生物技术进展 ›› 2024, Vol. 14 ›› Issue (4): 649-656.DOI: 10.19586/j.2095-2341.2024.0032

• 研究论文 • 上一篇    

新型冠状病毒奥密克戎感染下血小板转录组与蛋白质组的对比分析

马叶子1,2(), 夏美娟1,2, 刘翠翠1,2, 王洪涛1,2, 周家喜1,2()   

  1. 1.中国医学科学院血液病医院(中国医学科学院血液学研究所)北京协和医学院,血液与健康全国重点实验室,国家血液系统疾病临床医学研究中心,细胞生态海河实验室,天津 300020
    2.天津医学健康研究院,天津 301600
  • 收稿日期:2024-02-27 接受日期:2024-04-22 出版日期:2024-07-25 发布日期:2024-08-07
  • 通讯作者: 周家喜
  • 作者简介:马叶子E-mail: mayezi@ihcams.ac.cn
  • 基金资助:
    中国医学科学院医学与健康科技创新工程项目(2021-I2M-1-073);天津市科技计划青年项目(22JCQNJC01270)

Comparative Analysis of Platelet Transcriptome and Proteome Changes in SARS-CoV2 Omicron Infection

Yezi MA1,2(), Meijuan XIA1,2, Cuicui LIU1,2, Hongtao WANG1,2, Jiaxi ZHOU1,2()   

  1. 1.State Key Laboratory of Experimental Hematology,National Clinical Research Center for Blood Diseases,Haihe Laboratory of Cell Ecosystem,Institute of Hematology & Blood Diseases Hospital,Chinese Academy of Medical Sciences & Peking Union Medical College,Tianjin 300020,China
    2.Tianjin Institutes of Health Science,Tianjin 301600,China
  • Received:2024-02-27 Accepted:2024-04-22 Online:2024-07-25 Published:2024-08-07
  • Contact: Jiaxi ZHOU

摘要:

血小板是维持机体稳态和应对疾病感染等的关键血液成分,其无核特征以及转录本和蛋白质来源的多样性导致血小板的转录组和蛋白组相关性普遍偏低。前期研究已解析了血小板蛋白质组在新型冠状病毒(severe acute respiratory syndrome coronavirus 2,SARS-CoV2)奥密克戎感染不同阶段的动态表达模式,但对其具体来源未作深入分析。为了解血小板对奥密克戎感染的应答机制,对血小板蛋白组与转录本进行了对比分析,以探究不同蛋白分子的来源。结果发现,血小板转录组变化相较于蛋白组更为剧烈,且二者的变化存在差异。感染后血小板转录组与蛋白组共同上调的基因/蛋白主要富集了固有免疫、抗病毒免疫反应等特征,提示相关蛋白可能来自血小板内RNA翻译。血小板蛋白组单独上调的蛋白特征包括急性炎症反应、吞噬识别作用等,提示该部分蛋白可能由血浆直接摄入或与其他细胞互作所得。此外,血小板转录组也单独上调RNA代谢过程、RNA剪接的调控等相关基因。研究结果为探究奥密克戎感染条件下血小板RNA和蛋白质的来源多样性提供了重要的数据支撑。

关键词: 奥密克戎, 血小板, 转录组, 蛋白组

Abstract:

As an important blood component, platelets play a key role in the maintenance of homeostasis and the stress of diseases infection. The absence of nuclei and the diversity of transcripts and protein sources lead to a generally low transcriptomic and proteomic correlation of platelets. Previous research have analyzed the dynamic expression patterns of platelet proteome at different stages of severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) Omicron infection, but the specific sources have not been thoroughly analyzed. In order to further understand the mechanism of platelet response in Omicron infection, we compared the platelet proteome with the transcript to explore the sources of different protein molecules. The results showed that the changes of platelet transcriptome were more drastic than those of proteome, and the changes of the two were different. The genes/proteins co-upregulated by platelet transcriptome and proteome after infection mainly enriched innate immunity and antiviral immune response, suggesting that related proteins may be derived from RNA translation in platelets. The upregulation features of platelet proteome included acute inflammatory response and phagocytosis recognition, suggesting that this part of the protein may be obtained by direct plasma intake or interaction with other cells. In addition, platelet transcriptome also independently up-regulated RNA metabolism and RNA splicing regulation and other related genes. This study provides important data support for exploring the diversity of platelet RNA and protein sources under Omicron infection.

Key words: Omicron, platelets, transcriptome, proteome

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