Antibodies against cerebral M1 cholinergic muscarinic receptor from schizophrenic patients:: Molecular interaction

被引:46
作者
Borda, T
Rivera, RP
Joensen, L
Gomez, RM
Sterin-Borda, L
机构
[1] Univ Buenos Aires, Fac Odontol, Catedra Farmacol, Sch Med & Dent,Dept Pharmacol, Buenos Aires, DF, Argentina
[2] Argentine Natl Res Council, Buenos Aires, DF, Argentina
关键词
D O I
10.4049/jimmunol.168.7.3667
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We demonstrated the presence of circulating Abs from schizophrenic patients able to interact with cerebral frontal cortex-activating muscarinic acetylcholine receptors (mAChR). Sera and purified IgG from 21 paranoid schizophrenic and 25 age-matched normal subjects were studied by indirect immunofluorescence, flow cytometry, immunoblotting, dot blot, ELISA, and radioligand competition assays. Rat cerebral frontal cortex membranes and/or a synthetic peptide, with an amino acid sequence identical with that of human M-1 mAChR, were used as Ags. By indirect immunofluorescence and flow cytometry procedures, we proved that serum-purified IgG fraction from schizophrenic patients reacted to neural cell surfaces from rat cerebral frontal cortex. The same Abs were able to inhibit the binding of the specific M-1 mAChR radioligand [H-3]pirenzepine. Immunoblotting experiments showed that IgG from schizophrenic patients revealed a band with a molecular mass coincident to that labeled by an anti-M-1 mAChR Ab. Using synthetic peptide for dot blot and ELISA, we demonstrated that these Abs reacted against the second extracellular loop of human cerebral M-1 mAChR. Also, the corresponding affinity-purified antipeptide Ab displayed an agonistic-like activity associated to specific receptor activation, increasing cyclic GMP production and inositol phosphate accumulation, and protein kinase C translocation. This paper gave support to the participation of an autoimmune process in schizophrenia.
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页码:3667 / 3674
页数:8
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