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Macrophage Dicer promotes tolerogenic apoptotic cell clearance and immune tolerance by inhibiting pentose phosphate pathway activity

机译:通过抑制戊糖磷酸途径活性巨噬细胞DICER促进耐受性凋亡细胞间隙和免疫耐受性

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摘要

Dicer regulates immune-silent clearance of ACs and immune tolerance by inhibiting pentose phosphate pathway activity in macrophages. A In vitro cultured WT, Dicer1-C or Dicer1-CKO mouse peritoneal macrophages were incubated with pHrodo-labeled apoptotic thymocytes for the indicated times, and phagocytosis was analyzed by flow cytometry (n = 3). B Dexamethasone (Dex, 0.2 mg) was i.p. injected into 4-week-old WT or Dicer1-CKO mice, and after 24 h, the numbers of Annexin V+ apoptotic cells and CD68+ macrophages were analyzed by flow cytometry (n = 3). C In vitro cultured WT or Dicer1-CKO mouse peritoneal macrophages were incubated with apoptotic thymocytes for 24 h, and the mRNA expression of inflammatory cytokines in macrophages was measured by quantitative RT-PCR (n = 3). D–F In vitro cultured WT or Dicer1-CKO mouse peritoneal macrophages were incubated with apoptotic human Jurkat T cells for 6 h, and macrophage transcriptional profiles were assessed by mRNA sequencing (D, En = 3) or quantitative RT-PCR (F, n = 3). D KEGG enrichment plot of the pentose phosphate pathway (KO00030), as determined by Gene Set Enrichment Analysis (GSEA). E The expression of enriched genes in the pentose phosphate pathway, as determined by GSEA. F Validation of enriched genes in the pentose phosphate pathway by quantitative RT-PCR. G In vitro cultured WT or Dicer1-CKO mouse peritoneal macrophages were incubated with DHEA (1 μM), 6-AN (10 μM) or PBS for 24 h, and the phagocytosis of pHrodo-labeled apoptotic thymocytes was measured by flow cytometry (n = 3). H Serum concentrations of anti-dsDNA antibodies (ADAs) and anti-nuclear antibodies (ANAs) in WT and Dicer1-CKO mice of different ages were analyzed by ELISA (n = 6). I IgG and C3 levels in the kidneys of 60-week-old WT and Dicer1-CKO mice (n = 3, bar = 100 μm). J Kidney functions in 60-week-old WT and Dicer1-CKO mice (n = 6). K Schematic diagram of the role of macrophage Dicer in apoptotic cell clearance and immune tolerance. The results are expressed as the mean ± SEM, n.s. not statistically significant, *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001, two-tailed Student’s t test for two groups (B, C, F, J), one-way (B, G, H) or two-way (A) ANOVA with Tukey’s post hoc test for multiple groups
机译:通过抑制巨噬细胞的戊糖磷酸盐途径活性,调节对ACS和免疫耐受的免疫静音清除。将一种体外培养的WT,Dicer1-C或Dicer1-CKO小鼠腹膜巨噬细胞与表明时间的前型凋亡胸腺细胞一起培养,通过流式细胞术分析吞噬作用(n = 3)。 B dexamethasone(dex,0.2mg)是i.p.注射到4周龄WT或DICER1-CKO小鼠中,并在24小时后,通过流式细胞术分析膜蛋白v +凋亡细胞和CD68 +巨噬细胞的数量(n = 3)。 C体外培养的WT或DICER1-CKO小鼠腹膜巨噬细胞与凋亡胸腺细胞孵育24小时,并通过定量RT-PCR测量巨噬细胞中炎性细胞因子的mRNA表达(n = 3)。将D-F在体外培养的WT或DICER1-CKO小鼠腹膜巨噬细胞与凋亡人Jurkat T细胞一起孵育6小时,并通过mRNA测序评估巨噬细胞转录谱(D,E.n = 3)或定量RT-PCR(F,N = 3)。 D甘蔗磷酸盐途径(KO00030)的D Gegg浓缩图,如基因设定富集分析(GSEA)所确定的。 e通过GSEA确定的磷酸磷途径中富集基因的表达。 F通过定量RT-PCR验证戊磷酸磷途径中的富集基因。克体外培养WT或DICER1-CKO小鼠腹腔巨噬细胞用DHEA(1μM),6-AN(10μM)或PBS孵育24小时,和的pHrodo标记凋亡细胞的吞噬作用,通过流式细胞术(n个测量= 3)。通过ELISA(n = 6)分析WT和Dicer1-CKO小鼠中的抗DSDNA抗体(ADAS)和抗核抗体(ANAS)的H血清浓度(n = 6)。 IgG和Dicer1-CKO小鼠肾脏的IgG和C3水平(n = 3,棒=100μm)。 J肾功能在60周龄WT和Dicer1-CKO小鼠中(n = 6)。 K巨噬细胞Dicer在凋亡细胞间隙和免疫耐受的原理图。结果表示为平均值±SEM,N.S.没有统计学意义,* P <0.05; ** p <0.01; *** p <0.001; **** P <0.0001,双尾学生的T测试两组(B,C,F,J),单向(B,G,H)或双向(A)ANOVA,具有Tukey HOC测试对于多个组

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