Dept. of Medicine/Gastroenterology; Univ. of Pittsburgh, Pennsylvania 15261, USA.
Am J Physiol Gastrointest Liver Physiol. 2010 Aug;299(2):G531-8. doi: 10.1152/ajpgi.00060.2010. Epub 2010 May 27.
TLR4 ligation by pathogen-associated molecular patterns, such as Gram-negative bacteria-derived LPS, triggers a nonhematopoietic cell-mediated ileus during early endotoxemia. Our objective was to investigate the quantitative contributions of the two downstream signaling pathways of TLR4, namely the adapter proteins myeloid differentiation primary response gene 88 (MyD88) and Toll-IL-1-resistance (TIR) domain-containing adaptor-inducing IFN-beta (TRIF). Six hours after intraperitoneal injection of highly purified LPS (UP-LPS, 5 mg/kg), in vivo gastrointestinal transit and intestinal muscularis gene transcripts of inflammatory mediators chemokine (C-X-C motif) ligand 10, synonymous IP-10 (CXCL10), granulomonocyte colony stimulating factor (GM-CSF, synonymous CSF-2), IL-1beta, IL-6, IL-10, and inducible NO synthase (iNOS) were assessed in mice with transgenic loss-of-function for MyD88 or TRIF. LPS-induced MyD88 and TRIF mRNA upregulation was quantified within the intestinal muscularis of TLR4-competent and TLR4-mutant mice, and MyD88 mRNA levels were additionally measured in TLR4 bone marrow chimeras. MyD88 deficiency completely protected mice from early endotoxin-induced ileus, while TRIF deficiency partially ameliorated ileus severity. LPS induction of the primary downstream signaling element MyD88 was TLR4 dependent and was derived in equal amounts from both the hematopoietic and the nonhematopoietic cells. Conversely, no induction of TRIF mRNA was detectable. Significant gene induction of all inflammatory mediators was dependent on intracellular signal transduction by MyD88, while the TRIF MyD88-independent pathway predominantly regulated the molecular levels of CXCL10. In summary, MyD88 and TRIF are nonredundant signaling pathways in early endotoxin-induced rodent ileus, but MyD88 is the essential adaptor molecule for transduction of early TLR4-induced ileus and inflammatory signaling. The dependency of ileus on individual adaptor protein pathways is also reflected in the manifestation of specific molecular inflammatory events within the intestinal muscularis externa.
TLR4 通过病原体相关分子模式(如革兰氏阴性菌衍生的 LPS)的连接,在早期内毒素血症期间触发非造血细胞介导的肠梗阻。我们的目的是研究 TLR4 的两条下游信号通路的定量贡献,即衔接蛋白髓样分化初级反应基因 88(MyD88)和 Toll-IL-1-抗性(TIR)域包含衔接诱导 IFN-β(TRIF)。腹腔内注射高纯度 LPS(UP-LPS,5mg/kg)6 小时后,在体内胃肠道转运和肠道肌层炎症介质趋化因子(C-X-C 基序)配体 10、同义 IP-10(CXCL10)、粒细胞-巨噬细胞集落刺激因子(GM-CSF,同义 CSF-2)、IL-1β、IL-6、IL-10 和诱导型一氧化氮合酶(iNOS)的基因转录在 MyD88 或 TRIF 转基因功能丧失的小鼠中进行了评估。在 TLR4 功能完整和 TLR4 突变小鼠的肠道肌层中定量了 LPS 诱导的 MyD88 和 TRIF mRNA 的上调,并在 TLR4 骨髓嵌合体中额外测量了 MyD88 mRNA 水平。MyD88 缺陷完全保护小鼠免受早期内毒素诱导的肠梗阻,而 TRIF 缺陷部分改善了肠梗阻的严重程度。LPS 诱导的主要下游信号元件 MyD88 依赖于 TLR4,并且源自造血细胞和非造血细胞的数量相等。相反,无法检测到 TRIF mRNA 的诱导。所有炎症介质的基因诱导均依赖于 MyD88 的细胞内信号转导,而 TRIF MyD88 非依赖性途径主要调节 CXCL10 的分子水平。总之,MyD88 和 TRIF 是早期内毒素诱导的啮齿动物肠梗阻的非冗余信号通路,但 MyD88 是早期 TLR4 诱导的肠梗阻和炎症信号转导的必需衔接分子。肠梗堵对特定衔接蛋白途径的依赖性也反映在肠外膜的特定分子炎症事件的表现中。