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Effect Of Methimazole On ERS Induced ICAM-1?VCAM-1 Expression In Thyroid Cells

Posted on:2020-10-24Degree:MasterType:Thesis
Country:ChinaCandidate:P F LiaoFull Text:PDF
GTID:2404330623955319Subject:Internal medicine
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ObjectiveTo investigate the effects of anti-thyroid drug Methimazole on the expressions of ICAM-1 and VCAM-1 in human normal thyroid cells induced by endoplasmic reticulum stress,and to study the effects of Methimazole on endoplasmic reticulum stress proteins.MethodsUsing T25 cell culture flask cultivate normal thyroid cell line?Nthy-ori-3-1?in37?5%CO2 incubator untill logarithmic growth phase,then transfer cells to six-well plate to cultivate.The cell will be experimental object when they touch each other and fusion degree up to 100%.Thyroid cells were treated with endoplasmic reticulum stress agonist Tunicamycin?TM?and anti-thyroid drug Methimazole?MMI?,and the cell were divided into four groups:Control group 1,Control group 2,Tunicamycin group,Tunicamycin+Methimazole group.Proteins were extracted after intervention,then detected the expression of proteins of ICAM-1,VCAM-1,PERK,IRE1,ATF6 and GRP78 by western blot.Results1.The relative expression levels of ICAM-1 in tunicamycin group,control group 1and control group 2 were 0.457±0.035?0.077±0.015 and 0.113±0.024;The relative expression levels of VCAM-1 in tunicamycin group,control group 1 and control group2 were 0.490±0.116?0.053±0.024 and 0.093±0.034;The relative expression levels of PERK in tunicamycin group and control group 1 and control group 2 were 0.825±0.075?0.090±0.021 and 0.137±0.037;The relative expression levels of IRE1 in tunicamycin group and control group 1 and control group 2 were 0.630±0.085?0.083±0.023 and0.141±0.0361;The relative expression levels of GRP78 in tunicamycin group,control group 1 and control group 2 were 1.700±0.150?0.176±0.540 and 0.222±0.122;Therefore,?1?the expression levels of ICAM-1 and VCAM-1 in tunicamycin group were significantly higher than those in control group 1 and control group 2?p<0.05?,and the expression levels of endoplasmic reticulum stress related proteins?PERK,ATF6,IRE1,GRP78?were also significantly increased?p<0.05?.?2?there was no significant difference in expression of ICAM-1,VCAM-1,PERK,IRE1,ATF6,GRP78 between control group 1 and control group 2?p>0.05?.2.The relative expression levels of ICAM-1 in tunicamycin+methimazole group and tunicamycin group were 0.180±0.017 and 0.387±0.041;The relative expression levels of VCAM-1 in tunicamycin+methimazole group and tunicamycin group were0.160±0.036 and 0.413±0.041;The relative expression levels of PERK in tunicamycin+methimazole group and tunicamycin group were 0.120±0.050 and 0.963±0.073;The relative expression levels of IRE1 in tunicamycin+methimazole group and tunicamycin group were 0.100±0.040 and 0.550±0.029;The relative expression levels of ATF6 in tunicamycin+methimazole group and tunicamycin group were 0.430±0.053 and0.873±0.136;The relative expression levels of GRP78 in tunicamycin+methimazole and tunicamycin group were 0.277±0.058 and 1.773±0.114;Therefore,?1?the expressions of ICAM-1,VCAM-1 in the tunicamycin+methimazole group were significantly lower than those in the tunicamycin group?p<0.05?,and the expressions of endoplasmic reticulum stress related proteins?PERK,ATF6,IRE1,GRP78?in the tunicamycin+methimazole group were also significantly lower than those in the tunicamycin group?p<0.05?.?2?There was no significant difference in expression of ICAM-1,VCAM-1,PERK,ATF6,IRE1,GRP78 between control group 1 and control group 2?p>0.05?.Conclusions1.Endoplasmic reticulum stress induced by Tunicamycin promotes the expression of ICAM-1 and VCAM-1 protein in thyroid cells.2.Methimazole inhibited the expression of ICAM-1 and VCAM-1 protein induced by endoplasmic reticulum stress,as well as the expression of endoplasmic reticulum stress related proteins PERK,IRE1,ATF6 and GRP78.Methimazole can inhibited the expression of ICAM-1 and VCAM-1 proteins by inhibiting the pathway of endoplasmic reticulum stress.
Keywords/Search Tags:Methimazole, ERS, ICAM-1, VCAM-1, Tunicamycin, adhesion molecule
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