北京大学学报(医学版) ›› 2017, Vol. 49 ›› Issue (6): 948-953. doi: 10.3969/j.issn.1671-167X.2017.06.003

• 论著 • 上一篇    下一篇

免疫球蛋白A在人肾小球系膜细胞中的合成与分泌

邓会1,马骏凡2,景子洋1,梁耀先1,阿拉塔1,刘洋2,邱晓彦2△,王悦1△   

  1. (1. 北京大学第三医院肾内科,北京100191; 2. 北京大学基础医学院免疫学系,北京100191)
  • 出版日期:2017-12-18 发布日期:2017-12-18
  • 通讯作者: 邱晓彦,王悦 E-mail: bjwangyue@sina.com, qiuxy2014@126.com

Primary investigation of immunoglobulin A synthesis and secretion in human mesangial cells

DENG Hui1, MA Jun-fan2, JING Zi-yang1, LIANG Yao-xian1, A La-ta1, LIU Yang2, QIU Xiao-yan2△, WANG Yue1△   

  1. (1. Department of Nephrology, Peking University Third Hospital, Beijing 100191, China; 2. Department of Immunology, Peking University School of Basic Medical Sciences, Beijing 100191, China)
  • Online:2017-12-18 Published:2017-12-18
  • Contact: QIU Xiao-yan, WANG Yue E-mail: bjwangyue@sina.com, qiuxy2014@126.com

摘要: 目的:探讨人肾小球系膜细胞(human mesangial cells,HMCs)中是否表达免疫球蛋白A(immunoglobulin A,IgA)。方法:培养人HMCs细胞系,以免疫荧光染色检测Ig α、Ig κ、Ig λ在系膜细胞中的表达;以反转录聚合酶链式反应(reverse transcription polymerase chain reaction, RT-PCR)和DNA测序检测HMCs中Ig α、Ig κ、Ig λ恒定区转录本表达;以Western blot方法检测细胞裂解液及培养上清液中Ig α、Ig κ、Ig λ蛋白水平表达;以jacalin为配体的亲和层析纯化上清液蛋白质,以蛋白质谱检测纯化的蛋白氨基酸序列。结果:免疫荧光染色检测到HMCs细胞浆Ig α、 Ig κ、 Ig λ的阳性表达;RT-PCR检测到细胞内Ig α1、Ig α2重链、Ig κ轻链、Ig λ轻链恒定区转录本表达,且其核苷酸序列与美国国立生物技术信息中心(National Center of Biotechnology Information, NCBI)数据库相应的mRNA序列比对,同源性分别达到99%、97%、98%和97%;Western blot检测到细胞内Ig α1、Ig α2和Ig λ蛋白水平的表达,Ig κ目前检测为阴性;细胞上清液中可见完整IgA分子表达;以jacallin为配体亲和层析纯化的培养上清液中的IgA,蛋白质谱测序所得的氨基酸片段序列与NCBI数据库比对,显示HMCs分泌的蛋白质与B细胞表达的Ig α1恒定区52~104之间53个氨基酸、154~221之间68个氨基酸、以及276~327之间52个氨基酸的序列完全相同,与Ig α2重链恒定区52~113之间62个氨基酸、151~204之间54个氨基酸、以及251~314之间64个氨基酸的序列完全相同,提示系膜细胞可以将合成的IgA分泌到胞外。结论:HMCs可能合成并分泌IgA。

关键词: 人肾小球系膜细胞, 免疫球蛋白A, 蛋白质谱, DNA测序

Abstract: Objective: To investigate the expression of immunoglobulin A (IgA) in human mesangial cells (HMCs). Methods: The HMCs were cultured. The subcellular location of IgA was detected by immunofluorescence staining; the transcripts of Ig α,Ig κ and Ig λ constant region were detected by reverse transcriptionpolymerase chain reaction (RT-PCR) and further analyzed by DNA sequencing. The expressions of Ig α and Ig λ were detected at transcription level by Western blot after the cytoplasmic protein extraction. The culture supernatant was collected to explore whether IgA could be secreted out of the cell and the protein was further analyzed by mass spectrometry after being purified by affinity chromato-graphy with jacalin-sepharose. The results of DNA sequencing and mass spectrometry were aligned with the mRNA and amino acid sequences in the National Center of Biotechnology Information (NCBI) database. Results: By immunofluorescence staining, we detected the presence of IgA heavy chain Ig α, light chain, both Ig κ and Ig λ in expressions of transcripts of Ig α1, Ig α2, Ig κ and Ig λ in the HMCs and the alignment of the sequences of the RT-PCR products with those of the Ig Cα1, Ig Cα2, Ig κ and Ig λ mRNA in the NCBI database exhibited that the similarities were 99%, 97%, 98% and 97%, respectively. Western blot showed Ig α and Ig λ expressions in the cell lysate and secretion of Ig α1 and Ig α2 heavy chains in cell culture supernatant. To further explore the protein that secreted into the supernatant, after supernatant affinity chromatography with jacalin-sepharose, the proteins were separated by sodium dodecyl sulfonate-polyacrylamide gel electrophoresis (SDS-PAGE) and the band approximating to 65 000 was cut and sent to mass spectrometry. The results were aligned with the amino acid sequences of Ig α1 and Ig α2 constant region in NCBI database, showing that amino acids between No.52 and No.104, amino acids between No.154 and No.221, amino acids between No.276 and No.327 from Ig Cα1 and amino acids between No.52 and No.113, amino acids between No.151 and No.204, amino acids between No.251 and No.314 from Ig Cα2 were the same with those derived from B cells. Conclusion: Our fin-dings suggested that HMCs could synthesize and secret IgA.

Key words: Human mesangial cell, Immunoglobulin A, Mass spectrometry, DNA sequencing

中图分类号: 

  • R692.6
[1] 张军军, 于峰, 徐丽霞, 张颖, 赵明辉. 糖基化缺陷的血清IgA1与人脐静脉内皮细胞结合量的研究[J]. 北京大学学报(医学版), 2005, 37(2): 139-142.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
[1] 田增民, 陈涛, Nanbert ZHONG, 李志超, 尹丰, 刘爽. 神经干细胞移植治疗遗传性小脑萎缩的临床研究(英文稿)[J]. 北京大学学报(医学版), 2009, 41(4): 456 -458 .
[2] 郭岩, 谢铮. 用一代人时间弥合差距——健康社会决定因素理论及其国际经验[J]. 北京大学学报(医学版), 2009, 41(2): 125 -128 .
[3] 成刚, 钱振华, 胡军. 艾滋病项目自愿咨询检测的技术效率分析[J]. 北京大学学报(医学版), 2009, 41(2): 135 -140 .
[4] 卢恬, 朱晓辉, 柳世庆, 郑杰, 邱晓彦. 白细胞介素2促进宫颈癌细胞系HeLaS3免疫球蛋白G的表达[J]. 北京大学学报(医学版), 2009, 41(2): 158 -161 .
[5] 袁惠燕, 张苑, 范田园. 离子交换型栓塞微球及其载平阳霉素的制备与性质研究[J]. 北京大学学报(医学版), 2009, 41(2): 217 -220 .
[6] 徐莉, 孟焕新, 张立, 陈智滨, 冯向辉, 释栋. 侵袭性牙周炎患者血清中抗牙龈卟啉单胞菌的IgG抗体水平的研究[J]. 北京大学学报(医学版), 2009, 41(1): 52 -55 .
[7] 祁琨, 邓芙蓉, 郭新彪. 纳米二氧化钛颗粒对人肺成纤维细胞缝隙连接通讯的影响[J]. 北京大学学报(医学版), 2009, 41(3): 297 -301 .
[8] Jian-wei GU, Emily YOUNG, Zhi-jun PAN, Kevan B. TUCKER, Megan SHPARAGO, Min HUANG, Amelia Purser BAILEY. SD大鼠长期高盐饮食可导致其高血压并改变肾细胞因子基因表达谱[J]. 北京大学学报(医学版), 2009, 41(5): 505 -515 .
[9] 李宏亮*, 安卫红*, 赵扬玉, 朱曦. 妊娠合并高脂血症性胰腺炎行血液净化治疗1例[J]. 北京大学学报(医学版), 2009, 41(5): 599 -601 .
[10] 李伟军, 邢晓芳, 曲立科, 孟麟, 寿成超. PRL-3基因C104S位点突变体和CAAX缺失体的构建及表达[J]. 北京大学学报(医学版), 2009, 41(5): 516 -520 .