JCB logo
Keystone Symposia 2008 Scientific Conferences
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published 28 February 2005. doi:10.1083/jcb1685fta2
The Rockefeller University Press, 0021-9525 $8.00
JCB, Volume 168, Number 5, 676-677
This Article
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wells, W. A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Wells, W. A.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

From the Archive

Autophagy unveiled

In cell biology research it seems that building gets more attention than destruction: work on the cell cycle leapt ahead while apoptosis research was in its infancy, and protein synthesis pathways were well established when autophagy was, for most researchers, a word that drew blank stares.
A double membrane surrounds organelles such as mitochondria (A) during autophagy.

PORTER

Thus the molecular description of autophagy is a relatively recent phenomenon (Klionsky and Emr, 2000). But the morphology came early. Autophagy is the destructive process in which a double membrane envelops cytoplasm and organelles before targeting them to lysosomes for destruction. It was first spotted in differentiating kidney cells as they redirected their metabolic energies (Clark, 1957).

A robust model was established by Ashford and Porter (1962), who spotted autophagy when glucagon was perfused into rat livers. Glucagon is made in response to low blood sugar levels, so autophagy may be the cell's way of scaling back operations in hard times. In the words of Ashford and Porter (1962), the hydrolysis may be "providing the protoplast with breakdown products for use in a reoriented physiology," with the membrane "shield[ing] the rest of the cell from the general spread of the degradative process."

The word autophagy crept into the literature in the 1960s (Deter et al., 1967) as it became clear that the process intersected with but was distinct from other forms of lysosomal degradation. The endoplasmic reticulum was proposed as the source of the autophagic membranes (Dunn, 1990), although uncertainties about this and other details of autophagy remain. {fta_end}

Ashford, T.P., and K.R. Porter. 1962. J. Cell Biol. 12:198–202.[Free Full Text]

Clark, S.L. 1957. J. Biophys. Biochem. Cytol. 3:349–361.[Abstract/Free Full Text]

Deter, R.L., et al. 1967. J. Cell Biol. 35:C11–C16.[Free Full Text]

Dunn, W.A. 1990. J. Cell Biol. 110:1923–1933.[Abstract/Free Full Text]

Klionsky, D.J., and S.D. Emr. 2000. Science. 290:1717–1721.[Abstract/Free Full Text]



William A. Wells

wellsw{at}rockefeller.edu


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?



This Article
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wells, W. A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Wells, W. A.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?


  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents