Kwon Ji Hyun, Kim Hyun Kyu, Ha Tae Won, Im Jeong Suk, Song Byung Hoo, Hong Ki Sung, Oh Jae Sang, Han Jaeseok, Lee Man Ryul
Soonchunhyang Institute of Medi-bio Science (SIMS), Soon Chun Hyang University, Cheonan 31151, Korea.
Department of Medicine, Konkuk University School of Medicine and Mirae Cell Bio Co. LTD., Seoul 05029, Korea.
Biomedicines. 2020 Jun 26;8(6):176. doi: 10.3390/biomedicines8060176.
Various types of stress stimuli have been shown to threaten the normal development of embryos during embryogenesis. Prolonged heat exposure is the most common stressor that poses a threat to embryo development. Despite the extensive investigation of heat stress control mechanisms in the cytosol, the endoplasmic reticulum (ER) heat stress response remains unclear. In this study, we used human embryonic stem cells (hESCs) to examine the effect of heat stress on early embryonic development, specifically alterations in the ER stress response. In a hyperthermic (42 °C) culture, ER stress response genes involved in hESC differentiation were induced within 1 h of exposure, which resulted in disturbed and delayed differentiation. In addition, hyperthermia increased the expression levels of activating transcription factor 4 (ATF4) and C/EBP homologous protein (CHOP) genes, which are associated with the protein kinase RNA-like endoplasmic reticulum kinase (PERK) signaling pathway. Furthermore, we demonstrated that tauroursodeoxycholic acid, a chemical chaperone, mitigated the delayed differentiation under hyperthermia. Our study identified novel gene markers in response to hyperthermia-induced ER stress on hESCs, thereby providing further insight into the mechanisms that regulate human embryogenesis.
各种类型的应激刺激已被证明会在胚胎发生过程中威胁胚胎的正常发育。长时间受热是对胚胎发育构成威胁的最常见应激源。尽管对胞质溶胶中的热应激控制机制进行了广泛研究,但内质网(ER)热应激反应仍不清楚。在本研究中,我们使用人类胚胎干细胞(hESC)来研究热应激对早期胚胎发育的影响,特别是内质网应激反应的改变。在高温(42°C)培养中,参与hESC分化的内质网应激反应基因在暴露后1小时内被诱导,这导致分化受到干扰和延迟。此外,高温增加了与蛋白激酶RNA样内质网激酶(PERK)信号通路相关的激活转录因子4(ATF4)和C/EBP同源蛋白(CHOP)基因的表达水平。此外,我们证明化学伴侣牛磺熊去氧胆酸减轻了高温下的延迟分化。我们的研究确定了hESC对高温诱导的内质网应激反应的新基因标记,从而为调节人类胚胎发生的机制提供了进一步的见解。