脂多糖
转录组
生物
败血症
炎症
先天免疫系统
基因
自噬
狒狒
蛋白质组
细胞凋亡
细胞生物学
免疫学
基因表达
微生物学
遗传学
生态学
免疫系统
作者
David J. Gregory,Feifei Han,Peng Li,Marina Gritsenko,Jennifer Kyle,Frank E. Riley,Deborah Chavez,Vania Yotova,Renata Sindeaux,Mohamed B. F. Hawash,Fengyun Xu,Li-Yuan Hung,Ivor S. Douglas,Ron G. Tompkins,Robert E. Lanford,Lester Kobzik,Judith Hellman,Jonathan M. Jacobs,Luis B. Barreiro,Wenzhong Xiao
出处
期刊:Cold Spring Harbor Laboratory - medRxiv
日期:2023-11-30
被引量:1
标识
DOI:10.1101/2023.11.30.23299243
摘要
Vertebrates differ greatly in responses to pro-inflammatory agonists such as bacterial lipopolysaccharide (LPS), complicating use of animal models to study human sepsis or inflammatory disorders. We compared transcriptomes of resting and LPS-exposed blood from six LPS-sensitive species (rabbit, pig, sheep, cow, chimpanzee, human) and four LPS-resilient species (mice, rats, baboon, rhesus), as well as plasma proteomes and lipidomes. Unexpectedly, at baseline, sensitive species already had enhanced expression of LPS-responsive genes relative to resilient species. After LPS stimulation, maximally different genes in resilient species included genes that detoxify LPS, diminish bacterial growth, discriminate sepsis from SIRS, and play roles in autophagy and apoptosis. The findings reveal the molecular landscape of species differences in inflammation, and may inform better selection of species for pre-clinical models.
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