|
|
||||||||
J. Biol. Chem., Vol. 258, Issue 1, 20-23, Jan, 1983
RR Aksamit, PS Backlund Jr and GL Cantoni
It has been shown earlier that 3-deazaadenosine but not 3-
deazaaristeromycin inhibits chemotaxis of RAW264 cells (Aksamit, R.R.,
Falk, W., and Cantoni, G.L. (1982) J. Biol. Chem. 257, 621-625). We show
here in RAW264 cells that (a) the incorporation of the methyl group of
methionine into phosphatidylcholine is inhibited approximately 90% by both
3-deazaadenosine and 3-deazaaristeromycin, (b) 3- deazaadenosine but not
3-deazaaristeromycin inhibits the synthesis of specific proteins, and (c)
3'-deoxyadenosine and erythro-9-(2-hydroxy-3- nonyl)-adenine in the
presence of adenosine and homocysteine inhibit chemotaxis and the synthesis
of specific proteins. Inhibition of the synthesis of specific proteins can
be observed only after the solubilized cellular proteins are separated by
two-dimensional polyacrylamide gel electrophoresis, since the adenosine
analogs do not significantly affect total protein synthesis. When total
protein synthesis is inhibited by incubation of the cells with
cycloheximide, puromycin, or actinomycin D, chemotaxis is correspondingly
inhibited. The results suggest that the continuous synthesis of one or more
cellular proteins is required for chemotaxis by RAW264 cells.
Chemotaxis and the synthesis of specific proteins are inhibited by 3- deazaadenosine and other adenosine analogs in a mouse macrophage cell line
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
S. Shu, D. C. Mahadeo, X. Liu, W. Liu, C. A. Parent, and E. D. Korn S-adenosylhomocysteine hydrolase is localized at the front of chemotaxing cells, suggesting a role for transmethylation during migration PNAS, December 26, 2006; 103(52): 19788 - 19793. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Walker, A. C. Langheinrich, E. Dennhauser, R. M. Bohle, T. Dreyer, J. Kreuzer, H. Tillmanns, R. C. Braun-Dullaeus, and W. Haberbosch 3-Deazaadenosine Prevents Adhesion Molecule Expression and Atherosclerotic Lesion Formation in the Aortas of C57BL/6J Mice Arterioscler. Thromb. Vasc. Biol., November 1, 1999; 19(11): 2673 - 2679. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. S. Backlund Jr. Post-translational Processing of RhoA. CARBOXYL METHYLATION OF THE CARBOXYL-TERMINAL PRENYLCYSTEINE INCREASES THE HALF-LIFE OF RhoA J. Biol. Chem., December 26, 1997; 272(52): 33175 - 33180. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Molecular and Cellular Proteomics |
| Journal of Lipid Research | ASBMB Today |