Early Atf4 activity drives airway club and goblet cell differentiation

被引:2
|
作者
Barrera-Lopez, Juan F. [1 ]
Cumplido-Laso, Guadalupe [1 ]
Olivera-Gomez, Marcos [1 ]
Garrido-Jimenez, Sergio [1 ]
Diaz-Chamorro, Selene [1 ]
Mateos-Quiros, Clara M. [1 ]
Benitez, Dixan A. [1 ]
Centeno, Francisco [1 ]
Mulero-Navarro, Sonia [1 ]
Roman, Angel C. [1 ]
Carvajal-Gonzalez, Jose M. [1 ]
机构
[1] Univ Extremadura, Fac Formac Profesorade, Dept Bioquim Biol Mol & Genet, Badajoz, Spain
关键词
STEM-CELLS; TRANSCRIPTION FACTORS; GENE-EXPRESSION; DIOXIN RECEPTOR; LUNG; FOXJ1; DEDIFFERENTIATION; CILIOGENESIS; INHIBITION; FACTOR-4;
D O I
10.26508/lsa.202302284
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Activating transcription factor 4 (Atf4), which is modulated by the protein kinase RNA-like ER kinase (PERK), is a stress-induced transcription factor responsible for controlling the expression of a wide range of adaptive genes, enabling cells to withstand stressful conditions. However, the impact of the Atf4 signaling pathway on airway regeneration remains poorly understood. In this study, we used mouse airway epithelial cell culture models to investigate the role of PERK/Atf4 in respiratory tract differentiation. Through pharmacological inhibition and silencing of ATF4, we uncovered the crucial involvement of PERK/Atf4 in the differentiation of basal stem cells, leading to a reduction in the number of secretory cells. ChIP-seq analysis revealed direct binding of ATF4 to regulatory elements of genes associated with osteoblast differentiation and secretory cell function. Our findings provide valuable insights into the role of ATF4 in airway epithelial differentiation and its potential involvement in innate immune responses and cellular adaptation to stress.
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页数:14
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