GJA1-20K Enhances Mitochondria Transfer from Astrocytes to Neurons via Cx43-TnTs After Traumatic Brain Injury

被引:33
作者
Ren, Dabin [1 ]
Zheng, Ping [1 ]
Zou, Shufeng [2 ]
Gong, Yuqin [3 ]
Wang, Yang [2 ]
Duan, Jian [2 ]
Deng, Jun [4 ]
Chen, Haiming [4 ]
Feng, Jiugeng [2 ]
Zhong, Chunlong [5 ]
Chen, Wei [1 ,5 ]
机构
[1] Shanghai Univ Med & Hlth Sci, Peoples Hosp Shanghai Pudong New Area, Dept Neurosurg, Shanghai 201299, Peoples R China
[2] Nanchang Univ, Affiliated Hosp 1, Dept Neurosurg, Nanchang 330008, Jiangxi, Peoples R China
[3] Nanchang Univ, Affiliated Hosp 2, Dept Operat Room, Nanchang NANCHANG UN, Jiangxi, Peoples R China
[4] Nanchang Univ, Affiliated Hosp 1, Trauma Ctr, Dept Emergency, Nanchang 330008, Jiangxi, Peoples R China
[5] Tongji Univ, Shanghai East Hosp, Dept Neurosurg, Shanghai 201200, Peoples R China
基金
中国国家自然科学基金;
关键词
Traumatic brain injury; Astrocyte; Mitochondria transfer; GJA1-20K; Cx43; HEMICHANNELS; CHANNELS; PHOSPHORYLATION; INHIBITION; CONNEXIN43; MODEL; CX43; RAT;
D O I
10.1007/s10571-021-01070-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Astrocytes are crucial in neural protection after traumatic brain injury (TBI), a global health problem causing severe brain tissue damage. Astrocytic connexin 43 (Cx43), encoded by GJA1 gene, has been demonstrated to facilitate the protection of astrocytes to neural damage with unclear mechanisms. This study aims to explore the role of GJA1-20K/Cx43 axis in the astrocyte-neuron interaction after TBI and the underlying mechanisms. Primarily cultured cortical neurons isolated from embryonic C57BL/6 mice were treated by compressed nitrogen-oxygen mixed gas to simulate TBI-like damage in vitro. The transwell astrocyte-neuron co-culture system were constructed to recapitulate the interaction between the two cell types. Quantitative PCR was applied to analyze mRNA level of target genes. Western blot and immunofluorescence were conducted to detect target proteins expression. GJA1-20K overexpression significantly down-regulated the expression of phosphorylated Cx43 (p-Cx43) without affecting the total Cx43 protein level. Besides, GJA1-20K overexpression obviously enhanced the dendrite length, as well as the expression levels of function and synthesis-related factors of mitochondria in damaged neurons. GJA1-20K up-regulated functional Cx43 expression in astrocytes, which promoted mitochondria transmission from astrocytes to neurons which might be responsible to the protection of astrocyte to neurons after TBI-like damage in vitro.
引用
收藏
页码:1887 / 1895
页数:9
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