中文摘要：

最近的數(shù)據(jù)表明，即使在肝硬化的后期，肝纖維化也可以消退，將免疫反應(yīng)從促炎性轉(zhuǎn)變?yōu)榭苫謴?fù)性譜被認(rèn)為是一個(gè)有前途的選擇置之不顧。控制炎癥表型變化并因此可能逆轉(zhuǎn)肝纖維化的免疫調(diào)節(jié)網(wǎng)絡(luò)鮮為人知實力增強。在這里選擇適用，我們表明橋梁作用，在從終末期纖維化患者獲得的精確切割的人肝切片和小鼠模型中問題分析，使用藥物或抗體驅(qū)動(dòng)的方法抑制粘膜相關(guān)不變 T細(xì)胞 （MAIT） 培養，限制纖維化進(jìn)展交流研討，甚至消退纖維化更加完善，在慢性毒性或非酒精性脂肪性肝炎 （NASH） 誘導(dǎo)的肝損傷后。結(jié)合 RNA 測(cè)序建設應用、體內(nèi)功能研究（在雄性小鼠中進(jìn)行）和共培養(yǎng)實(shí)驗(yàn)的機(jī)制研究表明支撐作用，MAIT 細(xì)胞-單核細(xì)胞/巨噬細(xì)胞相互作用的破壞通過增加恢復(fù)性 Ly6C^lo 的比率而犧牲促纖維化 Ly6C^hi 單核細(xì)胞衍生的巨噬細(xì)胞并促進(jìn)兩個(gè)亞群中的自噬表型日漸深入。因此，我們的數(shù)據(jù)表明同時，MAIT 細(xì)胞活化和肝臟巨噬細(xì)胞隨之而來的表型轉(zhuǎn)變是肝纖維化的重要致病特征互動式宣講，可以靶向抗纖維化治療。

英文摘要：

Recent data have shown that liver fibrosis can regress even at later stages of cirrhosis and shifting the immune response from pro-inflammatory towards a resolutive profile is considered as a promising option. The immune regulatory networks that govern the shift of the inflammatory phenotype and thus potential reversal of liver fibrosis are lesser known. Here we show that in precision-cut human liver slices obtained from patients with end-stage fibrosis and in mouse models, inhibiting Mucosal-Associated Invariant T (MAIT) cells using pharmacological or antibody-driven approaches, limits fibrosis progression and even regresses fibrosis, following chronic toxic- or non-alcoholic steatohepatitis (NASH)-induced liver injury. Mechanistic studies, combining RNA sequencing, in vivo functional studies (performed in male mice) and co-culture experiments indicate that disruption of the MAIT cell-monocyte/macrophage interaction results in resolution of fibrosis both by increasing the frequency of restorative Ly6C^lo at the expenses of pro-fibrogenic Ly6C^hi monocyte-derived macrophages and promoting an autophagic phenotype in both subsets. Thus, our data show that MAIT cell activation and the consequential phenotype shift of liver macrophages are important pathogenic features of liver fibrosis and could be targeted by anti-fibrogenic therapy.

論文信息：

論文題目：MAIT cell inhibition promotes liver fibrosis regression via macrophage phenotype reprogramming

期刊名稱：Nature Communications

時(shí)間期卷：14, Article number: 1830 (2023)

在線時(shí)間：2023年4月1日

DOI：doi.org/10.1038/s41467-023-37453-5

產(chǎn)品信息：

貨號(hào)：CP-005-005

規(guī)格：5ml+5ml

品牌：Liposoma

產(chǎn)地：荷蘭

名稱：Clodronate Liposomes and Control Liposomes

辦事處：Target Technology（靶點(diǎn)科技）

Clodronate Liposomes氯膦酸鹽脂質(zhì)體助力肝臟纖維化模型研究模式，荷蘭Liposoma巨噬細(xì)胞清除劑Clodronate Liposomes見刊于Nature Communications：

氯膦酸二鈉脂質(zhì)體清除肝臟巨噬細(xì)胞助力肝纖維化恢復(fù)研究

Liposoma巨噬細(xì)胞清除劑Clodronate Liposomes氯膦酸二鈉脂質(zhì)體的材料和方法：

Macrophage depletion by clodronate liposomes

To deplete macrophages, C57BL/6?J mice with established fibrosis were given one i.v injection of liposome-encapsulated clodronate (Clodronate Liposomes, 0.1?ml/10?g, B#C23J0518, Liposoma). Liposome-encapsulated PBS was used as control (B#P24J0518, Liposoma). Ac-6-FP was then administered daily until the sacrifice at day 1, day 2, or day 4 following the last CCl4 injection. Timeline of injections shown in Fig. 3g（見下圖） were created with BioRender® software.