Details of Host Immune Factor (HIF) Regulating Microbe Species (MIC)
General Information of HIF (ID: HIFC0019) | |||||
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HIF Name |
M1 macrophages
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HIF Synonym(s) |
M1 macrophage, M1 macrophages
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HIF Classification |
Macrophages (Mac)
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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 | |||||
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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] | |||
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