Evidence map›Paper›PMID 40999918›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Calhm6 Governs Macrophage Polarization Through Chp1-Camk4-Creb1 Axis and Ectosomal Delivery in Inflammatory Responses.

Yanlong Xin, Xiaofan Xiong, Yan Zhang, Siyu Zhang, Shuting Zhang, Yu Yang, Yingxue Liang, Lulu Zang, Xi Chen, Wenjuan Li and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Yanlong XinDepartment of General Surgery, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Xiaofan XiongDepartment of General Surgery, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Yan ZhangNational-Local Joint Engineering Research Center of Biodiagnosis & Biotherapy, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Siyu ZhangNational-Local Joint Engineering Research Center of Biodiagnosis & Biotherapy, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Shuting ZhangNational-Local Joint Engineering Research Center of Biodiagnosis & Biotherapy, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Yu YangNational-Local Joint Engineering Research Center of Biodiagnosis & Biotherapy, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Yingxue LiangInternational Joint Research Center on Cell Stress and Disease Diagnosis and Therapy, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Lulu ZangInternational Joint Research Center on Cell Stress and Disease Diagnosis and Therapy, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Xi ChenInternational Joint Research Center on Cell Stress and Disease Diagnosis and Therapy, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Wenjuan LiInternational Joint Research Center on Cell Stress and Disease Diagnosis and Therapy, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Issam HalalmehInternational Joint Research Center on Cell Stress and Disease Diagnosis and Therapy, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Rui ZhouDepartment of General Surgery, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Zongfang LiDepartment of General Surgery, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.
Haowen LiuSchool of Life Sciences and Technology, Xi'an Jiaotong University, Xi'an, 710049, China.
Jing GengDepartment of General Surgery, the Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710004, China.ORCID https://orcid.org/0000-0002-0568-7345

Funding

Basic Research Plan of Shaanxi Institute of Basic Science (Chemistry, Biology) 23JHQ060National Key Research and Development Program of China 2021YFA1100702National Natural Science Foundation of China 32070891National Natural Science Foundation of China 32370922National Natural Science Foundation of China 82201342National Natural Science Foundation of China 82201742National Natural Science Foundation of China 91842307Natural Science Basic Research Program of Shaanxi 2024JC-TBZC-23Scientific Research and Sharing Platform Construction Project of Shaanxi Province 2020JQ-556 (YX)Scientific Research and Sharing Platform Construction Project of Shaanxi Province 2022JQ-799 (XX)The Thousand Talents Plan of Shaanxi Province YJ0866The Young Talent Support Plan″ of Xi'an Jiaotong University (JG)Xi'an Project Medical Research General Project 24YXYJ0173 (JG)
6 · The paper itself

Abstract

Macrophage plasticity, critical for immune response, is often dysregulated in various infectious and inflammatory diseases. While ion channels have been implicated in immune cell modulation, how they influence macrophage polarization remains poorly understood. Here, it is demonstrated that ectosomes carrying the ion channel Calhm6 effectively suppress severe inflammation triggered by LPS. These Calhm6-bearing ectosomes, secreted by macrophages, facilitate M2-like polarization, elicit an anti-inflammatory response, and foster immune tolerance. Conversely, Calhm6 deficiency leads to suppressed Creb1 activity, which in turn augments M1-like macrophage polarization, enhancing bactericidal activity and the secretion of pro-inflammatory cytokines. Mechanistically, Chp1 serves as a scaffold protein and undergoes phosphorylation by CaMK4. This phosphorylation enhances the localization of the Calhm6-Chp1-CaMK4 complex to the cell membrane, promoting Creb1 activation and M2-like macrophage polarization calcium-dependently. Moreover, the M1-like polarization inducers LPS and IFNγ enhance the binding of Irf1 to the Calhm6 promoter, upregulating its expression and stimulating ectosome formation. Conversely, Stat6, activated by IL-4, competes with Irf1 for binding to the Calhm6 promoter, thereby suppressing its expression. In summary, our findings unravel the intricate interplay between ion channels, ectosomes, and macrophage polarization, revealing that ectosomal-Calhm6 can serve as a novel therapeutic agent to modulate inflammatory responses and facilitate tissue repair.

Indexed as

Calcium-Calmodulin-Dependent Protein Kinase Type 4Calcium ChannelsCyclic AMP Response Element-Binding ProteinInflammationMacrophagesAnimalsCell PolarityLipopolysaccharidesMacrophage ActivationMiceMice, Inbred C57BLCalcium-Calmodulin-Dependent Protein Kinase Type 4Calcium ChannelsCamk4 protein, mouseCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinLipopolysaccharidesCalhm6ectosomesinflammatory responseion channelmacrophage polarization

Identifiers

PMID40999918
PMCPMC12766987

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.