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2023/02/23阅读:40主题:姹紫
文献阅读003:单细胞肿瘤浸润性髓系细胞的异质性(综述)
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综述主要介绍了Mast、Dendritic、Monocyte、Macrophage、Neutrophils细胞,其中Neutrophils不是很详细,因此只总结了前4中细胞的亚群marker和特征。以思维导图形式总结在幕布,方便以后增删改查。
幕布文档链接: https://www.mubucm.com/doc/7V2nk7N6B_1 密码: 9adx

Mast
marker: TPSAB1, CPA3, KIT, MS4A2
-
high proportion in cancer than normal tissue; -
down-regulate the expression of TNF; -
在不同癌症中其量与预后有正反关系; -
高表达VEGFA促进血管新生 -
表达IL10,TGFB, 招募Treg促进免疫抑制 -
高表达PD-L1 -
释放CCL3、CCL5招募T和NK
Dendritic
Conventional DC (cDC)
cDC1
marker: XCR1, CLEC9A, BATF3, IRF8
-
mainly antitumor
cDC2
marker: CLEC10A, FCER1A, CD1C, CD1E
-
促进Th2、抑制Th17、与CD4+ T互作促进肿瘤 -
activates antitumor CD4+ conventional T cells (Tconvs) in the absence of Treg
Plasmacytoid DC (pDC)
marker: MZB1, LILRA4, IRF7, IL3RA
-
immunosuppressive; -
anti-tumor: release IFNα/β & TNFα
LAMP3+ DC (mregDC)
marker: LAMP3, BIRC3, CCR7, FSCN1
-
high expression of LAMP3, immune regulators [CD274 & FAS], maturation genes (CD40 & CD80) and migratory genes (CCR7 & FSCN1)
2.enriched in intratumor & invasive margin tumor tissues;
-
originate: cDC1 and cDC2,; -
high expression of CCL17, CCL19 & CCL22; -
suppress CD8+ T cells self-renew and function through PD-L1/PD-1 pathway; -
interact with CD8+ T cells from cDC1 ; -
interact with Tregs from cDC2;recuit Treg;
C3
marker: CD88−CD1c+CD163+
-
pro-inflammatory: trigger the expansion of tissue-resident memory CD8+ T cells and enhance MHC expression -
intermediated functional subtype between cDC2 and monocyte, produces TNFα as monocyte & IL23, IL12p70 as cDC2
Monocyte
Classical monocyte
marker: FCN1, CD14, S100A8, VCAN
Nonclassical monocyte
marker: FCN1, FCGR3A, LILRB2, LST1
Intermediate monocyte
marker: FCN1, CD14, FCGR3A
Macrophage
classically activated macrophages (M1)
-
由Toll样受体配体[如脂多糖和干扰素-γ]诱导) -
表达促炎细胞因子和诱导型一氧化氮合酶 -
增强抗肿瘤 Th1 反应并拮抗调节性免疫细胞的抑制活性
alternatively activated macrophages (M2)
-
由IL-4或IL-13诱导 -
表达精氨酸酶1、CD206、CD163、IL-4R、TGF-β1和血小板衍生生长因子(PDGF) -
促进血管生成、肿瘤生长和转移
Monocyte-like macrophages
marker: FCN1, CD163, CD68
FOLR2+ TRM
marker: FOLR2, MRC1
-
enrich: tumor stroma -
prime effector CD8+ T cells -
beneficial to survival
TREM+ recruited macrophages
-
enrichment and activation of T cells and nature killer (NK) cells, which furtherly enhanced ICB therapy
MDSCs-like macrophages
marker: MARCO & TREM1
-
Myeloid-derived suppressor cells
TAM-like macrophage
marker: CD169, CX3CR1, TREM2
-
immature macrophage; -
Enriched in TME with T cells infiltrated or excluded
LYVE1+ TRM
marker: LYVE1, C1QC, PLTP, SEPP1
-
locate: adjacent to blood vessels
NLRP3+ TRM
marker: NLRP3, IL1B, CXCL2, EREG
-
promote the inflammatory response
Alveolar TRM
marker: PPARG, MARCO, MRC1, MSR1
-
canonical TRM
ISG15+ TAM
marker: ISG15, CXCL10, IFITM3, GBP1
C1QC+ TAM
marker: C10A, C1QB, C1QG, APOE
-
phagocytosis and antigen presentation -
originate: FCN1+ monocytes -
locate: adjacent zones
SPP1+ TAM
marker: SPP1, VEGFA, GPNMB, FN1
-
angiogenesis; -
worse prognosis; -
associate with ICB drug resistance -
interact with tumor-specific FAP+ fibroblasts to promote tumor progression -
SPP1+ macrophages and TREM2+ macrophages might largely be overlapped with each other
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