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文獻閱讀003:單細胞腫瘤浸潤性髓系細胞的異質性(綜述)

綜述主要介紹了Mast、Dendritic、Monocyte、Macrophage、Neutrophils細胞,其中Neutrophils不是很詳細,因此只總結了前4中細胞的亞群marker和特征。以思維導圖形式總結在幕布,方便以后增刪改查。

幕布文檔鏈接: https://www.mubucm.com/doc/7V2nk7N6B_1 密碼: 9adx

Mast

marker: TPSAB1, CPA3, KIT, MS4A2

  1. high proportion in cancer than normal tissue;
  2. down-regulate the expression of TNF;
  3. 在不同癌癥中其量與預后有正反關系;
  4. 高表達VEGFA促進血管新生
  5. 表達IL10,TGFB, 招募Treg促進免疫抑制
  6. 高表達PD-L1
  7. 釋放CCL3、CCL5招募T和NK

Dendritic

Conventional DC (cDC)

cDC1

marker: XCR1, CLEC9A, BATF3, IRF8

  1. mainly antitumor

cDC2

marker: CLEC10A, FCER1A, CD1C, CD1E

  1. 促進Th2、抑制Th17、與CD4+ T互作促進腫瘤
  2. activates antitumor CD4+ conventional T cells (Tconvs) in the absence of Treg

Plasmacytoid DC (pDC)

marker: MZB1, LILRA4, IRF7, IL3RA

  1. immunosuppressive;
  2. anti-tumor: release IFNα/β & TNFα

LAMP3+ DC (mregDC)

marker: LAMP3, BIRC3, CCR7, FSCN1

  1. 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;

  1. originate: cDC1 and cDC2,;
  2. high expression of CCL17, CCL19 & CCL22;
  3. suppress CD8+ T cells self-renew and function through PD-L1/PD-1 pathway;
  4. interact with CD8+ T cells from cDC1 ;
  5. interact with Tregs from cDC2;recuit Treg;

C3

marker: CD88?CD1c+CD163+

  1. pro-inflammatory: trigger the expansion of tissue-resident memory CD8+ T cells and enhance MHC expression
  2. 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)

  1. 由Toll樣受體配體[如脂多糖和干擾素-γ]誘導)
  2. 表達促炎細胞因子和誘導型一氧化氮合酶
  3. 增強抗腫瘤 Th1 反應并拮抗調節(jié)性免疫細胞的抑制活性

alternatively activated macrophages (M2)

  1. 由IL-4或IL-13誘導
  2. 表達精氨酸酶1、CD206、CD163、IL-4R、TGF-β1和血小板衍生生長因子(PDGF)
  3. 促進血管生成、腫瘤生長和轉移

Monocyte-like macrophages

marker: FCN1, CD163, CD68

FOLR2+ TRM

marker: FOLR2, MRC1

  1. enrich: tumor stroma
  2. prime effector CD8+ T cells
  3. beneficial to survival

TREM+ recruited macrophages

  1. enrichment and activation of T cells and nature killer (NK) cells, which furtherly enhanced ICB therapy

MDSCs-like macrophages

marker: MARCO  & TREM1

  1. Myeloid-derived suppressor cells

TAM-like macrophage

marker: CD169, CX3CR1, TREM2

  1. immature macrophage;
  2. Enriched in TME with T cells infiltrated or excluded

LYVE1+ TRM

marker: LYVE1, C1QC, PLTP, SEPP1

  1. locate: adjacent to blood vessels

NLRP3+ TRM

marker: NLRP3, IL1B, CXCL2, EREG

  1. promote the inflammatory response

Alveolar TRM

marker: PPARG, MARCO, MRC1, MSR1

  1. canonical TRM

ISG15+ TAM

marker: ISG15, CXCL10, IFITM3, GBP1

C1QC+ TAM

marker: C10A, C1QB, C1QG, APOE

  1. phagocytosis and antigen presentation
  2. originate: FCN1+ monocytes
  3. locate: adjacent zones

SPP1+ TAM

marker: SPP1, VEGFA, GPNMB, FN1

  1. angiogenesis;
  2. worse prognosis;
  3. associate with ICB drug resistance
  4. interact with tumor-specific FAP+ fibroblasts to promote tumor progression
  5. SPP1+ macrophages and TREM2+ macrophages might largely be overlapped with each other
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