterone did not correlate with B lymphopoiesis in aged SHAM rats. The current experiment has clearly shown that androgen withdrawal upregulates the number of B lineage cells over several months in rat bone marrow. Furthermore, our results provide evidence that estradiol may play an important role as a physiological suppressor of B lymphopoiesis in aged male rats.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0018-5043
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
491-8
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pubmed:dateRevised |
2009-2-19
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pubmed:meshHeading |
pubmed-meshheading:11544564-Aging,
pubmed-meshheading:11544564-Androgens,
pubmed-meshheading:11544564-Animals,
pubmed-meshheading:11544564-B-Lymphocytes,
pubmed-meshheading:11544564-Estradiol,
pubmed-meshheading:11544564-Flow Cytometry,
pubmed-meshheading:11544564-Fluorescent Antibody Technique,
pubmed-meshheading:11544564-Hematopoiesis,
pubmed-meshheading:11544564-Hematopoietic Stem Cells,
pubmed-meshheading:11544564-Male,
pubmed-meshheading:11544564-Orchiectomy,
pubmed-meshheading:11544564-Rats,
pubmed-meshheading:11544564-Rats, Inbred F344,
pubmed-meshheading:11544564-Regression Analysis,
pubmed-meshheading:11544564-Testosterone,
pubmed-meshheading:11544564-Up-Regulation
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pubmed:year |
2001
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pubmed:articleTitle |
B lymphopoiesis is upregulated after orchiectomy and is correlated with estradiol but not testosterone serum levels in aged male rats.
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pubmed:affiliation |
Institute of Physiology, Physiological Chemistry and Animal Nutrition, Ludwig Maximilians University, Munich, Germany. R.Erben@lrz.uni-muenchen.de
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pubmed:publicationType |
Journal Article
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