Studer P, da Silva C G, Revuelta Cervantes J M, Mele A, Csizmadia E, Siracuse J J, Damrauer S M, Peterson C R, Candinas D, Stroka D M, Ma A, Bhasin M, Ferran C
Division of Vascular Surgery, Center for Vascular biology Research and the Transplant Institute, Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Department of Visceral Surgery and Medicine, University Hospital Bern, Bern, Switzerland.
Cell Death Differ. 2015 Dec;22(12):2068-77. doi: 10.1038/cdd.2015.52. Epub 2015 May 15.
Hepatic expression of A20, including in hepatocytes, increases in response to injury, inflammation and resection. This increase likely serves a hepatoprotective purpose. The characteristic unfettered liver inflammation and necrosis in A20 knockout mice established physiologic upregulation of A20 as integral to the anti-inflammatory and anti-apoptotic armamentarium of hepatocytes. However, the implication of physiologic upregulation of A20 in modulating hepatocytes' proliferative responses following liver resection remains controversial. To resolve the impact of A20 on hepatocyte proliferation and the liver's regenerative capacity, we examined whether decreased A20 expression, as in A20 heterozygous knockout mice, affects outcome following two-third partial hepatectomy. A20 heterozygous mice do not demonstrate a striking liver phenotype, indicating that their A20 expression levels are still sufficient to contain inflammation and cell death at baseline. However, usually benign partial hepatectomy provoked a staggering lethality (>40%) in these mice, uncovering an unsuspected phenotype. Heightened lethality in A20 heterozygous mice following partial hepatectomy resulted from impaired hepatocyte proliferation due to heightened levels of cyclin-dependent kinase inhibitor, p21, and deficient upregulation of cyclins D1, E and A, in the context of worsened liver steatosis. A20 heterozygous knockout minimally affected baseline liver transcriptome, mostly circadian rhythm genes. Nevertheless, this caused differential expression of >1000 genes post hepatectomy, hindering lipid metabolism, bile acid biosynthesis, insulin signaling and cell cycle, all critical cellular processes for liver regeneration. These results demonstrate that mere reduction of A20 levels causes worse outcome post hepatectomy than full knockout of bona fide liver pro-regenerative players such as IL-6, clearly ascertaining A20's primordial role in enabling liver regeneration. Clinical implications of these data are of utmost importance as they caution safety of extensive hepatectomy for donation or tumor in carriers of A20/TNFAIP3 single nucleotide polymorphisms alleles that decrease A20 expression or function, and prompt the development of A20-based liver pro-regenerative therapies.
A20在肝脏中的表达,包括在肝细胞中的表达,会随着损伤、炎症和切除而增加。这种增加可能具有肝脏保护作用。A20基因敲除小鼠中典型的不受控制的肝脏炎症和坏死,确立了A20的生理性上调是肝细胞抗炎和抗凋亡机制的组成部分。然而,A20的生理性上调在调节肝切除术后肝细胞增殖反应中的意义仍存在争议。为了阐明A20对肝细胞增殖和肝脏再生能力的影响,我们研究了A20杂合基因敲除小鼠中A20表达降低是否会影响三分之二部分肝切除术后的结果。A20杂合小鼠没有表现出明显的肝脏表型,这表明它们的A20表达水平在基线时仍足以控制炎症和细胞死亡。然而,通常良性的部分肝切除术在这些小鼠中引发了惊人的致死率(>40%),揭示了一种未被怀疑的表型。部分肝切除术后A20杂合小鼠的致死率升高是由于细胞周期蛋白依赖性激酶抑制剂p21水平升高导致肝细胞增殖受损,以及在肝脂肪变性加重的情况下,细胞周期蛋白D1、E和A的上调不足。A20杂合基因敲除对基线肝脏转录组的影响最小,主要是昼夜节律基因。尽管如此,这导致肝切除术后1000多个基因的差异表达,阻碍了脂质代谢、胆汁酸生物合成、胰岛素信号传导和细胞周期,而这些都是肝脏再生的关键细胞过程。这些结果表明,仅仅降低A20水平会导致肝切除术后的结果比完全敲除真正的肝脏促再生因子(如IL-6)更差,这清楚地确定了A20在促进肝脏再生中的首要作用。这些数据的临床意义至关重要,因为它们提醒人们,对于携带降低A20表达或功能的A20/TNFAIP3单核苷酸多态性等位基因的供体或肿瘤患者,广泛肝切除术的安全性,并促使开发基于A20的肝脏促再生疗法。