Evidence map›Paper›PMID 40558486›Full record

ArticleCells2025

B10 Promotes Polarization and Pro-Resolving Functions of Bone Marrow Derived Macrophages (BMDM) Through PD-1 Activation.

Takumi Memida, Guoqin Cao, Elaheh Dalir Abdolahinia, Sunniva Ruiz, Shengyuan Huang, Sahar Hassantash, Satoru Shindo, Motoki Okamoto, Shohei Yamashita, Shin Nakamura and 3 more

Abstract read
In one paragraph

Article in Cells, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Takumi MemidaDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.ORCID 0009-0004-9524-9462
Guoqin CaoDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.
Elaheh Dalir AbdolahiniaDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.
Sunniva RuizDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.
Shengyuan HuangDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.
Sahar HassantashDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.ORCID 0000-0003-4094-4121
Satoru ShindoDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.
Motoki OkamotoDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.ORCID 0000-0002-3759-5031
Shohei YamashitaDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.ORCID 0009-0009-4360-2830
Shin NakamuraDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.
Maiko SuzukiDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.ORCID 0000-0002-1732-0663
Toshihisa KawaiDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.
Xiaozhe HanDepartment of Oral Science and Translational Research, College of Dental Medicine, Nova Southeastern University, 3301 South University Drive, Fort Lauderdale, FL 33314, USA.ORCID 0000-0001-8357-1471

Funding

Regulatory B Cells in the Amelioration of Immune-Mediated Periodontal DiseaseR01DE025255 · NIDCR · NOVA SOUTHEASTERN UNIVERSITY · PI HAN, XIAOZHE · 2015 to 2025
$5.8M
Role of OC-STAMP expressed on human osteoclasts in periodontitisR01DE029709 · NIDCR · NOVA SOUTHEASTERN UNIVERSITY · PI KAWAI, TOSHIHISA · 2020 to 2025
$2.8M
Epigenetic and Non-epigenetic Role of SIRT1 in Fluoride-induced Cell Stress Administrative Supplement.R01DE027648 · NIDCR · OHIO STATE UNIVERSITY · PI SUZUKI, MAIKO · 2018 to 2024
$2.2M
Linear Ion Trap - Quadrupole LC-MS SystemS10OD032292 · OD · WAYNE STATE UNIVERSITY · PI MADDIPATI, KRISHNARAO · 2022 to 2022
$592k
Health Effects of the Fluorinated Pollutants; PFAS on Enamel DevelopmentK02DE029531 · NIDCR · NOVA SOUTHEASTERN UNIVERSITY · PI SUZUKI, MAIKO · 2022 to 2024
$428k
NIDCR NIH HHS DE025255NIDCR NIH HHS DE027648NIDCR NIH HHS DE029709NIDCR NIH HHS K02 DE029531NIDCR NIH HHS R01 DE025255NIDCR NIH HHS R01 DE027648NIDCR NIH HHS R01 DE029709NIH HHS S10 OD032292
6 · The paper itself

Abstract

Regulatory B cells (B regs) are immune cells that help suppress excessive inflammatory responses by interacting with other immune components. Among them, B-10 cells are known for their strong immunoregulatory function. This study focused on how B-10 cells influence macrophage phenotype and function through the PD-1 signaling pathway. To investigate this, B-10 cells derived from mouse spleens were co-cultured with bone marrow-derived macrophages (BMDMs) from either wild-type (WT) or PD-1 knockout (PD-1 KO) mice, using both direct contact and Transwell setups. The findings indicated that direct co-culture with B-10 cells significantly promoted the polarization of macrophages towards the anti-inflammatory M2 type, characterized by increased expression of surface markers (F4/80

Indexed as

Cell PolarityMacrophagesProgrammed Cell Death 1 ReceptorAnimalsCoculture TechniquesMacrophage ActivationMiceMice, Inbred C57BLMice, KnockoutPhagocytosisSignal TransductionPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorB10 cellsmacrophagePD-1regulatory B cellSPMs

Identifiers

PMID40558486
PMCPMC12191351

What OpenQuestion holds

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Registered trials

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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.