Hyun Sung-Ae, Lee Young Ju, Jang Sumi, Ko Moon Yi, Lee Chang Youn, Cho Yong Woo, Yun Ye Eun, Lee Byoung-Seok, Seo Joung-Wook, Moon Kyoung-Sik, Ka Minhan
Department of Advanced Toxicology Research, Korea Institute of Toxicology, KRICT, Daejeon, 34114, Republic of Korea.
Department of Materials Science and Chemical Engineering, Hanyang University, Ansan, 15588, Republic of Korea.
Stem Cell Res Ther. 2022 Mar 21;13(1):110. doi: 10.1186/s13287-022-02785-4.
Corticosterone (CORT) can induce neuronal damage in various brain regions, including the cerebral cortex, the region implicated in depression. However, the underlying mechanisms of these CORT-induced effects remain poorly understood. Recently, many studies have suggested that adipose stem cell-derived extracellular vesicles (A-EVs) protect neurons in the brain.
To investigated neuroprotection effects of A-EVs in the CORT-induced cortical neurons, we cultured cortical neurons from E15 mice for 7 days, and the cultured cortical neurons were pretreated with different numbers (5 × 10-10 per mL) of A-EVs (A-EVs, A-EVs, A-EVs) for 30 min followed by administration of 200 μM CORT for 24 h.
Here, we show that A-EVs exert antiapoptotic effects by inhibiting endoplasmic reticulum (ER) stress in CORT-induced cortical neurons. We found that A-EVs prevented neuronal cell death induced by CORT in cultured cortical neurons. More importantly, we found that CORT exposure in cortical neurons resulted in increased levels of apoptosis-related proteins such as cleaved caspase-3. However, pretreatment with A-EVs rescued the levels of caspase-3. Intriguingly, CORT-induced apoptosis involved upstream activation of ER stress proteins such as GRP78, CHOP and ATF4. However, pretreatment with A-EVs inhibited ER stress-related protein expression.
Our findings reveal that A-EVs exert antiapoptotic effects via inhibition of ER stress in CORT-induced cell death.
皮质酮(CORT)可在包括大脑皮层(与抑郁症相关的区域)在内的各个脑区诱导神经元损伤。然而,这些CORT诱导效应的潜在机制仍知之甚少。最近,许多研究表明脂肪干细胞衍生的细胞外囊泡(A-EVs)可保护大脑中的神经元。
为了研究A-EVs对CORT诱导的皮质神经元的神经保护作用,我们从E15小鼠中培养皮质神经元7天,并将培养的皮质神经元用不同数量(每毫升5×10-10)的A-EVs预处理30分钟,然后给予200μM CORT处理24小时。
在此,我们表明A-EVs通过抑制CORT诱导的皮质神经元中的内质网(ER)应激发挥抗凋亡作用。我们发现A-EVs可防止培养的皮质神经元中CORT诱导的神经元细胞死亡。更重要的是,我们发现皮质神经元中暴露于CORT会导致凋亡相关蛋白(如裂解的caspase-3)水平升高。然而,用A-EVs预处理可挽救caspase-3的水平。有趣的是,CORT诱导的凋亡涉及ER应激蛋白(如GRP78、CHOP和ATF4)的上游激活。然而,用A-EVs预处理可抑制ER应激相关蛋白的表达。
我们的研究结果表明,A-EVs通过抑制CORT诱导的细胞死亡中的ER应激发挥抗凋亡作用。