中文

Faculty

Wusheng Xiao

Wusheng Xiao

Wusheng Xiao

  • Assistant Professor
  • wxiao@bjmu.edu.cn
Personal profile

Dr. Xiao is a tenure-track Assistant Professor at Department of Toxicology, School of Public Health of Peking University. Before joining PKU in November 2022, He was a postdoctoral fellow, instructor, associate scientist, and faculty member under the mentorship of Dr. Joseph Loscalzo at Brigham and Women’s Hospital and Harvard Medical School from 2015 to 2022. Dr. Xiao obtained his Ph.D. degree in Free Radical and Radiation Biology from the University of Iowa in 2014 after completion of his Master degree in Environmental and Occupational Medicine at Fudan University in 2010 and his Bachelor degree in Preventive Medicine at Nanchang University in 2006. He has published 17 first-authorship and co-authorship publications and participated in 3 NIH and NIEHS funded research projects.

Main research directions

Cardiovascular and pulmonary diseases (CVPDs) are the top leading causes of death in China and worldwide. The morbidity and mortality of such diseases has been linked to environmental pollution. The central focuses of our research are to decipher the mechanisms by which environmental pollutants damage the cardiovascular and pulmonary systems and exacerbate the risk of CVPDs with the goal of developing new preventive and therapeutic approaches for CVPDs.

Project 1: Energy metabolism and cardiopulmonary vasculature injury.

Energy metabolism is a fundamental survival mechanism for all mammals. Metabolic alterations have been implicated in the development of many CVPDs. We aim to investigate the crucial roles of metabolic pathways and metabolites in regulating environmental biohazards e.g., heavy metals, pesticides, and nanomaterials induced damages in the cardiovascular and pulmonary systems.

Project 2: Redox stresses and cardiopulmonary vasculature dysfunctions.

Cellular redox homeostasis is finely tuned by antioxidants (antioxidant enzymes and nonenzymatic antioxidants) and pro-oxidants (reactive oxygen/nitrogen species; ROS/RNS). Imbalance between these two arms leads to redox stresses including oxidative stress and reductive stress, both of which are detrimental to biological processes. We aim to elucidate how environmental pollutants perturb cellular redox balance leading to cardiopulmonary vasculature dysfunctions.

Representative scientific research projects

1. US NIH R01 Project: L-2-hydroxyglutarate and metabolic remodeling in hypoxia. Researcher; 2020-2022

2. US NIH NIH R37 Project:GPx-3 and peroxide flux in the endothelial cell. Researcher; 2015-2017

3. US NIEHS Iowa Superfund Project:Semi-volatile PCB exposure and oxidative stress in mammalian cells. Researcher; 2010-2014

10 representative papers

1. He H, Mulhern RM, Oldham WM, Xiao W, Lin Y, Liao R, Loscalzo J. L-2-hydroxyglutarate protects against cardiac injury via metabolic remodeling. Circulation Research. 2022, 131: 562-579.

2. Xiao W, Oldham WM, Priolo C, Pandey AK, Loscalzo J. Immunometabolic endothelial phenotypes: integrating inflammation and glucose metabolism. Circulation Research. 2021, 129: 9-29.

3. Xiao W and Loscalzo J. Metabolic response to reductive stress. Antioxidants & Redox Signaling. 2020, 32: 1330-1347.

4. Xiao W, Wang RS, Handy DE, Loscalzo J. NAD(H) and NADP(H) redox couples and cellular energy metabolism. Antioxidants & Redox Signaling. 2018, 28: 251-272.

5. Xiao W, Sarsour EH, Wagner BA, Doskey CM., Buettner GR, Domann FE, Goswami PC. Succinate dehydrogenase activity regulates PCB3-quinone induced metabolic oxidative stress and toxicity in HaCaT human keratinocytes. Archives of Toxicology. 2016, 90: 319-332.

6. Xiao W, Vorrink SU, Domann FE, Goswami PC. Ligand-independent activation of aryl hydrocarbon receptor signaling in PCB3-quinone treated HaCaT human keratinocytes. Toxicology Letters. 2015, 233: 258-266.

7. Xiao W and Goswami PC. Down-regulation of peroxisome proliferator activated receptor γ coactivator 1α induces oxidative stress and toxicity of 1-(4-Chlorophenyl)-benzo-2,5-quinone in HaCaT human keratinocytes. Toxicology In Vitro. 2015, 29: 1332-1338.

8. Xiao W, Zhu Y, Sarsour EH, Kalen AL, Aykin-Burns N, Spitz DR, Goswami PC. Selenoprotein P regulates 1-(4-Chlorophenyl)-benzo-2,5-quinone induced oxidative stress and toxicity in human keratinocytes. Free Radical Biology and Medicine. 2013, 65: 70-77.

9. Xiao W, Zhang J, Liang J, Zhu H, Zhou Z, Wu Q. Adverse effects of neonatal exposure 3,3',4,4',5,5'-hexachlorobiphenyl on hormone levels and testicular function in male Sprague-Dawley rats. Environmental Toxicology. 2011, 26: 657-668.

10. Xiao W, Li K, Wu Q, Nishimura N, Chang X, Zhou Z. Influence of persistent thyroxine reduction on spermatogenesis in rats neonatally exposed to 2,2',4,4',5,5'-hexachlorobiphenyl. Birth Defects Research. 2010, 89: 18-25.