Evidence map›Paper›PMID 33368247›Full record

ArticleJournal of cellular physiology2021

PLD1 and PLD2 differentially regulate the balance of macrophage polarization in inflammation and tissue injury.

Won Chan Hwang, Seol Hwa Seo, Minju Kang, Rae Hee Kang, Gilbert Di Paolo, Kang-Yell Choi, Do Sik Min

Open access · hybridAbstract read
In one paragraph

Article in Journal of cellular physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  4. Longitudinal associations between PMFrontiers in cellular and infection microbiology · 2026
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  5. Novel compound heterozygous variants in theFrontiers in cardiovascular medicine · 2026
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  6. Review
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  10. PLD2 deletion ameliorates sepsis-induced cardiomyopathy by suppressing cardiomyocyte pyroptosis via the NLRP3/caspase 1/GSDMD pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
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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

7 authors at 2 institutions in 2 countries.

Won Chan HwangCollege of Pharmacy, Yonsei University, Incheon, Republic of Korea.
Seol Hwa SeoDepartment of Biotechnology, Yonsei University, Seoul, Republic of Korea.
Minju KangCollege of Pharmacy, Yonsei University, Incheon, Republic of Korea.
Rae Hee KangCollege of Pharmacy, Yonsei University, Incheon, Republic of Korea.
Gilbert Di PaoloDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York City, New York, USA.
Kang-Yell ChoiDepartment of Biotechnology, Yonsei University, Seoul, Republic of Korea.
Do Sik MinCollege of Pharmacy, Yonsei University, Incheon, Republic of Korea.ORCID 0000-0002-8570-5098
Yonsei University · KRColumbia University Irving Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phospholipase D (PLD) isoforms PLD1 and PLD2 serve as the primary nodes where diverse signaling pathways converge. However, their isoform-specific functions remain unclear. We showed that PLD1 and PLD2 selectively couple to toll-like receptor 4 (TLR4) and interleukin 4 receptor (IL-4R) and differentially regulate macrophage polarization of M1 and M2 via the LPS-MyD88 axis and the IL-4-JAK3 signaling, respectively. Lipopolysaccharide (LPS) enhanced TLR4 or MyD88 interaction with PLD1; IL-4 induced IL-4R or JAK3 association with PLD2, indicating isozyme-specific signaling events. PLD1 and PLD2 are indispensable for M1 polarization and M2 polarization, respectively. Genetic and pharmacological targeting of PLD1 conferred protection against LPS-induced sepsis, cardiotoxin-induced muscle injury, and skin injury by promoting the shift toward M2; PLD2 ablation intensified disease severity by promoting the shift toward M1. Enhanced Foxp3

Indexed as

AnimalsCell PolarityInflammationJanus Kinase 3LipopolysaccharidesMacrophagesMiceMice, Inbred C57BLMice, KnockoutMusclesMyeloid Differentiation Factor 88Phospholipase DReceptors, Interleukin-4SepsisT-Lymphocytes, RegulatoryToll-Like Receptor 4Jak3 protein, mouseJanus Kinase 3LipopolysaccharidesMyd88 protein, mouseMyeloid Differentiation Factor 88Phospholipase Dphospholipase D1phospholipase D2Receptors, Interleukin-4Tlr4 protein, mouseToll-Like Receptor 4IL-4Rinflammationmacrophage polarizationphospholipase Dtissue homeostasisTLR-4

Identifiers

PMID33368247
PMCPMC8048932
OpenAlexW3117686882

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.