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PTEN 激活有助于小胶质细胞在 tau 病中吞噬神经元和突触。

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

机构信息

Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.

Department of Neurology, MassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA.

出版信息

Acta Neuropathol. 2020 Jul;140(1):7-24. doi: 10.1007/s00401-020-02151-9. Epub 2020 Mar 31.

Abstract

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.

摘要

磷酸酶和张力蛋白同源物(PTEN)调节发育过程中的突触密度;然而,PTEN 是否也调节神经退行性疾病(如伴有 Tau 沉积的额颞叶变性(FTLD-Tau))中的突触丢失尚未被探索。在这里,我们发现病理性 Tau 促进了 PTEN 的早期激活,这先于 rTg4510 FTLD-Tau 小鼠模型中凋亡 Caspase-3 的裂解。我们进一步证明了凋亡信号磷脂酰丝氨酸的突触和神经元暴露增加,该信号标记神经元结构以供小胶质细胞摄取,从而将 PTEN 激活与突触和神经元结构消除联系起来。通过应用药理学抑制 PTEN 的蛋白磷酸酶活性,我们观察到 Tau 转基因小鼠中的小胶质细胞摄取可以减少。最后,我们揭示了 FTLD-Tau 患者和健康对照者中 PTEN 激活与年龄之间的二分关系。总之,我们的研究结果表明,在 Tau 病中,PTEN 在病理性 Tau 的突触毒性中起作用,并促进受影响的神经元结构的小胶质细胞清除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0261/7300099/5b99200028f8/401_2020_2151_Fig1_HTML.jpg

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