HONGJUN (Harry) FU

Dr. HONGJUN (Harry) FU

Department of Neuroscience, The Ohio State University Wexner Medical Center, Columbus, OH 43210 USA
orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2016 in Nature Neuroscience
Verified
Journal Article
Open access
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JWJessica W Wu
Jessica W Wu
SHS Abid Hussaini
S Abid Hussaini
IBIsle M Bastille
Isle M Bastille
GRGustavo A Rodriguez
Gustavo A Rodriguez
AMAna Mrejeru
Ana Mrejeru
KDKaren E Duff
Karen E Duff
The authors show that tau can be released by neurons and transferred to other neurons via the extracellular space. Moreover, they show that enhancing neuronal activity accelerates transneuronal tau propagation and exacerbates tau pathology. Tau protein can transfer between neurons transneuronally and trans-synaptically, which is thought to explain the progressive spread of tauopathy observed in the brain of patients with Alzheimer's disease. Here we show that physiological tau released from donor cells can transfer to recipient cells via the medium, suggesting that at least one mechanism by which tau can transfer is via the extracellular space. Neuronal activity has been shown to regulate tau secretion, but its effect on tau pathology is unknown. Using optogenetic and chemogenetic approaches, we found that increased neuronal activity stimulates the release of tau in vitro and enhances tau pathology in vivo. These data have implications for disease pathogenesis and therapeutic strategies for Alzheimer's disease and other tauopathies.

24 September 2018 in Nature Neuroscience
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Journal Article
Closed access
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HFHONGJUN (Harry) FU
HONGJUN (Harry) FU
JHJohn Hardy
John Hardy
KDKaren E. Duff
Karen E. Duff

25 March 2021 in Nature Communications
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Journal Article
Open access
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JWJuexin Wang
Juexin Wang
AMANJUN MA
ANJUN MA
YCYuzhou Chang
Yuzhou Chang
JGJianting Gong
Jianting Gong
YJYuexu Jiang
Yuexu Jiang
DXDong Xu
Dong Xu
Single-cell RNA-sequencing (scRNA-Seq) is widely used to reveal the heterogeneity and dynamics of tissues, organisms, and complex diseases, but its analyses still suffer from multiple grand challenges, including the sequencing sparsity and complex differential patterns in gene expression. We introduce the scGNN (single-cell graph neural network) to provide a hypothesis-free deep learning framework for scRNA-Seq analyses. This framework formulates and aggregates cell–cell relationships with graph neural networks and models heterogeneous gene expression patterns using a left-truncated mixture Gaussian model. scGNN integrates three iterative multi-modal autoencoders and outperforms existing tools for gene imputation and cell clustering on four benchmark scRNA-Seq datasets. In an Alzheimer’s disease study with 13,214 single nuclei from postmortem brain tissues, scGNN successfully illustrated disease-related neural development and the differential mechanism. scGNN provides an effective representation of gene expression and cell–cell relationships. It is also a powerful framework that can be applied to general scRNA-Seq analyses.

1 February 2017 in Neuron
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Journal Article
Closed access
HFHONGJUN (Harry) FU
HONGJUN (Harry) FU
GRGustavo A. Rodriguez
Gustavo A. Rodriguez
MHMathieu Herman
Mathieu Herman
SESheina Emrani
Sheina Emrani
ENEden Nahmani
Eden Nahmani
KDKaren E. Duff
Karen E. Duff

17 December 2018 in Nature Neuroscience
Verified
Journal Article
Closed access
HFHONGJUN (Harry) FU
HONGJUN (Harry) FU
APAndrea Possenti
Andrea Possenti
RFRosie Freer
Rosie Freer
YNYoshikazu Nakano
Yoshikazu Nakano
NVNancy C. Hernandez Villegas
Nancy C. Hernandez Villegas
KDKaren E. Duff
Karen E. Duff

27 June 2022 in Nature Neuroscience
Verified
Journal Article
Closed access
PDF file
MKMor Kenigsbuch
Mor Kenigsbuch
PBPierre Bost
Pierre Bost
SHShahar Halevi
Shahar Halevi
YCYuzhou Chang
Yuzhou Chang
SCShuo Chen
Shuo Chen
IAIdo Amit
Ido Amit