Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1980 Jan 1;84(1):57–65. doi: 10.1083/jcb.84.1.57

Surface structure changes of rat adipocytes during lypolysis stimulated by various lypolysis stimulated by various lypolytic agents

RM Smith, L Jarett
PMCID: PMC2110537  PMID: 6243126

Abstract

A qualitative and quantitative electron microscopic study was performed on rat adipocytes during stimulation of lipolysis by various agents. Scanning electron microscopy of control cells revealed a spherical cell with a textured glycocalyx surface exhibiting small irregular projections. Globular surface evaginations or protrusions measuring 8-18 μM in diameter were seen on cell hemispheres, and there was an average of one protrusion for every two hemispheres examined. Distribution analysis showed that 60 percent of the hemispheres had no protrusions, and 25, 10, and 5 percent of the hemispheres had one, two or three protrusions, respectively. Thin-section and freeze- fracture electron microscopy of the protrusions showed a small triglyceride droplet surrounded by a thin cytoplasmic rim that was continuous with the main cytoplasmic matrix. The glycocalyx coating and plasma membrane extended from the cell surface onto, and over, the protrusion. Scanning microscopy of cells stimulated by lipolytic agents, including epinephrine, adrenocorticotropic hormone, theophylline, and dibutyryl cyclic AMP, revealed a dose-dependent increase in the number of protrusions per cell hemisphere. Maximal concentrations of lipolytic hormones cuase an average 2.5-fold increase in the number of protrusions per hemisphere without changing the average size of the protrusions. Only 40 percent of the stimulated cell hemispheres exhibited no protrusions; over 15 percent of the cells contained three or more; and a number of the protrusions were multilobulate. Insulin prevented the increase in the number of protrusions and the change in distribution caused by the lipolytic hormones but did not prevent the increase caused by theophylline and dibutryl cyclic AMP. The data suggest that the protrusions are a structural feature of the cell and may be related to the lypolytic pathway. These observations may help explain some of the discrepant biochemical data relating to hormonal stimulation of lipolysis.

Full Text

The Full Text of this article is available as a PDF (782.9 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Benjamin W. B., Clayton N. L. Action of insulin and catecholamines on the phosphorylation of proteins associated with the cytosol, membranes, and "fat cake" of rat fat cells. J Biol Chem. 1978 Mar 10;253(5):1700–1709. [PubMed] [Google Scholar]
  2. Carpentier J., Perrelet A., Orci L. Morphological changes of the adipose cell plasma membrane during lipolysis. J Cell Biol. 1977 Jan;72(1):104–117. doi: 10.1083/jcb.72.1.104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Heersche J. N., Fedak S. A., Aurbach G. D. The mode of action of dibutyryl adenosine 3',5'-monophosphate on bone tissue in vitro. J Biol Chem. 1971 Nov 25;246(22):6770–6775. [PubMed] [Google Scholar]
  4. Jarett L., Smith R. M. Electron microscopic demonstration of insulin receptors on adipocyte plasma membranes utilizing a ferritin-insulin conjugate. J Biol Chem. 1974 Nov 10;249(21):7024–7031. [PubMed] [Google Scholar]
  5. Jarett L., Smith R. M. Mode of action of N6-O2'-dibutyryl cyclic 3',5' AMP on fat cell metabolism. Diabetes. 1974 Jan;23(1):29–40. doi: 10.2337/diab.23.1.29. [DOI] [PubMed] [Google Scholar]
  6. Jarett L., Smith R. M. Ultrastructural localization of insulin receptors on adipocytes. Proc Natl Acad Sci U S A. 1975 Sep;72(9):3526–3530. doi: 10.1073/pnas.72.9.3526. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Jarett L., Steiner A. L., Smith R. M., Kipnis D. M. The involvement of cyclic AMP in the hormonal regulation of protein synthesis in rat adipocytes. Endocrinology. 1972 May;90(5):1277–1284. doi: 10.1210/endo-90-5-1277. [DOI] [PubMed] [Google Scholar]
  8. Khoo J. C., Jarett L., Mayer S. E., Steinberg D. Subcellular distribution of and epinephrine-induced changes in hormone-sensitive lipase, phosphorylase, and phosphorylase kinase in rat adipocytes. J Biol Chem. 1972 Aug 10;247(15):4812–4818. [PubMed] [Google Scholar]
  9. Kono T., Robinson F. W., Sarver J. A. Insulin-sensitive phosphodiesterase. Its localization, hormonal stimulation, and oxidative stabilization. J Biol Chem. 1975 Oct 10;250(19):7826–7835. [PubMed] [Google Scholar]
  10. Loten E. G., Sneyd J. G. An effect of insulin on adipose-tissue adenosine 3':5'-cyclic monophosphate phosphodiesterase. Biochem J. 1970 Nov;120(1):187–193. doi: 10.1042/bj1200187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Muller L. L., Jacks T. J. Rapid chemical dehydration of samples for electron microscopic examinations. J Histochem Cytochem. 1975 Feb;23(2):107–110. doi: 10.1177/23.2.1117127. [DOI] [PubMed] [Google Scholar]
  12. Pihl E., Bahr G. F. A new approach to the study of cell organelles with the electron microscope. Exp Cell Res. 1970 Mar;59(3):379–382. doi: 10.1016/0014-4827(70)90644-0. [DOI] [PubMed] [Google Scholar]
  13. RODBELL M. METABOLISM OF ISOLATED FAT CELLS. I. EFFECTS OF HORMONES ON GLUCOSE METABOLISM AND LIPOLYSIS. J Biol Chem. 1964 Feb;239:375–380. [PubMed] [Google Scholar]
  14. Scow R. O., Desnuelle P., Verger R. Lipolysis and lipid movement in a membrane model. Action of lipoprotein lipase. J Biol Chem. 1979 Jul 25;254(14):6456–6463. [PubMed] [Google Scholar]
  15. Slavin B. G. The cytophysiology of mammalian adipose cells. Int Rev Cytol. 1972;33:297–334. doi: 10.1016/s0074-7696(08)61453-9. [DOI] [PubMed] [Google Scholar]
  16. Steinberg D., Huttunen J. K. The role of cyclic AMP in activation of hormone-sensitive lipase of adipose tissue. Adv Cyclic Nucleotide Res. 1972;1:47–62. [PubMed] [Google Scholar]
  17. Steinberg D., Khoo J. C. Hormone-sensitive lipase of adipose tissue. Fed Proc. 1977 Jun;36(7):1986–1990. [PubMed] [Google Scholar]
  18. Wise L. S., Jungas R. L. Evidence for a dual mechanism of lipolysis activation by epinephrine in rat adipose tissue. J Biol Chem. 1978 Apr 25;253(8):2624–2627. [PubMed] [Google Scholar]
  19. Zinder O., Shapiro B. Effect of cell size on epinephrine- and ACTH-induced fatty acid release from isolated fat cells. J Lipid Res. 1971 Jan;12(1):91–95. [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES