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Enhanced T-cell activation and chemokine-associated function in CD14-positive cells from venous sinus blood in sub-acute cerebral venous sinus thrombosis.

Authors :
Chang, Yu-Zhou
Song, Yu-Qi
Zhu, Hao-Yu
Zhang, Jia-Rui
Fu, Xi-Guang
Wang, Yi-Long
Dong, Ke-Hui
Jiang, Chu-Han
Mo, Da-Peng
Zhang, Yu-Peng
Source :
Frontiers in Cell & Developmental Biology; 2024, p1-11, 11p
Publication Year :
2024

Abstract

Background: Patients with sub-acute cerebral venous sinus thrombosis experience (SA.CVST) severe symptoms compared to two other venous sinus-related diseases, including chronic cerebral venous sinus thrombosis (C.CVST) and idiopathic intracranial hypertension (IIH). Objective: This study aimed to determine whether the different immune reactions in different venous sinuses are related. Methods: Stagnant blood in the cerebral venous sinuses was extracted by passing a microcatheter and CD14 -positive cells were sorted by magnetic beads and subjected to RNA-seq sequencing. Results: Compared to patients with IIH, 128 genes were significantly down-regulated and 373 genes were significantly up-regulated in the sub-acute CVST samples. The functions of these genes were mainly focused on "immune response", "T cell activation" and "plasma membrane". Gene Set Enrichment Analysis (GSEA) showed T cell survival and activation-related function significantly unregulated in sub-acute CVST. On the other hand, there were 366 genes down-regulated in chronic CVST and 75 genes up-regulated in chronic CVST. In functional annotation, these differently expressed genes were enriched in the "extracellular region", "chemokine-mediated signaling pathway" and "immune response". GSEA analysis confirmed that chemokine-related functions were all up-regulated in sub-acute CVST and monocyte-macrophage adhesion functions were also significantly up-regulated. Conclusion: This study suggested the CD14 -positive created an activated immune response in sub-acute CVST. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2296634X
Database :
Complementary Index
Journal :
Frontiers in Cell & Developmental Biology
Publication Type :
Academic Journal
Accession number :
181131505
Full Text :
https://doi.org/10.3389/fcell.2024.1488005