Upexpression of BHLHE40 in gastric epithelial cells increases CXCL12 production through interaction with p-STAT3 in Helicobacter pylori-associated gastritis
posted on 2025-11-27, 00:50authored byYong-Sheng Teng, YL Zhao, MS Li, YG Liu, P Cheng, YP Lv, FY Mao, Weisan ChenWeisan Chen, SM Yang, CJ Hao, LS Peng, JY Zhang, WJ Zhang, QM Zou, Y Zhuang
<p dir="ltr">BHLHE40, a member of the basic helix-loop-helix transcription factor family, has been reported to play an important role in inflammatory diseases. However, the regulation and function of BHLHE40 in Helicobacter pylori (H pylori)-associated gastritis is unknown. </p><p dir="ltr">We observed that gastric BHLHE40 was significantly elevated in patients and mice with H pylori infection. Then, we demonstrate that H pylori-infected GECs express BHLHE40 via cagA-ERK pathway. BHLHE40 translocates to cell nucleus, and then binds to cagA protein-activated p-STAT3 (Tyr705). </p><p dir="ltr">The complex increases chemotactic factor CXCL12 expression (production). Release of CXCL12 from GECs fosters CD4<sup>+</sup>T cell infiltration in the gastric mucosa. </p><p dir="ltr">Our results identify the cagA-BHLHE40-CXCL12 axis that contributes to inflammatory response in gastric mucosa during H pylori infection.</p>
Funding
National Key Research and Development Program of China (grant number: 2016YFC1302200)
National Natural Science Foundation of China (grant number: 81870394 and 81372560)
History
Publication Date
2020-01-01
Journal
FASEB journal: Federation of American Societies for Experimental Biology