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磷脂酰肌醇-4,5-二磷酸 3-激酶 δ 同工酶在肝细胞增殖中的新作用。

A Novel Role for the Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Delta Isoform in Hepatocellular Proliferation.

机构信息

Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania.

Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania.

出版信息

Am J Pathol. 2024 Aug;194(8):1511-1527. doi: 10.1016/j.ajpath.2024.03.016. Epub 2024 May 3.

Abstract

The phosphatidylinositol-4,5-bisphosphate 3-kinase delta isoform (Pik3cd), usually considered immune-specific, was unexpectedly identified as a gene potentially related to either regeneration and/or differentiation in animals lacking hepatocellular Integrin Linked Kinase (ILK). Since a specific inhibitor (Idelalisib, or CAL101) for the catalytic subunit encoded by Pik3cd (p110δ) has reported hepatotoxicity when used for treating chronic lymphocytic leukemia and other lymphomas, the authors aimed to elucidate whether there is a role for p110δ in normal liver function. To determine the effect on normal liver regeneration, partial hepatectomy (PHx) was performed using mice in which p110δ was first inhibited using CAL101. Inhibition led to over a 50% decrease in proliferating hepatocytes in the first 2 days after PHx. This difference correlated with phosphorylation changes in the HGF and EGF receptors (MET and EGFR, respectively) and NF-κB signaling. Ingenuity Pathway Analyses implicated C/EBPβ, HGF, and the EGFR heterodimeric partner, ERBB2, as three of the top 20 regulators downstream of p110δ signaling because their pathways were suppressed in the presence of CAL101 at 1 day post-PHx. A regulatory role for p110δ signaling in mouse and rat hepatocytes through MET and EGFR was further verified using hepatocyte primary cultures, in the presence or absence of CAL101. Combined, these data support a role for p110δ as a downstream regulator of normal hepatocytes when stimulated to proliferate.

摘要

磷脂酰肌醇-4,5-二磷酸 3-激酶 δ 同工型(Pik3cd)通常被认为是免疫特异性的,但在缺乏肝细胞整合素连接激酶(ILK)的动物中,出乎意料地被鉴定为与再生和/或分化相关的潜在基因。由于针对编码 Pik3cd(p110δ)的催化亚基的特异性抑制剂(idelalisib 或 CAL101)在用于治疗慢性淋巴细胞白血病和其他淋巴瘤时已报道有肝毒性,作者旨在阐明 p110δ 在正常肝功能中的作用。为了确定对正常肝再生的影响,使用首先使用 CAL101 抑制 p110δ 的小鼠进行部分肝切除术(PHx)。抑制导致 PHx 后前两天增殖肝细胞减少超过 50%。这种差异与 HGF 和 EGF 受体(MET 和 EGFR)和 NF-κB 信号转导的磷酸化变化相关。Ingenuity Pathway Analyses 表明 C/EBPβ、HGF 和 EGFR 异二聚体伴侣 ERBB2 是 p110δ 信号下游的前 20 个调节剂中的三个,因为在 PHx 后 1 天存在 CAL101 时,它们的途径被抑制。在存在或不存在 CAL101 的情况下,使用肝细胞原代培养物进一步验证了 p110δ 信号通过 MET 和 EGFR 在小鼠和大鼠肝细胞中的调节作用。综上所述,这些数据支持了 p110δ 在受到刺激增殖的正常肝细胞中作为下游调节剂的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a64/11393825/3b89b60d77fa/gr1.jpg

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