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 Vaux, D. J.
Right arrow Articles by Gordon, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vaux, D. J.
Right arrow Articles by Gordon, S.

Journal of Cell Science, Vol 77, Issue 1 109-127, Copyright © 1985 by Company of Biologists


JOURNAL ARTICLES

Intracellular antigens associated with the cytoplasmic surface of phagolysosomes

DJ Vaux and S Gordon

Monoclonal antibodies were prepared to study the cytoplasmic face of latex phagolysosomes isolated from thioglycollate-elicited mouse peritoneal macrophages. Phagolysosomes obtained by sucrose flotation contained latent beta-glucuronidase activity and tightly associated cellular proteins and glycoproteins. Fluorescence-activated cell sorter analysis, scanning and transmission electron microscopy showed that the particle preparation contained greater than 98% monomers and dimers, invested with a smooth layer of membrane and minimally contaminated with cytoplasmic adhesions. Sera for immunized rats bound preferentially to isolated phagolysosomes rather than intact cells and monoclonal antibodies PL-1 and PL-4 were isolated on this basis. Indirect fluorescent, radio- and peroxidase immunobinding assays with intact and methanol-permeabilized cells confirmed that antigens PL-1 and PL-4 were exclusively intracellular and that well-washed phagolysosomes bound both antibodies. These antigens were found in a variety of cells from several species and in macrophages not fed latex. Although the PL-1 antigen could not be immunoprecipitated, intracellular staining was characteristic of intermediate filament distribution, that is, it was in the form of a fine intersecting network, which collapsed, reversibly, in a rim round the nucleus upon treatment with colcemid. The staining pattern was undetectable in cells 1 h after adherence to a substratum, but gradually appeared after 6-12 h. The PL-4 antibody has been shown elsewhere to define a Ca2+-binding protein of approximately 20 000 molecular weight, which is phosphorylated during phagocytosis. This antibody stained stress fibres and revealed a widespread punctate distribution of antigen within cells at all stages after adhesion. The nature of the association between these intracellular antigens and phagolysosomes and their possible role in phagocytosis are not known.


This article has been cited by other articles:


Home page
JCBHome page
C. P. Maske, M. S. Hollinshead, N. C. Higbee, M. O. Bergo, S. G. Young, and D. J. Vaux
A carboxyl-terminal interaction of lamin B1 is dependent on the CAAX endoprotease Rce1 and carboxymethylation
J. Cell Biol., September 29, 2003; 162(7): 1223 - 1232.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1985