Cardiac expression of 52 beta, an alternative transcript of the congenital heart block-associated 52-kd SS-A/Ro autoantigen, is maximal during fetal development

被引:49
作者
Buyon, JP
Tseng, CE
DiDonato, F
Rashbaum, W
Morris, A
Chan, EKL
机构
[1] NYU, SCH MED, NEW YORK, NY USA
[2] BETH ISRAEL MED CTR, NEW YORK, NY 10003 USA
[3] SCRIPPS RES INST, LA JOLLA, CA USA
来源
ARTHRITIS AND RHEUMATISM | 1997年 / 40卷 / 04期
关键词
D O I
10.1002/art.1780400410
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Congenital heart block (CHB), associated with antibodies to SS-A/Ro and SS-B/La, is most often detected between 18 and 24 weeks of gestation, yet the maternal heart is unaffected, We recently described an alternatively spliced 52-kd SS-A/Ro messenger RNA (mRNA) derived from the skipping of exon 4 which encodes a smaller protein, 52 beta (MW 45 kd), recognized by CHB maternal antisera, This study was designed to identify whether cardiac expression of 52 beta and full-length 52 alpha relates to the development of CHB. Methods. Reverse transcriptase-polymerase chain reaction was performed using primers flanking exon 4 and mRNA from 22 human fetal hearts (age 11-25 weeks) and 3 adult hearts, The brain, kidney, liver, lung, and spleen were similarly evaluated in a 15-week, an 18-week, and a 24-week fetus. Results. Expression of 52 beta was greatest and 52 alpha lowest between 14 and 16 weeks of gestation, In fetal hearts ages 22-25 weeks and adult heart, the 52 beta transcript was markedly diminished and 52 alpha clearly dominated. The 52 beta mRNA was observed in a 15-week brain, kidney, lung, and spleen; however, its expression relative to 52 alpha was greatest in the heart. Conclusion. Since expression of the alternative product 52 beta is maximal at the time of cardiac ontogeny when maternal antibodies gain access to the fetal circulation, just prior to the clinical detection of bradyarrhythmia, a role for 52 beta in the development of CHB is implicated, Although other fetal tissues express 52 beta, there may be differences in accessibility of antigen or regenerative capacities.
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页码:655 / 660
页数:6
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