Autoantibodies against nuclear pore membrane protein GP210: Evidence for molecular mimicry in primary biliary cirrhosis? . Department of Medicine and Brookdate Center for Molacular Biology, Mount Sinai School of Medicine, New York, NY

Hepatology ◽  
1993 ◽  
Vol 18 (4) ◽  
pp. A109
1980 ◽  
Vol 4 (11) ◽  
pp. 184-184

The Association for Research in Nervous and Mental Disease will hold its annual meeting on 5 and 6 December, 1980 at the Grand Hyatt Hotel in New York City. The meeting will be devoted to the ‘Genetics of Neurological and Psychiatric Disorders’. Information: Secretary-Treasurer of the ARNMD, Bernard Cohen, Mount Sinai School of Medicine, l Gustave Levy Place, NY 10029, USA.


1990 ◽  
Vol 172 (3) ◽  
pp. 961-967 ◽  
Author(s):  
J C Courvalin ◽  
K Lassoued ◽  
H J Worman ◽  
G Blobel

We have identified autoantibodies from two patients with primary biliary cirrhosis (PBC) that recognize the nuclear envelope of mammalian cells on indirect immunofluorescence microscopy. These antibodies bind to a 58-kD integral membrane protein (p58) of the turkey erythrocyte nuclear envelope, which has been previously identified as a membrane receptor for lamin B (Worman, H. J., J. Yuan, G. Blobel, and S. D. Georgatos. 1988. Proc. Natl. Acad. Sci. USA. 85:8531). The antibodies also bind to a 61-kD integral membrane protein (p61) of the rat liver nuclear envelope. Affinity-purified antibodies eluted from turkey p58 bind to rat p61, showing that the two proteins share an epitope(s) and that p61 is likely the rat liver lamin B receptor. In human nuclear envelopes, the antigen recognized has an apparent molecular mass close to that of avian protein. These findings, along with the previous discovery of autoantibodies against an integral membrane glycoprotein (gp210) of the nuclear pore membrane in patients with PBC, suggest that antibodies against integral membrane proteins of the nuclear envelope are characteristic of a subset of patients with PBC.


Sign in / Sign up

Export Citation Format

Share Document