Pharmacology & Therapeutics, Journal Year: 2020, Volume and Issue: 222, P. 107791 - 107791
Published: Dec. 13, 2020
Language: Английский
Pharmacology & Therapeutics, Journal Year: 2020, Volume and Issue: 222, P. 107791 - 107791
Published: Dec. 13, 2020
Language: Английский
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
521PROTEOMICS, 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
170Computational 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
152Nutrients, 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
101International 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
89International 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
69Molecular and Cellular Endocrinology, Journal Year: 2019, Volume and Issue: 502, P. 110665 - 110665
Published: Nov. 21, 2019
Language: Английский
Citations
140Acta 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
93Journal 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
88Journal 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