Department of Molecular and Integrative Physiology, Urbana, IL 61801, USA.
Veterinary Diagnostic Laboratory, Urbana, IL 61801, USA.
Endocrinology. 2022 Jun 1;163(6). doi: 10.1210/endocr/bqac052.
Small heterodimer partner (Shp) regulates several metabolic processes, including bile acid levels, but lacks the conserved DNA binding domain. Phylogenetic analysis revealed conserved genetic evolution of SHP, FXR, CYP7A1, and CYP8B1. Shp, although primarily studied as a downstream target of Farnesoid X Receptor (Fxr), has a distinct hepatic role that is poorly understood. Here, we report that liver-specific Shp knockout (LShpKO) mice have impaired negative feedback of Cyp7a1 and Cyp8b1 on bile acid challenge and demonstrate that a single copy of the Shp gene is sufficient to maintain this response. LShpKO mice also exhibit elevated total bile acid pool with ileal bile acid composition mimicking that of cholic acid-fed control mice. Agonistic activation of Fxr (GW4064) in the LShpKO did not alter the elevated basal expression of Cyp8b1 but lowered Cyp7a1 expression. We found that deletion of Shp led to an enrichment of distinct motifs and pathways associated with circadian rhythm, copper ion transport, and DNA synthesis. We confirmed increased expression of metallothionein genes that can regulate copper levels in the absence of SHP. LShpKO livers also displayed a higher basal proliferation that was exacerbated specifically with bile acid challenge either with cholic acid or 3,5-diethoxycarbonyl-1,4-dihydrocollidine but not with another liver mitogen, 1,4-bis[2-(3,5-dichloropyridyloxy)]benzene. Overall, our data indicate that hepatic SHP uniquely regulates certain proliferative and metabolic cues.
小异二聚体伴侣 (Shp) 调节多种代谢过程,包括胆汁酸水平,但缺乏保守的 DNA 结合域。系统发育分析显示 Shp、FXR、CYP7A1 和 CYP8B1 的遗传进化具有保守性。Shp 主要作为法尼醇 X 受体 (Fxr) 的下游靶标进行研究,但它在肝脏中有独特的作用,目前了解甚少。在这里,我们报告肝特异性 Shp 敲除 (LShpKO) 小鼠对胆汁酸挑战的 Cyp7a1 和 Cyp8b1 的负反馈受损,并证明 Shp 基因的一个拷贝足以维持这种反应。LShpKO 小鼠还表现出升高的总胆汁酸池,回肠胆汁酸组成类似于胆酸喂养对照小鼠。在 LShpKO 中激动性激活 Fxr (GW4064) 不会改变 Cyp8b1 的升高基础表达,但会降低 Cyp7a1 的表达。我们发现 Shp 的缺失导致与昼夜节律、铜离子转运和 DNA 合成相关的独特基序和途径富集。我们证实了金属硫蛋白基因的表达增加,这些基因可以在没有 SHP 的情况下调节铜水平。LShpKO 肝脏还表现出更高的基础增殖,在胆酸或 3,5-二乙氧羰基-1,4-二氢-collidine 的情况下,特别是在胆汁酸挑战时,这种增殖会加剧,但在另一种肝有丝分裂原 1,4-双[2-(3,5-二氯吡啶氧基)]苯时则不会。总的来说,我们的数据表明肝 Shp 独特地调节某些增殖和代谢线索。