Zou J, Jiang S, Zhou Y
Bethune International Peace Hospital, Shijiazhuang 050082.
Zhonghua Er Bi Yan Hou Ke Za Zhi. 1998 Oct;33(5):282-4.
To investigate the association between bacteria antigen and inner ear antigen and effects of stress on the expression spectrum and level of the antigen bearing hsp70 related epitope.
Use monoclonal antibody against mammiferous hsp70 to recognize the related antigens of Bacillus pyocyaneus, Bacillus proteus, Bacillus coli, Staphylococcus aureus and Klebsiella pneumoniae with modified western blotting. The expression level of hsp70 in unstressed guinea pig inner ear was tested. An animal model of middle ear acute infection by Klebsiella pneumoniae was established. The dynamic changes of mammiferous hsp70 epitope related proteins were tested with modified western blotting.
All the bacteria antigens recognized by anti-mammiferous hsp70 antibody were not of the hsp70 family and the expression level of hsp70 in normal guinea pig was extraordinarily low. Klebsiella pneumoniae expressed 70,000 dalton and 17,000 dalton hsp after its invasion into guinea pig middle ear. 70,000 dalton antigen expressed most intensely at 3rd day of invasion and then fell. 17,000 dalton antigen was expressed most intensely at 5th day of invasion and then fell. The expression of 70,000 dalton hsp was much weaker than 31,000 dalton hsp at acute periods of middle ear infection.
The elevated expression of hsp both in bacteria and inner ear during middle ear acute infection provides material base for immune impairment on inner ear induced by bacterial infection. The low molecular weight hsp may be involved in the inner ear autoimmune impairment.
探讨细菌抗原与内耳抗原之间的关联以及应激对携带热休克蛋白70(hsp70)相关表位的抗原表达谱和水平的影响。
用抗哺乳动物hsp70单克隆抗体,采用改良的蛋白质印迹法识别铜绿假单胞菌、变形杆菌、大肠杆菌、金黄色葡萄球菌和肺炎克雷伯菌的相关抗原。检测未受应激的豚鼠内耳中hsp70的表达水平。建立肺炎克雷伯菌中耳急性感染动物模型。采用改良的蛋白质印迹法检测哺乳动物hsp70表位相关蛋白的动态变化。
抗哺乳动物hsp70抗体识别的所有细菌抗原均不属于hsp70家族,正常豚鼠中hsp70的表达水平极低。肺炎克雷伯菌侵入豚鼠中耳后表达70000道尔顿和17000道尔顿的热休克蛋白。70000道尔顿抗原在侵入后第3天表达最强,随后下降。17000道尔顿抗原在侵入后第5天表达最强,随后下降。在中耳感染急性期,70000道尔顿热休克蛋白的表达比31000道尔顿热休克蛋白弱得多。
中耳急性感染期间细菌和内耳中热休克蛋白表达升高为细菌感染诱导内耳免疫损伤提供了物质基础。低分子量热休克蛋白可能参与内耳自身免疫损伤。