Cell state transition analysis identifies interventions that improve control of Mycobacterium tuberculosis infection by susceptible macrophages

被引:2
|
作者
Yabaji, Shivraj M. [1 ]
Rukhlenko, Oleksii S. [2 ]
Chatterjee, Sujoy [1 ]
Bhattacharya, Bidisha [1 ]
Wood, Emily [2 ]
Kasaikina, Marina [1 ]
Kholodenko, Boris N. [2 ,3 ,4 ]
Gimelbrant, Alexander A. [5 ]
Kramnik, Igor [1 ,6 ,7 ]
机构
[1] Boston Univ, Natl Emerging Infect Dis Labs NEIDL, Boston, MA 02215 USA
[2] Univ Coll Dublin, Sch Med & Med Sci, Syst Biol Ireland, Belfield Dublin 4, Ireland
[3] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, Belfield Dublin 4, Ireland
[4] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06510 USA
[5] Altius Inst Biomed Sci, Seattle, WA USA
[6] Boston Univ, Sch Med, Dept Med, Pulm Ctr, Boston, MA 02118 USA
[7] Boston Univ, Sch Med, Dept Microbiol, Boston, MA 02118 USA
来源
SCIENCE ADVANCES | 2023年 / 9卷 / 39期
基金
美国国家卫生研究院;
关键词
PATHOGENESIS; RESISTANT;
D O I
10.1126/sciadv.adh4119
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding cell state transitions and purposefully controlling them to improve therapies is a longstanding challenge in biological research and medicine. Here, we identify a transcriptional signature that distinguishes activated macrophages from the tuberculosis (TB) susceptible and resistant mice. We then apply the cSTAR (cell state transition assessment and regulation) approach to data from screening-by-RNA sequencing to identify chemical perturbations that shift the transcriptional state of tumor necrosis factor (TNF)-activated TB-susceptible macrophages toward that of TB-resistant cells, i.e., prevents their aberrant activation without suppressing beneficial TNF responses. Last, we demonstrate that the compounds identified with this approach enhance the resistance of the TB-susceptible mouse macrophages to virulent Mycobacterium tuberculosis.
引用
收藏
页数:14
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