Single‐cell atlas of peripheral blood by CyTOF revealed peripheral blood immune cells metabolic alterations and neutrophil changes in intracranial aneurysm rupture

Author:

Ya Xiaolong12,Liu Chenglong12,Ma Long12,Ge Peicong12,Xu Xiaoxue3,Zheng Zhiyao14,Mou Siqi5,Wang Rong12,Zhang Qian12,Ye Xun12,Zhang Dong16,Zhang Yan12,Wang Wenjing7,Li Hao12,Zhao Jizong12

Affiliation:

1. Department of Neurosurgery, Beijing Tiantan Hospital Capital Medical University Beijing China

2. China National Clinical Research Center for Neurological Diseases Beijing China

3. Department of Core Facility Center Capital Medical University Beijing China

4. Department of Neurosurgery, Peking Union Medical College Hospital Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China

5. Medical School University of Chinese Academy of Sciences Beijing China

6. Department of Neurosurgery Beijing Hospital Beijing China

7. Beijing Institute of Hepatology, Beijing YouAn Hospital Capital Medical University Beijing China

Abstract

AbstractPrevious studies have found that the peripheral immune environment is closely related to the occurrence and development of intracranial aneurysms. However, it remains unclear how the metabolism of peripheral blood mononuclear cells (PBMCs) and the composition of polymorphonuclear leukocytes (PMNs) changes in the process of intracranial aneurysm rupture. This study utilized cytometry by time of flight technology to conduct single‐cell profiling analysis of PBMCs and PMNs from 72 patients with IAs. By comparing the expression differences of key metabolic enzymes in PBMCs between patients with ruptured intracranial aneurysms (RIAs) and unruptured intracranial aneurysms, we found that most PBMCs subsets from RIA group showed upregulation of rate‐limiting enzymes related to the glycolytic pathway. By comparing the composition of PMNs, it was found that the proinflammatory CD101+HLA DR+ subsets were increased in the RIA group, accompanied by a decrease in the anti‐inflammatory polymorphonuclear myeloid‐derived suppressor cells. In conclusion, this study showed the changes in the peripheral immune profile of RIAs, which is helpful for our understanding of the mechanisms underlying peripheral changes and provides a direction for future related research.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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