General Information of HIF (ID: HIFC0019)
HIF Name
M1 macrophages
HIF Synonym(s)
M1 macrophage, M1 macrophages
HIF Classification
Macrophages (Mac)
Description M1 macrophages are responsible for phagocytosis and regulation of the pro-inflammatory response through antigen presentation as well as chemokine and cytokine production [1]
Microbe Species (MIC) Regulated by This HIF
         Aggregatibacter actinomycetemcomitans (gamma-proteobacteria) MIC00051
             Description Aggregatibacter actinomycetemcomitans induced predominantly pro-inflammatory (M1 macrophages-like phenotypes) responses. [2]
         Bacteroides fragilis (CFB bacteria) MIC00158
             Description Bacteroides fragilis was significantly decreased with methotrexate treatment(P < 0.01) and tended to decrease proportionately with increasing M1 macrophages density. [3]
         Bifidobacterium pseudolongum (actinobacteria) MIC00220
             Description Cell free extract from Bifidobacterium pseudolongum had effects at mitigating M1-differentiation of macrophages. [4]
         Candida albicans (budding yeasts) MIC00317
             Description The Candida albicans may kill or inactivate to inhibit the M1 macrophages formation and block macrophage antimicrobial activity. [2]
         Desulfovibrio vulgaris (delta-proteobacteria) MIC00502
             Description The ratio of M1/M2 colonic macrophage was greatly increased by the Desulfovibrio vulgaris. [5]
         Fusobacterium nucleatum (fusobacteria) MIC00617
             Description Fusobacteria nucleatum AI-2 enhanced M1 polarization of macrophages, possibly through TNFSF9/TRAF1/p-AKT/IL-1signaling. [6]
         Parabacteroides distasonis (CFB bacteria) MIC00949
             Description Consistent with an overall anti-inflammatory status, the abundance of Parabacteroides increased when decreases in M1 macrophages.. [7]
         Porphyromonas gingivalis (CFB bacteria) MIC01000
             Description Porphyromonas gingivalis induced predominantly pro-inflammatory (M1 macrophages-like phenotypes) responses. [2]
References
1 Macrophage and nerve interaction in endometriosis.J Neuroinflammation. 2017 Mar 14;14(1):53. doi: 10.1186/s12974-017-0828-3.
2 Oral Microbiota and Immune System Crosstalk: A Translational Research.Biology (Basel). 2020 Jun 16;9(6):131. doi: 10.3390/biology9060131.
3 Induction and Amelioration of Methotrexate-Induced Gastrointestinal Toxicity are Related to Immune Response and Gut Microbiota.EBioMedicine. 2018 Jul;33:122-133. doi: 10.1016/j.ebiom.2018.06.029. Epub 2018 Jul 2.
4 The Pancreatic Cancer Microbiome Promotes Oncogenesis by Induction of Innate and Adaptive Immune Suppression.Cancer Discov. 2018 Apr;8(4):403-416. doi: 10.1158/2159-8290.CD-17-1134. Epub 2018 Mar 22.
5 Glabridin Prevents Doxorubicin-Induced Cardiotoxicity Through Gut Microbiota Modulation and Colonic Macrophage Polarization in Mice.Front Pharmacol. 2019 Feb 15;10:107. doi: 10.3389/fphar.2019.00107. eCollection 2019.
6 Autoinducer-2 of Fusobacterium nucleatum promotes macrophage M1 polarization via TNFSF9/IL-1 signaling.Int Immunopharmacol. 2019 Sep;74:105724. doi: 10.1016/j.intimp.2019.105724. Epub 2019 Jul 1.
7 Chronic oral exposure to glycated whey proteins increases survival of aged male NOD mice with autoimmune prostatitis by regulating the gut microbiome and anti-inflammatory responses. Food Funct. 2020 Jan 29;11(1):153-162. doi: 10.1039/c9fo01740b.

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