Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1963 Sep 1;18(3):503–513. doi: 10.1083/jcb.18.3.503

PHOTOMETRIC EVIDENCE FOR THE OSMOTIC BEHAVIOR OF RAT LIVER MICROSOMES

Henry Tedeschi 1, Joseph M James 1, William Anthony 1
PMCID: PMC2106319  PMID: 14064105

Abstract

Electron microscope observations are consistent with the interpretation that the elements of the endoplasmic reticulum are osmotically active in situ as well as after isolation. More recently, it has been reported that microsomal suspensions equilibrate almost completely with added C14-sucrose and that no osmotic behavior is evident from photometric data. These findings were considered at variance with the electron microscope data. However, equilibration with added label simply attests to a relatively high permeability, and, in addition, the photometric data need not be critical. Osmotic volume changes, measured photometrically, may be masked by concomitant events (e.g., changes in the refractive index of the test solutions at varying osmotic pressures, breakdown of the particles, and agglutination). For these reasons the photometric experiments were repeated. In this work, the reciprocal of optical density of microsomal suspensions was found to vary linearly with the reciprocal of concentration of the medium at constant refractive index. These changes probably correspond to osmotic volume changes, since the effect was found to be (a) independent of substance used and (b) osmotically reversible. The transmission of the suspension was found to vary with the refractive index of the medium, the concentration of particles, and the wavelength of incident light, according to relationships that are similar to or identical with those obtained for mitochondrial suspensions.

Full Text

The Full Text of this article is available as a PDF (746.8 KB).

Selected References

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

  1. ALLFREY V. G., MEUDT R., HOPKINS J. W., MIRSKY A. E. Sodium-dependent "transport" reactions in the cell nucleus and their role in protein and nucleic acid synthesis. Proc Natl Acad Sci U S A. 1961 Jul 15;47:907–932. doi: 10.1073/pnas.47.7.907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BARER R., ROSS K. F. A., TKACZYK S. Refractometry of living cells. Nature. 1953 Apr 25;171(4356):720–724. doi: 10.1038/171720a0. [DOI] [PubMed] [Google Scholar]
  3. BRIERLEY G. P., BACHMANN E., GREEN D. E. Active transport of inorganic phosphate and magnesium ions by beef heart mitochondria. Proc Natl Acad Sci U S A. 1962 Nov 15;48:1928–1935. doi: 10.1073/pnas.48.11.1928. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. GREEN D. E., HATEFI Y. The mitochondrion and biochemical machines. Science. 1961 Jan 6;133(3445):13–19. doi: 10.1126/science.133.3445.13. [DOI] [PubMed] [Google Scholar]
  5. HASSELBACH W., MAKINOSE M. [The calcium pump of the "relaxing granules" of muscle and its dependence on ATP-splitting]. Biochem Z. 1961;333:518–528. [PubMed] [Google Scholar]
  6. PALADE G. E., SIEKEVITZ P. Liver microsomes; an integrated morphological and biochemical study. J Biophys Biochem Cytol. 1956 Mar 25;2(2):171–200. doi: 10.1083/jcb.2.2.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. PAULY H., PACKER L. The relationship of internal conductance and membrane capacity to mitochondrial volume. J Biophys Biochem Cytol. 1960 Jul;7:603–612. doi: 10.1083/jcb.7.4.603. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. SHARE L., HANSROTE R. W. Permeability of rat liver microsomes to sucrose and carboxypolyglucose in vitro. J Biophys Biochem Cytol. 1960 Apr;7:239–242. doi: 10.1083/jcb.7.2.239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. SLAUTTERBACK D. B. Electron microscopic studies of small cytoplasmic particles (microsomes). Exp Cell Res. 1953 Sep;5(1):173–186. doi: 10.1016/0014-4827(53)90102-5. [DOI] [PubMed] [Google Scholar]
  10. TEDESCHI H., HARRIS D. L. Some observations on the photometric estimation of mitochondrial volume. Biochim Biophys Acta. 1958 May;28(2):392–402. doi: 10.1016/0006-3002(58)90487-6. [DOI] [PubMed] [Google Scholar]
  11. TEDESCHI H., HARRIS D. L. The osmotic behavior and permeability to non-electrolytes of mitochondria. Arch Biochem Biophys. 1955 Sep;58(1):52–67. doi: 10.1016/0003-9861(55)90092-8. [DOI] [PubMed] [Google Scholar]
  12. TEDESCHI H. The structure of the mitochondrial membrane: inferences from permeability properties. J Biophys Biochem Cytol. 1959 Oct;6:241–252. doi: 10.1083/jcb.6.2.241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. WEISS J. M. The ergastoplasm; its fine structure and relation to protein synthesis as studied with the electron microscope in the pancreas of the Swiss albino mouse. J Exp Med. 1953 Dec;98(6):607–618. doi: 10.1084/jem.98.6.607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. von EULER U., LISHAJKO F. Noradrenaline release from isolated nerve granules. Acta Physiol Scand. 1961 Feb-Mar;51:193–203. doi: 10.1111/j.1748-1716.1961.tb02145.x. [DOI] [PubMed] [Google Scholar]

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

RESOURCES