Document Detail

Translocation of apolipoprotein B across the endoplasmic reticulum is blocked in a nonhepatic cell line.
MedLine Citation:
PMID:  1409618     Owner:  NLM     Status:  MEDLINE    
To explore the process of lipoprotein assembly, plasmids encoding truncated forms of apolipoprotein B (apoB) were transfected into Chinese hamster ovary (CHO) fibroblasts. (One, encoding apoB53, the N-terminal 53% of apoB100, can direct the assembly and secretion of lipoproteins when expressed in hepatoma cells, while the other, encoding the shorter apoB15, does not direct lipoprotein assembly.) Expression of apoB15 in CHO cells resulted in the accumulation of apoB15 protein in both medium and cells. In contrast, apoB was not detectable in medium or within CHO cells transfected with the plasmid encoding apoB53, despite the expression of apoB53 mRNA. ApoB53 did accumulate within transfected cells incubated with the thiol protease inhibitor N-acetylleucylleucylnorleucinal (ALLN), suggesting that it is synthesized but completely degraded in the absence of the inhibitor. ApoB53 was not secreted despite its presence within ALLN-treated cells. Essentially all the apoB53 that accumulated in microsomes from ALLN-treated cells was associated with the membrane and was susceptible to degradation by exogenous trypsin, indicating exposure on the cytoplasmic face of the membrane. Thus, translocation of apoB53 across the endoplasmic reticulum membrane is blocked. However, the apoB53 bound to concanavalin A, suggesting that it is glycosylated and therefore partly exposed to the lumen as well. ApoB requires a unique process, not expressed in CHO fibroblasts, for its complete translocation and entrance into the secretory pathway. This process might account for the inability of abetalipoproteinemic patients to secrete apoB.
R N Thrift; J Drisko; S Dueland; J D Trawick; R A Davis
Related Documents :
11267978 - Suppression of proline-directed protein kinase f(a) systemically inhibits the growth of...
22342628 - β-carboline alkaloids from the leaves of trigonostemon lii y.t. chang.
10900408 - Recombinant cell bioassays for endocrine disruptors: development of a stably transfecte...
21781778 - Induction of estradiol 2-hydroxylase activity in mcf-7 human breast cancer cells by pes...
10227388 - Cell surface colligin/hsp47 associates with tetraspanin protein cd9 in epidermoid carci...
9576828 - Spontaneous transdifferentiation of quail pigmented epithelial cell is accompanied by a...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Proceedings of the National Academy of Sciences of the United States of America     Volume:  89     ISSN:  0027-8424     ISO Abbreviation:  Proc. Natl. Acad. Sci. U.S.A.     Publication Date:  1992 Oct 
Date Detail:
Created Date:  1992-11-10     Completed Date:  1992-11-10     Revised Date:  2010-09-07    
Medline Journal Info:
Nlm Unique ID:  7505876     Medline TA:  Proc Natl Acad Sci U S A     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  9161-5     Citation Subset:  IM    
Atherosclerosis Research Center, University of Colorado Health Sciences Center, Denver 80262.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Apolipoproteins B / genetics*,  isolation & purification,  metabolism*
Blotting, Western
CHO Cells
Concanavalin A / metabolism
Electrophoresis, Polyacrylamide Gel
Endoplasmic Reticulum / metabolism*
Liver / metabolism
Microsomes / metabolism
Protein Processing, Post-Translational*
RNA, Messenger / genetics,  isolation & purification,  metabolism
Grant Support
Reg. No./Substance:
0/Apolipoproteins B; 0/RNA, Messenger; 11028-71-0/Concanavalin A

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Coat protein gene duplication in a filamentous RNA virus of plants.
Next Document:  Uncoupling gene activity from chromatin structure: promoter mutations can inactivate transcription o...