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Region-Specific CD16 + Neutrophils Promote Colorectal Cancer Progression by Inhibiting Natural Killer Cells.

Authors :
Zhang Y
Wang Z
Lu Y
Sanchez DJ
Li J
Wang L
Meng X
Chen J
Kien TT
Zhong M
Gao WQ
Ding X
Source :
Advanced science (Weinheim, Baden-Wurttemberg, Germany) [Adv Sci (Weinh)] 2024 Aug; Vol. 11 (29), pp. e2403414. Date of Electronic Publication: 2024 May 24.
Publication Year :
2024

Abstract

The colon is the largest compartment of the immune system, with innate immune cells exposed to antigens in the environment. However, the mechanisms by which the innate immune system is instigated are poorly defined in colorectal cancer (CRC). Here, a population of CD16 <superscript>+</superscript> neutrophils that specifically accumulate in CRC tumor tissues by imaging mass cytometry (IMC), immune fluorescence, and flow cytometry, which demonstrated pro-tumor activity by disturbing natural killer (NK) cells are identified. It is found that these CD16 <superscript>+</superscript> neutrophils possess abnormal cholesterol accumulation due to activation of the CD16/TAK1/NF-κB axis, which upregulates scavenger receptors for cholesterol intake including CD36 and LRP1. Consequently, these region-specific CD16 <superscript>+</superscript> neutrophils not only competitively inhibit cholesterol intake of NK cells, which interrupts NK lipid raft formation and blocks their antitumor signaling but also release neutrophil extracellular traps (NETs) to induce the death of NK cells. Furthermore, CD16-knockout reverses the pro-tumor activity of neutrophils and restored NK cell cytotoxicity. Collectively, the findings suggest that CRC region-specific CD16 <superscript>+</superscript> neutrophils can be a diagnostic marker and potential therapeutic target for CRC.<br /> (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)

Details

Language :
English
ISSN :
2198-3844
Volume :
11
Issue :
29
Database :
MEDLINE
Journal :
Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Publication Type :
Academic Journal
Accession number :
38790136
Full Text :
https://doi.org/10.1002/advs.202403414