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作 者:刘颖新[1] 白秀峰[1] 赖向东[2] 郭海英[1] 罗燕[1] 余裕[1] 连小华[1]
机构地区:[1]第三军医大学基础医学部细胞生物学教研室,重庆400038 [2]第三军医大学西南医院肝胆外科,重庆400038
出 处:《第三军医大学学报》2016年第3期238-244,共7页Journal of Third Military Medical University
基 金:国家自然科学基金面上项目(81171515);重庆市自然科学基金青年科研基金(CSTC2013jcyjA10021)~~
摘 要:目的初步探讨Gsdermin A3(Gsdma3)基因对Krt6b基因表达的影响。方法通过组织切片的免疫荧光观察、RT-PCR、Q-PCR、Western blot等方法检测毛囊生长期[出生后8 d(P8d)]、毛囊退化期(P16d)、毛囊静止期(P25d)的Gsdma3基因突变鼠(AE鼠)和野生型鼠(WT鼠)背部皮肤Krt6b基因的表达情况。利用免疫荧光进一步观察注射有Gsdma3和RFP腺病毒的Gsdma3基因突变鼠和野生型鼠的Krt6b基因的表达情况。结果 Gsdma3基因突变鼠的Krt6b基因表达量在各个时相点均高于野生型鼠(P<0.05)。其中,在出生后16 d Krt6b基因表达量达到最高,而在出生后25 d降至最低。对Gsdma3基因突变鼠进行基因回补后,免疫荧光、实时定量PCR及Western blot检测结果显示Krt6b基因表达减弱。同时,对野生型鼠过表达Gsdma3基因后,免疫荧光、实时定量PCR及Western blot结果显示Krt6b基因表达量降低。结论小鼠皮肤角质形成细胞中,Krt6b基因的表达受Gsdma3基因抑制。Objective To determine the effect of Gsdermin A3( Gsdma3) on the expression of Krt6 b.Methods Q-PCR,RT-PCR,Western blotting and immunohistochemical staining were used to detect the expression of Krt6 b at mRNA and protein levels in Gsdma3 mutant mice( AE) and C57 BL /6J wild-type mice( WT) at 3 time points in mouse hair follicle cycle( anagen: 8 d postnatally,catagen: 16 d postnatally,telogen: 25 d postnatally). Immunofluorescence assay was also used to determine the effect of the adenoviruses carrying Gsdma3 gene( Ad Gsdma3) or control gene( AdRFP) on the expression of Krt6 b in AE and WT mice. Results The expression level of Krt6 b was obviously higher in Gsdma3 mutant mice than WT mice( P〈0. 05). At P16,the expression of Krt6 b reached the highest level,while on P25 it reduced to the lowest level. Immunofluorescence assay,real-time PCR and Western blotting showed that the expression of Krt6 b was decreased in Gsdma3 mutant mice after Gsdma3 expression rescue. Meanwhile,immunofluorescence assay showed that the expression of Krt6 b was also decreased in WT mice with Gsdma3 over-expression.Conclusion Gsdma3 inhibits the expression of Krt6 b in mouse keratinocytes.
关 键 词:Gsdermin A3基因 Krt6b基因 角质形成细胞 小鼠
分 类 号:R322.991[医药卫生—人体解剖和组织胚胎学] R329.25[医药卫生—基础医学]
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