1] Ansary Stem Cell Institute, Howard Hughes Medical Institute, Department of Genetic Medicine, Weill Cornell Medical College, New York, New York 10065, USA [2].
Ansary Stem Cell Institute, Howard Hughes Medical Institute, Department of Genetic Medicine, Weill Cornell Medical College, New York, New York 10065, USA.
Nature. 2014 Jan 2;505(7481):97-102. doi: 10.1038/nature12681. Epub 2013 Nov 20.
Chemical or traumatic damage to the liver is frequently associated with aberrant healing (fibrosis) that overrides liver regeneration. The mechanism by which hepatic niche cells differentially modulate regeneration and fibrosis during liver repair remains to be defined. Hepatic vascular niche predominantly represented by liver sinusoidal endothelial cells deploys paracrine trophogens, known as angiocrine factors, to stimulate regeneration. Nevertheless, it is not known how pro-regenerative angiocrine signals from liver sinusoidal endothelial cells is subverted to promote fibrosis. Here, by combining an inducible endothelial-cell-specific mouse gene deletion strategy and complementary models of acute and chronic liver injury, we show that divergent angiocrine signals from liver sinusoidal endothelial cells stimulate regeneration after immediate injury and provoke fibrosis after chronic insult. The pro-fibrotic transition of vascular niche results from differential expression of stromal-derived factor-1 receptors, CXCR7 and CXCR4 (refs 18, 19, 20, 21), in liver sinusoidal endothelial cells. After acute injury, CXCR7 upregulation in liver sinusoidal endothelial cells acts with CXCR4 to induce transcription factor Id1, deploying pro-regenerative angiocrine factors and triggering regeneration. Inducible deletion of Cxcr7 in sinusoidal endothelial cells (Cxcr7(iΔEC/iΔEC)) from the adult mouse liver impaired liver regeneration by diminishing Id1-mediated production of angiocrine factors. By contrast, after chronic injury inflicted by iterative hepatotoxin (carbon tetrachloride) injection and bile duct ligation, constitutive FGFR1 signalling in liver sinusoidal endothelial cells counterbalanced CXCR7-dependent pro-regenerative response and augmented CXCR4 expression. This predominance of CXCR4 over CXCR7 expression shifted angiocrine response of liver sinusoidal endothelial cells, stimulating proliferation of desmin(+) hepatic stellate-like cells and enforcing a pro-fibrotic vascular niche. Endothelial-cell-specific ablation of either Fgfr1 (Fgfr1(iΔEC/iΔEC)) or Cxcr4 (Cxcr4(iΔEC/iΔEC)) in mice restored the pro-regenerative pathway and prevented FGFR1-mediated maladaptive subversion of angiocrine factors. Similarly, selective CXCR7 activation in liver sinusoidal endothelial cells abrogated fibrogenesis. Thus, we demonstrate that in response to liver injury, differential recruitment of pro-regenerative CXCR7-Id1 versus pro-fibrotic FGFR1-CXCR4 angiocrine pathways in vascular niche balances regeneration and fibrosis. These results provide a therapeutic roadmap to achieve hepatic regeneration without provoking fibrosis.
肝脏的化学或创伤性损伤通常与异常愈合(纤维化)有关,这种愈合会破坏肝再生。肝龛细胞如何在肝修复过程中差异调节再生和纤维化的机制仍有待确定。肝血管龛主要由肝窦内皮细胞组成,释放旁分泌营养因子,称为血管生成因子,以刺激再生。然而,尚不清楚肝窦内皮细胞的促再生血管生成信号如何被颠覆以促进纤维化。在这里,我们结合了一种诱导型内皮细胞特异性小鼠基因缺失策略和急性和慢性肝损伤的互补模型,结果表明,肝窦内皮细胞的不同血管生成信号在即时损伤后刺激再生,在慢性损伤后引发纤维化。血管龛的促纤维化转变是由于肝窦内皮细胞中基质衍生因子-1 受体(CXCR7 和 CXCR4)(参考文献 18、19、20、21)的差异表达所致。在急性损伤后,肝窦内皮细胞中 CXCR7 的上调与 CXCR4 一起诱导转录因子 Id1 的表达,从而产生促再生的血管生成因子并触发再生。从成年小鼠肝脏中诱导性删除窦内皮细胞中的 Cxcr7(Cxcr7(iΔEC/iΔEC))会通过减少 Id1 介导的血管生成因子产生来损害肝再生。相比之下,在反复给予肝毒素(四氯化碳)注射和胆管结扎引起的慢性损伤后,肝窦内皮细胞中组成型 FGFR1 信号会抵消 CXCR7 依赖性促再生反应并增加 CXCR4 的表达。这种 CXCR4 对 CXCR7 表达的优势改变了肝窦内皮细胞的血管生成反应,刺激了 desmin(+)肝星状样细胞的增殖,并加强了促纤维化的血管龛。在小鼠中特异性敲除内皮细胞中的 Fgfr1(Fgfr1(iΔEC/iΔEC))或 Cxcr4(Cxcr4(iΔEC/iΔEC))可恢复促再生途径并防止 FGFR1 介导的血管生成因子的适应性颠覆。同样,在肝窦内皮细胞中选择性激活 CXCR7 可消除纤维化。因此,我们证明,在肝损伤后,血管龛中促再生的 CXCR7-Id1 与促纤维化的 FGFR1-CXCR4 血管生成途径的差异募集平衡了再生和纤维化。这些结果为实现肝再生而不引起纤维化提供了治疗路线图。