Proton-Activated Chloride Channel 1 (PACC1) is essential for innate host defense against bacterial sepsis

Bacterial sepsis remains a major global health burden. Here, we report an essential role for the recently discovered acid-sensitive chloride channel, PACC1 (PAC/ASOR/TMEM206), in protective host defense during bacterial infection and sepsis. PACC1 is highly expressed in human and mouse phagocytic myeloid cells, particularly macrophages, where it regulates phagocytic bacterial clearance and inflammatory responses. Using <i>de novo</i> generated mice, we show that global or myeloid cell-targeted deletion of PACC1 impairs development of phagolysosomal acidification, confers susceptibility to bacterial infection and excessive inflammation, and undermines host defense. These findings warrant further investigation of PACC1 in sepsis pathobiology.

Authors

Institutions

Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-02
DOI
https://doi.org/10.64898/2025.12.31.697179
Primary Topic
Ion Transport and Channel Regulation
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Proton-Activated Chloride Channel 1 (PACC1) is essential for innate host defense against bacterial sepsis

Seung Hoan Choi, Matthew M. Helmkamp, Marcel Strueve, Sarah Walachowski et al.
bioRxiv (Cold Spring Harbor Laboratory)
Ion Transport and Channel Regulation
article

Proton-Activated Chloride Channel 1 (PACC1) is essential for innate host defense against bacterial sepsis

Seung Hoan Choi, Matthew M. Helmkamp, Marcel Strueve, Sarah Walachowski, Lucien P. Garo, Kevin Brueck, Shuang Xu, Christoph Reinhardt, Archana Jayaraman, Markus Bosmann, Hulbert Yang
article en

Abstract

Bacterial sepsis remains a major global health burden. Here, we report an essential role for the recently discovered acid-sensitive chloride channel, PACC1 (PAC/ASOR/TMEM206), in protective host defense during bacterial infection and sepsis. PACC1 is highly expressed in human and mouse phagocytic myeloid cells, particularly macrophages, where it regulates phagocytic bacterial clearance and inflammatory responses. Using <i>de novo</i> generated mice, we show that global or myeloid cell-targeted deletion of PACC1 impairs development of phagolysosomal acidification, confers susceptibility to bacterial infection and excessive inflammation, and undermines host defense. These findings warrant further investigation of PACC1 in sepsis pathobiology.

bioRxiv (Cold Spring Harbor Laboratory)
Boston University (US), Johannes Gutenberg University Mainz (DE), University Medical Center of the Johannes Gutenberg University Mainz (DE), German Centre for Cardiovascular Research (DE)
Openalex Percentile: Top 99%
Ion Transport and Channel Regulation
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Proton-Activated Chloride Channel 1 (PACC1) is essential for innate host defense against bacterial sepsis — Seung Hoan Choi, Matthew M. Helmkamp, et al. · bioRxiv (Cold Spring Harbor Laboratory) (2026) | TGRS Research Map | TGRS