Peroxisome proliferator-activated receptors in the pathogenesis and therapies of liver fibrosis DOI
Xin Han, Yan‐Ling Wu, Qiao Yang

et al.

Pharmacology & Therapeutics, Journal Year: 2020, Volume and Issue: 222, P. 107791 - 107791

Published: Dec. 13, 2020

Language: Английский

An update on the regulatory mechanisms of NLRP3 inflammasome activation DOI Creative Commons
Seungwha Paik, Jin Kyung Kim, Prashanta Silwal

et al.

Cellular and Molecular Immunology, Journal Year: 2021, Volume and Issue: 18(5), P. 1141 - 1160

Published: April 13, 2021

Abstract The NOD-, LRR-, and pyrin domain-containing protein 3 (NLRP3) inflammasome is a multiprotein complex involved in the release of mature interleukin-1β triggering pyroptosis, which paramount importance variety physiological pathological conditions. Over past decade, considerable advances have been made elucidating molecular mechanisms underlying priming/licensing (Signal 1) assembly 2) NLRP3 activation. Recently, number studies indicated that step regulated by complicated at both transcriptional posttranslational levels. In this review, we discuss current understanding mechanistic details activation with particular emphasis on protein-protein interactions, modifications, spatiotemporal regulation machinery. We also present detailed summary multiple positive and/or negative regulatory pathways providing upstream signals culminate assembly. A better will provide opportunities for development methods prevention treatment inflammasome-related diseases.

Language: Английский

Citations

521

Transcription factors: Bridge between cell signaling and gene regulation DOI Creative Commons
Paula Weidemüller, Maksim Kholmatov, Evangelia Petsalaki

et al.

PROTEOMICS, Journal Year: 2021, Volume and Issue: 21(23-24)

Published: July 27, 2021

Transcription factors (TFs) are key regulators of intrinsic cellular processes, such as differentiation and development, the response to external perturbation through signaling pathways. In this review we focus on role TFs a link between pathways gene regulation. Cell tends result in modulation set that then lead changes cell's transcriptional program. We highlight molecular layers at which TF activity can be measured associated technical conceptual challenges. These include post-translational modifications (PTMs) TF, regulation binding DNA chromatin accessibility epigenetics, expression target genes. large number understudied both studies, our knowledge about known targets has strong literature bias. argue serve perfect bridge fields signaling, separating these hinders understanding cell functions. Multi-omics approaches measure multiple dimensions ideally suited study interplay using anchor two fields.

Language: Английский

Citations

170

Farnesoid X receptor (FXR): Structures and ligands DOI Creative Commons
Longying Jiang, Huajun Zhang, Desheng Xiao

et al.

Computational and Structural Biotechnology Journal, Journal Year: 2021, Volume and Issue: 19, P. 2148 - 2159

Published: Jan. 1, 2021

Farnesoid X receptor (FXR) is a bile acid activated nuclear (BAR) and mainly expressed in the liver intestine. Upon ligand binding, FXR regulates key genes involved metabolic process of synthesis, transport reabsorption also metabolism carbohydrates lipids. Because its important functions, considered as promising drug target for therapy acid-related diseases. With approval obeticholic (OCA) first small molecule to FXR, many other molecules are being evaluated clinical trials. This review summarizes structures especially binding domain, development (including agonists antagonists) targeting FXR.

Language: Английский

Citations

152

Vitamin D and Its Target Genes DOI Open Access
Carsten Carlberg

Nutrients, Journal Year: 2022, Volume and Issue: 14(7), P. 1354 - 1354

Published: March 24, 2022

The vitamin D metabolite 1α,25-dihydroxyvitamin D3 is the natural, high-affinity ligand of transcription factor receptor (VDR). In many tissues and cell types, VDR binds in a ligand-dependent fashion to thousands genomic loci modulates, via local chromatin changes, expression hundreds primary target genes. Thus, epigenome transcriptome VDR-expressing cells directly affected by D. Vitamin genes encode for proteins with large variety physiological functions, ranging from control calcium homeostasis, innate adaptive immunity, cellular differentiation. This review will discuss VDR’s binding DNA, as well its genome-wide locations interaction partner proteins, context chromatin. information be integrated into model signaling, explaining regulation

Language: Английский

Citations

101

Molecular Basis of Bile Acid-FXR-FGF15/19 Signaling Axis DOI Open Access

Takeshi Katafuchi,

Makoto Makishima

International Journal of Molecular Sciences, Journal Year: 2022, Volume and Issue: 23(11), P. 6046 - 6046

Published: May 27, 2022

Bile acids (BAs) are a group of amphiphilic molecules consisting rigid steroid core attached to hydroxyl with varying number, position, and orientation, hydrophilic side chain. While BAs act as detergents solubilize lipophilic nutrients in the small intestine during digestion absorption, they also hormones. Farnesoid X receptor (FXR) is nuclear that forms heterodimer retinoid α (RXRα), activated by enterohepatic circulation reabsorbed via transporters ileum colon, plays critical role regulating gene expression involved cholesterol, BA, lipid metabolism liver. The FXR/RXRα exists distal regulates production fibroblast growth factor (FGF) 15/FGF19, hormone traveling activates hepatic FGF 4 (FGFR4)-β-klotho complex metabolism, well those cell proliferation. Agonists for FXR analogs FGF15/19 currently recognized promising therapeutic target metabolic syndrome cholestatic diseases.

Language: Английский

Citations

89

Roles of Estrogen, Estrogen Receptors, and Estrogen-Related Receptors in Skeletal Muscle: Regulation of Mitochondrial Function DOI Open Access
Kenta Yoh, Kazuhiro Ikeda,

Kuniko Horie

et al.

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(3), P. 1853 - 1853

Published: Jan. 17, 2023

Estrogen is an essential sex steroid hormone that functions primarily in female reproductive system, as well a variety of tissues and organs with pleiotropic effects, such cardiovascular, nervous, immune, musculoskeletal systems. Women low estrogen, exemplified by those postmenopause, are therefore prone to suffer from various disorders, i.e., cardiovascular disease, dementia, metabolic syndrome, osteoporosis, sarcopenia, frailty, so on. regulates the expression its target genes binding cognate receptors, estrogen receptors (ERs) α β. Notably, estrogen-related (ERRs) α, β, γ originally identified orphan share substantial structural homology common transcriptional targets ERs. Accumulating evidence suggests ERs ERRs play crucial roles skeletal muscles, muscle mass maintenance, exercise physiology, regeneration. In this article, we review potential regulatory particularly regard mitochondrial function metabolism.

Language: Английский

Citations

69

Nuclear receptors are the major targets of endocrine disrupting chemicals DOI Creative Commons

Lucia Toporová,

Patrick Balaguer

Molecular and Cellular Endocrinology, Journal Year: 2019, Volume and Issue: 502, P. 110665 - 110665

Published: Nov. 21, 2019

Language: Английский

Citations

140

Targeting autophagy using small-molecule compounds to improve potential therapy of Parkinson's disease DOI Creative Commons
Kai Zhang, Shiou Zhu, Jiamei Li

et al.

Acta Pharmaceutica Sinica B, Journal Year: 2021, Volume and Issue: 11(10), P. 3015 - 3034

Published: Feb. 26, 2021

Parkinson's disease (PD), known as one of the most universal neurodegenerative diseases, is a serious threat to health elderly. The current treatment has been demonstrated relieve symptoms, and discovery new small-molecule compounds regarded promising strategy. Of note, homeostasis autolysosome pathway (ALP) closely associated with PD, impaired autophagy may cause death neurons thereby accelerating progress PD. Thus, pharmacological targeting drawn rising attention so far. In this review, we focus on summarizing several autophagy-associated targets, such AMPK, mTORC1, ULK1, IMPase, LRRK2, beclin-1, TFEB, GCase, ERRα, C-Abelson, well their relevant in PD models, which will shed light clue exploiting more potential targeted drugs tracking near future.

Language: Английский

Citations

93

Xenobiotic metabolism and transport in Caenorhabditis elegans DOI Creative Commons
Jessica H. Hartman, Samuel J. Widmayer, Christina M. Bergemann

et al.

Journal of Toxicology and Environmental Health Part B, Journal Year: 2021, Volume and Issue: 24(2), P. 51 - 94

Published: Feb. 17, 2021

Caenorhabditis elegans has emerged as a major model in biomedical and environmental toxicology. Numerous papers on toxicology pharmacology C. have been published, this species now adopted by investigators academic toxicology, pharmacology, drug discovery labs. also attracted the interest of governmental regulatory agencies charged with evaluating safety chemicals. However, major, fundamental aspect toxicological science remains underdeveloped elegans: xenobiotic metabolism transport processes that are critical to understanding toxicokinetics toxicodynamics, extrapolation other species. The aim review was initially briefly describe history trajectory use pharmacological studies. Subsequently, physical barriers chemical uptake role worm microbiome transformation were described. Then what is not known regarding classic Phase I, II, III performed. In addition, following discussed (1) regulation metabolism; (2) published for specific chemicals; (3) genetic diversity these elegans. Finally, placed an evolutionary context; key areas future research highlighted; implications extrapolating toxicity results discussed.

Language: Английский

Citations

88

Bilirubin remodels murine white adipose tissue by reshaping mitochondrial activity and the coregulator profile of peroxisome proliferator–activated receptor α DOI Creative Commons
Darren M. Gordon, Kari L. Neifer, Abdul‐rizaq Hamoud

et al.

Journal of Biological Chemistry, Journal Year: 2020, Volume and Issue: 295(29), P. 9804 - 9822

Published: May 14, 2020

Activation of lipid-burning pathways in the fat-storing white adipose tissue (WAT) is a promising strategy to improve metabolic health and reduce obesity, insulin resistance, type II diabetes. For unknown reasons, bilirubin levels are negatively associated with obesity Here, using mice an array approaches, including MRI assess body composition, biochemical assays measure fatty acids, MitoTracker-based mitochondrial analysis, immunofluorescence, high-throughput coregulator we show that functions as molecular switch for nuclear receptor transcription factor peroxisome proliferator-activated α (PPARα). Bilirubin exerted its effects by recruiting dissociating specific coregulators WAT, driving expression PPARα target genes such uncoupling protein 1 (Ucp1) adrenoreceptor β 3 (Adrb3). We also found selective ligand does not affect activities related proteins PPARγ PPARδ. further diet-induced obese mild hyperbilirubinemia have reduced WAT size increased number mitochondria, restructuring PPARα-binding coregulators. conclude strongly affects organismal weight reshaping profile, remodeling function, reducing fat accumulation.

Language: Английский

Citations

78