PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy

被引:0
作者
Joseph Benetatos
Rachel E. Bennett
Harrison T. Evans
Sevannah A. Ellis
Bradley T. Hyman
Liviu-Gabriel Bodea
Jürgen Götz
机构
[1] The University of Queensland,Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute
[2] Harvard Medical School,Department of Neurology, MassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital
来源
Acta Neuropathologica | 2020年 / 140卷
关键词
Microglia; Neurodegeneration; Phagocytosis; PTEN; Synapse; Tau;
D O I
暂无
中图分类号
学科分类号
摘要
Phosphatase and tensin homolog (PTEN) regulates synaptic density in development; however, whether PTEN also regulates synapse loss in a neurodegenerative disorder such as frontotemporal lobar degeneration with Tau deposition (FTLD-Tau) has not been explored. Here, we found that pathological Tau promotes early activation of PTEN, which precedes apoptotic caspase-3 cleavage in the rTg4510 mouse model of FTLD-Tau. We further demonstrate increased synaptic and neuronal exposure of the apoptotic signal phosphatidylserine that tags neuronal structures for microglial uptake, thereby linking PTEN activation to synaptic and neuronal structure elimination. By applying pharmacological inhibition of PTEN's protein phosphatase activity, we observed that microglial uptake can be decreased in Tau transgenic mice. Finally, we reveal a dichotomous relationship between PTEN activation and age in FTLD-Tau patients and healthy controls. Together, our findings suggest that in tauopathy, PTEN has a role in the synaptotoxicity of pathological Tau and promotes microglial removal of affected neuronal structures.
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页码:7 / 24
页数:17
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