Literature DB >> 3342444

Evidence for neuroendocrine regulation of preadipocyte proliferation and differentiation.

T G Ramsay1, G J Hausman, R J Martin.   

Abstract

Cells in fetal adipose tissue and cells in vitro are characterized by rapid proliferation. Serum factors have been shown to be important for the rapid proliferation of cells in vitro. The present experiment was performed to determine if neuroendocrine regulatory mechanisms of the fetus can influence the actions of serum factors on preadipocyte proliferation and differentiation in vitro. Sera were obtained from decapitated fetal pigs and intact littermates during gestation. Sera were tested for their effects on primary cultures of preadipocytes and stromal-vascular cells derived from inguinal adipose tissue of young Sprague-Dawley rats. Coverslip cultures were used for histochemical analysis of enzymes after 12 days of incubation with test media. Analysis of growth curves produced from sequential [3H]-thymidine labeling indicated that fetal age influences rates of proliferation. Sera from decapitated fetal pigs specifically reduced the number of proliferating preadipocytes in culture. Sera from decapitated fetal pigs induced a minimum of 50% less differentiation of sn-glycerol-3-phosphate dehydrogenase activity than sera from intact pigs at all fetal ages. Histochemical staining for enzymes of differentiating preadipocytes was also reduced in cultures incubated with sera from decapitated fetal pigs in comparison to sera from intact pigs. The present study has demonstrated that the in vivo effect of decapitation on fetal adipose tissue development is a consequence of alterations in systemic factors present in serum in response to removal of central regulation by the hypothalamic-pituitary axis.

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Year:  1988        PMID: 3342444     DOI: 10.1007/bf00215448

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  24 in total

1.  Effects of fetal decapitation on fetal development, parturition and lactation in pigs.

Authors:  J L Stryker; P J Dziuk
Journal:  J Anim Sci       Date:  1975-02       Impact factor: 3.159

2.  Preparation of collagen substrates for cell attachment: effect of collagen concentration and phosphate buffer.

Authors:  H K Kleinman; E B McGoodwin; S I Rennard; G R Martin
Journal:  Anal Biochem       Date:  1979-04-15       Impact factor: 3.365

3.  Increasing activity of enzymes on pathway of triacylglycerol synthesis during adipose conversion of 3T3 cells.

Authors:  W Kuri-Harcuch; H Green
Journal:  J Biol Chem       Date:  1977-03-25       Impact factor: 5.157

4.  Participation of one isozyme of cytosolic glycerophosphate dehydrogenase in the adipose conversion of 3T3 cells.

Authors:  L S Wise; H Green
Journal:  J Biol Chem       Date:  1979-01-25       Impact factor: 5.157

5.  Adipose conversion of 3T3 cells depends on a serum factor.

Authors:  W Kuri-Harcuch; H Green
Journal:  Proc Natl Acad Sci U S A       Date:  1978-12       Impact factor: 11.205

6.  Techniques for studying adipocytes.

Authors:  G J Hausman
Journal:  Stain Technol       Date:  1981-05

7.  Regulation of DNA synthesis in fat cells and stromal elements from rat adipose tissue.

Authors:  C H Hollenberg; A Vost
Journal:  J Clin Invest       Date:  1969-11       Impact factor: 14.808

8.  Is genetically transmitted obesity due to an adipose tissue defect?

Authors:  C J Meade; M Ashwell; C Sowter
Journal:  Proc R Soc Lond B Biol Sci       Date:  1979-08-31

9.  A quantitative study of human fat transplants in obese nude mice and their lean littermates.

Authors:  C J Meade; M Ashwell
Journal:  Metabolism       Date:  1981-04       Impact factor: 8.694

10.  Adipose tissue development in the fetal pig after decapitation.

Authors:  G J Hausman; D R Campion; J P McNamara; R L Richardson; R J Martin
Journal:  J Anim Sci       Date:  1981-12       Impact factor: 3.159

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