RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Cutting Edge: PDGF-DD Binding to NKp44 Costimulates TLR9 Signaling and Proinflammatory Cytokine Secretion in Human Plasmacytoid Dendritic Cells.
Cutting Edge: PDGF-DD Binding to NKp44 Costimulates TLR9 Signaling and Proinflammatory Cytokine Secretion in Human Plasmacytoid Dendritic Cells.
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NKp44是一种人类受体,最初发现于活化的NK细胞、1型及3型固有淋巴样细胞上,可结合血小板衍生生长因子D(PDGF-DD)二聚体。NKp44也表达于组织浆细胞样树突状细胞(PDCs),但PDCs上NKp44与PDGF-DD的相互作用尚未被研究。在体外,NKp44与PDGF-DD的结合增强了PDC在TLR9配体CpG-ODN刺激下分泌IFN-α、TNF和IL-6,但对TLR7/8配体无此效应。在组织中,PDCs与表达PDGF-DD的细胞密切接触,见于扁桃体、黑色素瘤和传染性软疣感染皮肤病变的高内皮微静脉和上皮。重组PDGF-DD增强了人源化小鼠模型中对系统性HSV-1感染的血清IFN-α应答。
我们得出结论:NKp44与TLR9信号整合以增强PDC细胞因子产生。这些发现可能对基于TLR9的佐剂免疫应答、表达PDGF-DD的肿瘤治疗,以及诱导PDGF-DD表达以增强病毒传播的DNA病毒感染具有重要意义。
NKp44 is a human receptor originally found on activated NK cells, group 1 and group 3 innate lymphoid cells that binds dimers of platelet-derived growth factor D (PDGF-DD). NKp44 is also expressed on tissue plasmacytoid dendritic cells (PDCs), but NKp44-PDGF-DD interaction on PDCs remains unstudied. Engagement of NKp44 with PDGF-DD in vitro enhanced PDC secretion of IFN-α, TNF, and IL-6 in response to the TLR9 ligand CpG-ODN, but not TLR7/8 ligands.
In tissues, PDCs were found in close contact with PDGF-DD-expressing cells in the high endothelial venules and epithelium of tonsils, melanomas, and skin lesions infected with Molluscum contagiosum. Recombinant PDGF-DD enhanced the serum IFN-α response to systemic HSV-1 infection in a humanized mouse model.
We conclude that NKp44 integrates with TLR9 signaling to enhance PDC cytokine production.
These findings may have bearings for immune responses to TLR9-based adjuvants, therapy for tumors expressing PDGF-DD, and infections with DNA viruses that induce PDGF-DD expression to enhance viral spread.
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