Chen, Xiaoying

Date:2018-11-08
Associate professor, Tsinghua University
PI, IDG/McGovern Institute, Tsinghua University;Tsinghua-Peking Center for Life Sciences;Institute for Immunology
 
Mailing address:
Tsinghua University, Medical Science Building Room C115, 30. Shuang qing Road, Beijing, China, 100085 

Email:xiaoyingchen@tsinghua.edu.cn

[Research Focus]

Alzheimer’s disease is the most common neurodegenerative disorder. Pathologically, it is characterized by the aggregation of misfolded proteins, including extracellular deposition of amyloid-β (Aβ) as plaques and intracellular accumulation of aggregated tau as neurofibrillary tangles. The regional progression of brain atrophy in Alzheimer’s disease highly correlates with tau accumulation but not amyloid deposition, and the mechanisms of tau-mediated neurodegeneration remain elusive.
Innate immune responses represent a common pathway for the initiation and progression of some neurodegenerative diseases. So far, little is known about the extent or role of the adaptive immune response and its interaction with the innate immune response in the presence of amyloid-β or tau pathology. Our research first demonstrated that the adaptive immune response drives tau-mediated neurodegeneration and cognitive decline. These findings answer a fundamental question of how does tau aggregation lead to regional neuronal death. A deeper understanding of both innate and adaptive immune responses across the progression of AD is likely to reveal novel therapeutic strategies for both preclinical and clinically symptomatic stages of the disease.
My lab focuses on understanding the brain-body interactions in health and disease. Interdisciplinary approaches including, single-cell multi-omics, metabolisms, clarity imaging, in vivo calcium imaging, optogenetics, and in vivo CRISPR gene editing, are applied in understanding the dialogue of brain-immune communication and developing potential therapeutic tools. The major research directions in my lab are
1.Decoding the immune responses in Alzheimer’s disease and therapeutics development
2.Deciphering the brain-immune interface and brain-body interaction
3.Understanding neuronal plasticity throughout Alzheimer’s disease progression

[Education & Experience]

2025-               Associate Professor and Principal Investigator                        

                        IDG/McGovern Institute for Brain Research at Tsinghua University                        
                        Institute for Immunology at Tsinghua University                        
                        Tsinghua-Peking Center for Life Sciences                        
                        Brain-immune communication in Alzheimer’s disease
2023-2024       Instructor in the lab of Dr. David Holtzman
                        Department of Neurology, Washington University, School of Medicine
                        Neuroimmunology and approaches for the treatment of Alzheimer’s disease
2019-2022       Postdoctoral fellow in the lab of Dr. David Holtzman
                        Department of Neurology, Washington University, School of Medicine
                        APOE and immune response in Alzheimer’s disease  
2017-2019       Postdoctoral fellow in the lab of Dr. Azad Bonni
                        Department of Neuroscience, Washington University, School of Medicine
                        Genetic and epigenetic regulations in learning in adult mammalian brain
2009-2016       PhD dissertation
                        Departments of Immunology, Neuroscience, Tongji University        
                        David Geffen School of Medicine, UCLA
                        Neuronal development and maturation
 

[Selected awards]

2024   Jeffrey L. Morby Prize for Best Research in Alzheimer’s Disease, Cure Alzheimer’s Fund 
2023   Early Career Achievement Award, Alzheimer's Association 
2023   AAIC Advancements: Immunity Travel Award, Alzheimer's Association
2023   AAIC Advancements: APOE Travel Award, Alzheimer's Association
2022   Trainee Professional Development Award, Society of Neuroscience
2022   Brain Immunology and Glia Travel Award, Washington University School of Medicine 
2022   Poletsky Award, Alzheimer’s Disease Research Center 
2022   O’Leary Prize for Best Research in Neuroscience, Washington University

[Selected Publications]

I-Brain-immune communication in Alzheimer’s disease

Carling G, Fan L, Foxe N, Norman K, Wong M, Zhu D, Corona C, Razzoli A, Yu F, Yarahmady A, Ye P, Chen H, Huang Y, Amin S, Sereda R, Lopez-lee C, Zacharioudakis E, Chen X, Xu J, Cheng F, Gavathiotis E, Cuervo A, Holtzman D, Mok S, Sinha S, Sidoli S, Ratan R, Luo W, Gong S, Gan L. Alzheimer’s disease-linked risk alleles elevate microglial cGAS-associated senescence and neurodegeneration in a tauopathy model. 2024. Neuron. 112. 1-20, PMID: 38328219  

AAIC, Kloske C, Tansey M, Wilcock D (Chen X, leading the study of Microglia-mediated T-cell infiltration and reactivity) Advancements in Immunity and Dementia Research: Highlights from the 2023 AAIC Advancements: Immunity Conference. 2024. Alzheimer’s and Dementia. PMID: 39692624

AAIC, Kloske C, Bu G, Goate A, Holtzman D (Chen X, leading the study of APOE and immune response in Alzheimer’s Disease) Advancements in APOE and dementia research: Highlights from the 2023 AAIC Advancements: APOE conference. 2024. Alzheimer’s and Dementia. 20, 5815-6664, PMID: 39031528

Chen X, Firulyova M, Manis M, Herz J, Smirnov I, Aladyeva E, Wang C, Bao X, Finn M, Hu H, Shchukina I, Kim M, Yuede C, Kipnis J, Artyomov M, Ulrich J, Holtzman D. Microglia-mediated T cell infiltration drives neurodegeneration in tauopathy. 2023. Nature. 615, 668-677, PMID: 36890231

Chen X, Holtzman D. Emerging roles of innate and adaptive immunity in Alzheimer’s Disease. 2022. Immunity. 55, 2236-2254, PMID: 36351425

II-Genetic and epigenetic regulations in learning in adult mammalian brain

Cellular diversification is critical for specialized functions of the brain including learning and memory. Single-cell RNA sequencing facilitates transcriptomic profiling of distinct major types of neurons, but the divergence of transcriptomic profiles within a specific neuronal population and their link to function remain poorly understood. Using single cell multi-omics, in vivo calcium imaging, optogenetics, CRISPR knockout, and behavior analyses, I discovered a subpopulation neuron that specifically undergoes transcriptomic plasticity in response to neuronal activity and learning. Those findings answer the fundamental question of how diversification of neurons influences learning and memory and opens an entirely new and exciting direction of research in neuroscience for studying functional diversity in subtypes of neurons in response to environmental changes.  

Chen X, Du Y, Broussard J, Kislin M, Yuede C, Zhang S, Dietmann S, Gabel H, Zhao G, Wang S, Zhang X, Bonni A. Transcriptomic mapping uncovers Purkinje neuron plasticity driving learning. 2022. Nature. 605, 722-727, PMID: 35545673 

Chen X, Zhang B, Wang T, Bonni A, Zhao G. Robust principal component analysis for accurate outlier detection in RNA-Seq data. 2020. BMC Bioinformatics. 21, 269. PMID: 32600248

Chen X, Chanda A, Ikeuchi Y, Zhang X, Goodman JV, Reddy NC, Majidi SP, Wu DY, Smith SE, Godec A, Oldenborg A, Gabel HW, Zhao G, Bonni S, Bonni A. Transcriptional regulator SnoN promotes proliferation of cerebellar granule neuron precursors in the postnatal mouse brain. 2019. J Neurosci. 39, 44-62. PMID: 30425119  

Smith SE, Chen X, Brier L, Bumstead J, Rensing N, Epstein A, Oldenborg A, Crowley J, Bice A, Dikranian K, Ippolito J, Haigis M, Papouin T, Zhao G, Wong M, Culver JP, Bonni A. Astrocyte deletion of α2-Na/K ATPase triggers episodic motor paralysis in mice via a metabolic pathway. 2020. Nature Communication. 11, 6164. PMID: 33268780

Krishnan N, Chen X, Donnelly-Roberts D, Mohler E.G, Holtzman D. M, Gopalakrishnan, S. M. Small molecule phenotypic screen identifies novel regulators of LDLR expression. 2020. ACS Chem Biol.15, 3262-3274. PMID: 33270420

III-Immune signaling in neuronal maturation

I studied the molecular and cellular mechanisms governing neuropsychiatric disorders by using functional subtype-specific neurons derived from human embryonic stem cells (hESCs) and induced pluripotent stem cells (hiPSCs). I discovered that MeCP2-deficient human ESCs/iPSCs-derived neurons showed aberrant immature action potentials and synaptic transmission. To capture the molecular mechanisms governing neuron electrophysiological maturation at single cell level, I therefore developed electrophysiological recording coupled with single cell transcriptome analysis (Patch-Seq) and revealed a tight link between neuronal maturation and genes involved in ubiquitination, immune function, and oxidative phosphorylation.

Chen X*, Han X, Blanchi B, Guan W, Ge W, Yu YC*, Sun YE*. Graded and pan-neural disease phenotypes of Rett Syndrome linked with dosage of functional MeCP2. 2020. Protein Cell. 12, 639-652. PMID: 32851591 (co-corresponding author)

Chen X, Zhang K, Zhou L, Gao X, Wang J, Yao Y, He F, Luo Y, Yu Y, Li S, Cheng L, Sun YE.Coupled electrophysiological recording and single cell transcriptome analyses revealed molecular mechanisms underlying neuronal maturation. 2016. Protein Cell. 7, 175-186. PMID: 26883038 (Cover research)

Chen Y, Yu J, Niu Y, Qin D, Liu H, Li G, Hu Y, Wang J, Lu Y, Kang Y, Jiang Y, Wu K, Li S, Wei J, He J, Wang J, Liu X, Luo Y, Si C, Bai R, Zhang K, Liu J, Huang S, Chen Z, Wang S, Chen X, Bao X, Zhang Q, Li F, Geng R, Liang A, Shen D, Jiang T, Hu X, Ma Y, Ji W, Sun YE. Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys.2017. Cell. 169, 945-955. PMID: 28525759

Liu H, Chen Y, Niu Y, Zhang K, Kang Y, Ge W, Liu X, Zhao E, Wang C, Lin S, Jing B, Si C, Lin Q, Chen X, Lin H, Pu X, Wang Y, Qin B, Wang F, Wang H, Si W, Zhou J, Tan T, Li T, Ji S, Xue Z, Luo Y, Cheng L, Zhou Q, Li S, Sun YE, Ji W. TALEN-mediated gene mutagenesis in rhesus and cynomolgus monkeys. 2014. Cell Stem Cell. 14, 323-328. PMID: 24529597