spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by LEWIS, J. A.
Right arrow Articles by TATA, J. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by LEWIS, J. A.
Right arrow Articles by TATA, J. R.

Journal of Cell Science, Vol 13, 447-459, Copyright © 1973 by Company of Biologists

Submitted on January 30, 1973

A Rapidly Sedimenting Fraction of Rat Liver Endoplasmic Reticulum

J. A. LEWIS 1 and J. R. TATA 1

1 National Institute for Medical Research, Mill Hill, London, NW7 1AA, U.K

Balance-sheet experiments carried out to account for the distribution of endoplasmic reticulum fragments during subcellular fractionation of rat liver showed that a large proportion of these fragments are present in the pellets of low-speed centrifugation. Using glucose-6-phosphatase and RNA as markers we found that approximately 50% of the fragments of endoplasmic reticulum sedimented in the pellet of a 640-g centrifugation, 10% in that of a 6000-g centrifugation and 35% in the pellet of a 105000-g centrifugation. Starvation of the animals before use did not alter this distribution, nor did the use of more vigorous homogenization conditions. We have developed a procedure for removing nuclei and erythrocytes from the material sedimenting at 640g to give a fraction (rapidly sedimenting ER fraction or RS-ER) similar to the standard microsomal preparation. Centrifugation of this RS-ER fraction over 1.3 M sucrose yields subfractions of high and low RNA content analogous to the rough and smooth microsomal fractions. Electron-microscopic studies showed that, whereas the rough microsomal fraction consisted of ribosome-studded vesicles of varying size and content density, the rough RS-ER fraction contained a mixture of mitochondria and double lamellar membranes with ribosomes attached. These double lamellar membranes closely resemble the endoplasmic reticulum of intact rat liver. The double lamellar membranes are frequently observed grouped in stacks and in close association with the mitochondria. The significance of the association between endoplasmic reticulum and mitochondria of the RS-ER fraction and the relation between it and the standard microsomal preparation are discussed.

Submitted on January 30, 1973




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
A. Pottekat and A. K. Menon
Subcellular Localization and Targeting of N-Acetylglucosaminyl Phosphatidylinositol De-N-acetylase, the Second Enzyme in the Glycosylphosphatidylinositol Biosynthetic Pathway
J. Biol. Chem., April 16, 2004; 279(16): 15743 - 15751.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
H.-J. Wang, G. Guay, L. Pogan, R. Sauve, and I. R. Nabi
Calcium Regulates the Association between Mitochondria and a Smooth Subdomain of the Endoplasmic Reticulum
J. Cell Biol., September 18, 2000; 150(6): 1489 - 1498.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1973