Division of Intractable Disease Research, Korea National Institute of Health, Osong, Cheongju, 28160, Republic of Korea.
Center for National Stem Cell and Regenerative Medicine 202, Osongsaengmyung 2-Ro, Heundeok-Gu, Cheongju, Chungcheongbuk-Do, 28160, Republic of Korea.
Sci Rep. 2023 Apr 7;13(1):5683. doi: 10.1038/s41598-023-32567-8.
Cultured human pluripotent stem cells (hPSCs) grow as colonies that require breakdown into small clumps for further propagation. Although cell death mechanism by single-cell dissociation of hPSCs has been well defined, how hPSCs respond to the deadly stimulus and recover the original status remains unclear. Here we show that dissociation of hPSCs immediately activates ERK, which subsequently activates RSK and induces DUSP6, an ERK-specific phosphatase. Although the activation is transient, DUSP6 expression persists days after passaging. DUSP6 depletion using the CRISPR/Cas9 system reveals that DUSP6 suppresses the ERK activity over the long term. Elevated ERK activity by DUSP6 depletion increases both viability of hPSCs after single-cell dissociation and differentiation propensity towards mesoderm and endoderm lineages. These findings provide new insights into how hPSCs respond to dissociation in order to maintain pluripotency.
培养的人类多能干细胞(hPSCs)以集落的形式生长,需要将其分解成小团块以进一步繁殖。尽管 hPSC 单细胞分离的细胞死亡机制已经得到很好的定义,但 hPSC 如何应对致命刺激并恢复原始状态尚不清楚。在这里,我们表明 hPSC 的分离立即激活 ERK,随后激活 RSK 并诱导 DUSP6,一种 ERK 特异性磷酸酶。尽管激活是短暂的,但 DUSP6 的表达在传代数天后仍持续存在。使用 CRISPR/Cas9 系统耗尽 DUSP6 表明 DUSP6 长期抑制 ERK 活性。通过 DUSP6 耗竭增加 ERK 活性可提高单细胞分离后 hPSC 的存活率,并增加向中胚层和内胚层谱系分化的倾向。这些发现为 hPSC 如何应对分离以维持多能性提供了新的见解。