Dianxin Liu

ORCID: 0000-0003-2282-7386
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About
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Research Areas
  • Adipose Tissue and Metabolism
  • Adipokines, Inflammation, and Metabolic Diseases
  • Receptor Mechanisms and Signaling
  • Hormonal Regulation and Hypertension
  • Estrogen and related hormone effects
  • Heart Failure Treatment and Management
  • Sirtuins and Resveratrol in Medicine
  • Genomics, phytochemicals, and oxidative stress
  • Pancreatic function and diabetes
  • Diet and metabolism studies
  • Muscle metabolism and nutrition
  • Glycosylation and Glycoproteins Research
  • Pain Mechanisms and Treatments
  • Diabetes Treatment and Management
  • Metabolism, Diabetes, and Cancer
  • Biochemical Analysis and Sensing Techniques
  • Neuropeptides and Animal Physiology
  • GDF15 and Related Biomarkers
  • Cancer, Stress, Anesthesia, and Immune Response
  • Cardiovascular Function and Risk Factors
  • Congenital heart defects research
  • Pharmacological Effects of Natural Compounds
  • Cholesterol and Lipid Metabolism
  • Electrochemical Analysis and Applications
  • Exercise and Physiological Responses

Capital Medical University
2022-2025

Vanderbilt University Medical Center
2019-2024

Nashville Oncology Associates
2024

Tianjin Medical University
2023

Discovery Institute
2016-2021

Sanford Burnham Prebys Medical Discovery Institute
2011-2021

Shihezi University
2021

Vanderbilt University
2019

Kunming University of Science and Technology
2017

Hunan University
2015

The ability of mammals to resist body fat accumulation is linked their expand the number and activity "brown adipocytes" within white depots. Activation β-adrenergic receptors (β-ARs) can induce a functional "brown-like" adipocyte phenotype. As cardiac natriuretic peptides (NPs) β-AR agonists are similarly potent at stimulating lipolysis in human adipocytes, we investigated whether NPs could mouse adipocytes acquire brown features, including capacity for thermogenic energy expenditure...

10.1172/jci59701 article EN Journal of Clinical Investigation 2012-02-06

Nuclear factor E2-related 2 (Nrf2) is a cap-n-collar basic leucine zipper (CNC-bZIP) transcription that well established as master regulator of phase II detoxification and antioxidant gene expression strongly expressed in tissues involved xenobiotic metabolism including liver kidney. Nrf2 also abundantly adipose tissue; however, the exact function adipocyte biology unclear. In current study we show targeted knock-out mice decreases tissue mass, promotes formation small adipocytes, protects...

10.1074/jbc.m109.093955 article EN cc-by Journal of Biological Chemistry 2010-01-21

A classic metabolic concept posits that insulin promotes energy storage and adipose expansion, while catecholamines stimulate release of stores by hydrolysis triglycerides through β-adrenergic receptor (βARs) protein kinase (PKA) signaling. Here, we have shown a key hub in the signaling pathway, activation p70 ribosomal S6 (S6K1) mTORC1, is also triggered PKA both mouse human adipocytes. Mice with mTORC1 impairment, either adipocyte-specific deletion Raptor or pharmacologic rapamycin...

10.1172/jci83532 article EN Journal of Clinical Investigation 2016-03-28

Prolonged exposure of rodent beta-cells to combinations cytokines induces the inducible form nitric oxide synthase (iNOS) expression and Fas expression, (NO) production, cell death. It also potential "defense" genes, such as manganese superoxide dismutase (MnSOD) heat shock protein (hsp) 70. NO is a radical with multifaceted actions. Recent studies have shown that NO, in addition having cytotoxic actions, may regulate gene transcription. remains unclear whether mediates cytokine-induced...

10.2337/diabetes.49.7.1116 article EN Diabetes 2000-07-01

Uncoupling protein (UCP) 2 is a widely expressed mitochondrial whose precise function still unclear but has been linked to mitochondria-derived reactive oxygen species production. Thus, the chronic absence of UCP2 potential promote persistent accumulation and an oxidative stress response. Here, we show that Ucp2−/− mice on three highly congenic (N >10) strain backgrounds (C57BL/6J, A/J, 129/SvImJ), including two independently generated sources Ucp2-null animals, all exhibit increased...

10.1210/en.2008-1642 article EN Endocrinology 2009-02-26

Nuclear factor E2–related 2 (Nrf2) is a transcription that functions as master regulator of the cellular adaptive response to oxidative stress. Our previous studies showed Nrf2 plays critical role in adipogenesis by regulating expression CCAAT/enhancer-binding protein β and peroxisome proliferator–activated receptor γ. To determine development obesity associated metabolic disorders, incidence syndrome was assessed whole-body or adipocyte-specific Nrf2-knockout mice on leptin-deficient ob/ob...

10.2337/db12-0584 article EN cc-by-nc-nd Diabetes 2012-12-14

Natriuretic peptide receptor C deficiency improves metabolism through signaling in adipose tissue, rather than skeletal muscle.

10.1126/scisignal.aam6870 article EN Science Signaling 2017-07-25

Little is known about the biological function of histone deacetylase 11 (HDAC11), which lone class IV HDAC. Here, we demonstrate that deletion HDAC11 in mice stimulates brown adipose tissue (BAT) formation and beiging white (WAT). Consequently, HDAC11-deficient exhibit enhanced thermogenic potential and, response to high-fat feeding, attenuated obesity, improved insulin sensitivity, reduced hepatic steatosis. Ex vivo cell-based assays revealed catalytic activity suppresses BAT...

10.1172/jci.insight.120159 article EN JCI Insight 2018-08-08

Objectives We investigated whether Angiotensin II (Ang II) modulates peripheral chemoreflex function through carotid body (CB) chemoreceptors in chronic heart failure (CHF).

10.1016/j.cardiores.2006.03.017 article EN Cardiovascular Research 2006-03-25

Objective Cardiac natriuretic peptides (NPs) bind to two receptors (NPRA‐mediator of signaling; NPRC‐clearance receptor) whose ratio, NPRR (NPRA/NPRC), determines the NP bioactivity. This study investigated relationship receptor gene expression in adipose tissue and muscle with obesity glucose intolerance. Prospectively, also assessed whether changes thermogenic markers accompanied improvements insulin sensitivity. Methods A cross‐sectional subjects a wide range BMI tolerance ( n = 50) was...

10.1002/oby.21418 article EN cc-by-nc Obesity 2016-02-17

Aims: The inability of pancreatic β-cells to secrete sufficient insulin in response glucose stimulation is a major contributing factor the development type 2 diabetes (T2D). We investigated both vitro and vivo effects deficiency nuclear factor-erythroid 2-related 1 (Nrf1) on β-cell function homeostasis. Results: Silencing Nrf1 leads pre-T2D phenotype with disrupted metabolism impaired secretion. Specifically, MIN6 stable knockdown (Nrf1-KD) isolated islets from β-cell-specific Nrf1-knockout...

10.1089/ars.2014.6017 article EN Antioxidants and Redox Signaling 2015-01-04

Activation of thermogenesis in brown adipose tissue (BAT) and the ability to increase uncoupling protein 1 (UCP1) levels mitochondrial biogenesis white fat (termed 'browning'), has great therapeutic potential treat obesity its comorbidities because net energy expenditure. β-adrenergic-cAMP-PKA signaling long been known regulate these processes. Recently PKA-dependent activation mammalian target rapamycin complex (mTORC1) was shown be necessary for 'browning' as well proper development...

10.1016/j.molmet.2017.12.017 article EN cc-by-nc-nd Molecular Metabolism 2018-01-17

Here, we show that β adrenergic signaling coordinately upregulates de novo lipogenesis (DNL) and thermogenesis in subcutaneous white adipose tissue (sWAT), both effects are blocked mice lacking the cAMP-generating G protein-coupled receptor Gs (Adipo-GsαKO) adipocytes. However, UCP1 expression but not DNL activation requires rapamycin-sensitive mTORC1. Furthermore, β3-adrenergic agonist CL316243 readily thermogenic lipogenic genes cultured adipocytes, indicating additional regulators must...

10.1016/j.celrep.2020.107598 article EN cc-by-nc-nd Cell Reports 2020-05-01

Decay-accelerating factor (DAF) is a cell-associated C regulatory protein that protects host cells from autologous attack. It functions intrinsically in cell surface membranes to rapidly dissociate classical and alternative pathway C3 convertases whenever these amplifying enzymes assemble on surfaces. composed of four contiguous approximately 70 amino acid long regions termed short consensus repeats (SCRs) share homology with similar units other convertase proteins. attached the membrane by...

10.4049/jimmunol.156.7.2528 article EN The Journal of Immunology 1996-04-01

Abstract Background The nucleotide oligomerization domain (NOD)-like receptor family pyrin containing 3 (NLRP3) in dorsal root ganglion (DRG) contributes to pain hypersensitivity multiple neuropathic models, but the function of NLRP3 diabetic (DNP) and regulation mechanism are still largely unknown. Epigenetic plays a vital role controlling gene expression. Ten-eleven translocation methylcytosine dioxygenase 2 (TET2) is DNA demethylase that transcriptional activation. TET2 also involved high...

10.1186/s12974-022-02669-7 article EN cc-by Journal of Neuroinflammation 2022-12-16

The estrogen-related receptor alpha gene encodes a nuclear protein, ERR alpha, whose structure is closely related to the estrogen receptors. modulates (ER)-mediated signaling pathways both positively and negatively. It selectively expressed in variety of cell types during development adult tissues. We have previously shown that stimulates expression mouse uterus. In this study, we found stimulated by uterus heart but not liver. Estrogen also human breast endometrial lines. promoter contains...

10.1210/en.2003-0432 article EN Endocrinology 2003-07-29

Receptor oligomerization is important for ligand binding and signal transduction. CD44 a transmembrane protein present on many cell types. One of the ligands hyaluronic acid (HA). HA activity linked to cellular activation in some Clustering has been speculated be HA. However, molecular mechanisms converting from an inactive receptor active are not known. Here we report that PMA stimulates by inducing clustering followed covalent homodimerization surface. Covalent dimerization involves...

10.4049/jimmunol.159.6.2702 article EN The Journal of Immunology 1997-09-15
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