上海交通大学学报(医学版) ›› 2021, Vol. 41 ›› Issue (4): 413-420.doi: 10.3969/j.issn.1674-8115.2021.04.001

• 论著·基础研究 • 上一篇    下一篇

酶消化细胞团块法对人胚胎干细胞中OCT4与SOX2蛋白水平的影响

孙潇智(), 李爽, 金颖(), 廖兵()   

  1. 上海交通大学基础医学院组织胚胎与遗传发育学系,上海 200025
  • 收稿日期:2020-05-14 出版日期:2021-04-28 发布日期:2021-05-14
  • 通讯作者: 金颖,廖兵 E-mail:zdsxz@126.com;yjin@sibs.ac.cn;liaobing@shsmu.edu.cn
  • 作者简介:孙潇智(1994—),男,硕士生;电子信箱:zdsxz@126.com
  • 基金资助:
    国家重点研发计划(2016YFA0100101);上海交通大学医学院高水平地方高校创新团队(SSMU-ZLCX20180401)

Effect of enzyme digestion into cell clumps on protein levels of OCT4 and SOX2 in human embryonic stem cells

Xiao-zhi SUN(), Shuang LI, Ying JIN(), Bing LIAO()   

  1. Department of Histoembryology, Genetics & Development, Shanghai Jiao Tong University College of Basic Medical Sciences, Shanghai 200025, China
  • Received:2020-05-14 Online:2021-04-28 Published:2021-05-14
  • Contact: Ying JIN,Bing LIAO E-mail:zdsxz@126.com;yjin@sibs.ac.cn;liaobing@shsmu.edu.cn
  • Supported by:
    National Key R & D Plan(2016YFA0100101);Innovative Research Team of High-Level Local Universities in Shanghai(SSMU-ZLCX20180401)

摘要:

目的·探究酶消化细胞团块法对人胚胎干细胞(human embryonic stem cell,hESC)的八聚体结合转录因子4(octamer-binding protein 4,OCT4)和性别决定区Y框蛋白2(sex determining region Y-box 2,SOX2)蛋白水平的影响及可能的作用机制。方法·①利用Western blotting分析检测酶消化细胞团块法[分散酶Dispase或胶原酶Ⅳ(collagenase type Ⅳ,COL4)]、酶消化单细胞法(细胞分离溶液Accutase或胰酶)和机械刮取法对hESC中OCT4和SOX2蛋白水平的影响。②使用金属离子螯合剂乙二醇双(2-氨基乙醚)四乙酸(EGTA)破坏hESC-hESC细胞间连接,然后利用Western blotting检测EGTA单独处理或联合COL4处理对hESC中OCT4与SOX2的蛋白水平的影响。③通过基于质谱的定量蛋白质组学技术,检测COL4单独处理或与EGTA联合处理hESC细胞样本中差异表达的磷酸化蛋白和总蛋白,并进行功能富集分析。④利用Western blotting和免疫荧光染色检测蛋白酶体抑制剂bortezomib或溶酶体抑制剂氯喹预处理对COL4引起的hESC中OCT4与SOX2蛋白水平下调的影响。⑤利用Western blotting检测COL4对丝切蛋白(cofilin)的影响,以及Rac1小分子抑制剂EHT1864和EHop-016对SOX2蛋白表达水平的影响。结果·①COL4和Dispase引起OCT4和SOX2的蛋白水平下降;Accutase、胰酶和机械刮取法未观察到此作用。②EGTA处理能够抑制COL4消化hESC引起的OCT4和SOX2蛋白水平下降。③蛋白质谱和功能富集分析发现,COL4消化hESC引起的OCT4和SOX2蛋白水平下降可能与肌动蛋白微丝(actin filament,F-actin)、微管和溶酶体相关蛋白的变化有关。④氯喹能够抑制COL4消化hESC引起的OCT4和SOX2蛋白水平下降,bortezomib则不能。⑤COL4处理或Rac1抑制剂均能下调cofilin和SOX2的蛋白水平。结论·当使用酶消化细胞团块法处理hESC时,OCT4和SOX2蛋白水平下降,Rac1/cofilin/F-actin信号通路和溶酶体可能参与其中。

关键词: 人胚胎干细胞, 细胞外基质, 八聚体结合转录因子4, 性别决定区Y框蛋白2, 溶酶体, 丝切蛋白

Abstract:

Objective· To reveal the effect of enzyme digestion into cell clumps on protein levels of octamer-binding protein 4 (OCT4) and sex determining region Y-box 2 (SOX2) in the human embryonic stem cells (hESCs) and its possible molecular mechanism.

Methods· ① Western blotting was conducted to detect the protein levels of OCT4 and SOX2 in the hESCs treated by enzyme digestion into cell clumps [Dispase or collagenase type Ⅳ (COL4)], enzyme digestion into single cells (Accutase or trypsin), or mechanical scraping dissociation. ② Ethylene glycol tetraacetic acid (EGTA) was used to destruct hESC-hESC interaction, and protein levels of OCT4 and SOX2 in the hESCs treated with EGTA alone or combined with COL4 were detected by Western blotting. ③ Quantitative proteomics analysis based on mass spectrometry was carried out to identify differentially expressed total proteins and phosphorylated proteins in the hESCs treated with COL4 alone or in combination with EGTA. ④ hESCs were pre-treated with proteasome inhibitor (bortezomib) and lysosome inhibitor (chloroquine), respectively, followed by Western blotting and immunofluorescence staining to measure their effects on COL4-induced down regulation of OCT4 and SOX2. ⑤ Western blotting analysis was conducted to test the effect of COL4 treatment on cofilin as well as Rac1 inhibitors (EHT1864 and EHop-016) treatment on the protein level of SOX2 in the hESCs.

Results· ① COL4 or Dispase treatment led to protein levels decrease of OCT4 and SOX2, while Accutase, trypsin and mechanical dissociation did not elicit such effect. ② EGTA rescued OCT4 and SOX2 protein levels decrease indcued by COL4 treatment. ③Quantitative mass spectrometry and functional enrichment analysis suggested that microtubule, actin filament (F-actin) and lysosome-associated proteins might be related to OCT4 and SOX2 protein levels decline in the suspended clumps of hESCs upon COL4 treatment. ④Chloroquine, instead of bortezomib, could block COL4-induced protein levels decrease of OCT4 and SOX2. ⑤The treatment of COL4 or Rac1 inhibitors could downregulate protein levels of cofilin and SOX2.

Conclusion· Upon hESC detachment in cell clumps induced by enzyme treatment, the protein levels of SOX2 and OCT4 decline, which may be related to Rac1/cofilin/F-actin signaling pathway and lysosome.

Key words: human embryonic stem cell (hESC), extracellular matrix (ECM), octamer-binding protein 4 (OCT4), sex determining region Y-box 2 (SOX2), lysosome, cofilin

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