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成年齿状回中PTEN基因缺失会诱发癫痫。

PTEN DELETION IN THE ADULT DENTATE GYRUS INDUCES EPILEPSY.

作者信息

Yonan Jennifer M, Chen Kevin D, Baram Tallie Z, Steward Oswald

机构信息

Reeve-Irvine Research Center, Departments of Anatomy & Neurobiology, Neurobiology & Behavior, Neurosurgery, Pediatrics and Neurology, Center for the Neurobiology of Learning and Memory, University of California at Irvine, Irvine, CA 92697.

出版信息

bioRxiv. 2024 Aug 9:2024.08.07.606938. doi: 10.1101/2024.08.07.606938.

Abstract

Embryonic and early postnatal promotor-driven deletion of the phosphatase and tensin homolog (PTEN) gene results in neuronal hypertrophy, hyperexcitable circuitry and development of spontaneous seizures in adulthood. We previously documented that focal, vector-mediated PTEN deletion in mature granule cells of adult dentate gyrus triggers dramatic growth of cell bodies, dendrites, and axons, similar to that seen with early postnatal PTEN deletion. Here, we assess the functional consequences of focal, adult PTEN deletion, focusing on its pro-epileptogenic potential. PTEN deletion was accomplished by injecting AAV-Cre either bilaterally or unilaterally into the dentate gyrus of double transgenic PTEN-floxed, ROSA-reporter mice. Hippocampal recording electrodes were implanted for continuous digital EEG with concurrent video recordings in the home cage. Electrographic seizures and epileptiform spikes were assessed manually by two investigators, and corelated with concurrent videos. Spontaneous electrographic and behavioral seizures appeared after focal PTEN deletion in adult dentate granule cells, commencing around 2 months post-AAV-Cre injection. Seizures occurred in the majority of mice with unilateral or bilateral PTEN deletion and led to death in several cases. PTEN-deletion provoked epilepsy was not associated with apparent hippocampal neuron death; supra-granular mossy fiber sprouting was observed in a few mice. In summary, focal, unilateral deletion of PTEN in the adult dentate gyrus suffices to provoke time-dependent emergence of a hyperexcitable circuit generating hippocampus-origin, generalizing spontaneous seizures, providing a novel model for studies of adult-onset epileptogenesis.

摘要

胚胎期及出生后早期由启动子驱动的磷酸酶和张力蛋白同源物(PTEN)基因缺失会导致神经元肥大、神经回路兴奋性过高,并在成年后引发自发性癫痫。我们之前记录到,在成年齿状回的成熟颗粒细胞中通过载体介导进行局灶性PTEN缺失,会引发细胞体、树突和轴突的显著生长,这与出生后早期PTEN缺失的情况类似。在此,我们评估成年期局灶性PTEN缺失的功能后果,重点关注其致癫痫发作的潜在可能性。通过将腺相关病毒-重组酶(AAV-Cre)双侧或单侧注射到双转基因PTEN基因 floxed、ROSA报告基因小鼠的齿状回中,实现PTEN缺失。植入海马记录电极以进行连续数字脑电图记录,并在家笼中同时进行视频记录。由两名研究人员手动评估脑电图癫痫发作和癫痫样棘波,并与同步视频相关联。在成年齿状颗粒细胞中局灶性PTEN缺失后出现了自发性脑电图和行为性癫痫发作,大约在注射AAV-Cre后2个月开始。大多数单侧或双侧PTEN缺失的小鼠出现了癫痫发作,并有几例导致死亡。PTEN缺失引发的癫痫与明显的海马神经元死亡无关;在少数小鼠中观察到了颗粒上层苔藓纤维发芽。总之,成年齿状回中局灶性、单侧PTEN缺失足以引发超兴奋性回路随时间出现,产生海马起源的全身性自发性癫痫发作,为成年期癫痫发生的研究提供了一个新模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d64/11326251/6a3fd7097a37/nihpp-2024.08.07.606938v1-f0001.jpg

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