Rappaport Research Institute and Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Institute of Molecular Biology and Biotechnology (IMBB), Foundation for Research and Technology - Hellas (FORTH), Heraklion, Greece.
Elife. 2019 Jul 16;8:e44745. doi: 10.7554/eLife.44745.
The inability of differentiated cells to maintain their identity is a hallmark of age-related diseases. We found that the transcription factor Hey supervises the identity of differentiated enterocytes (ECs) in the adult midgut. Lineage tracing established that Hey-deficient ECs are unable to maintain their unique nuclear organization and identity. To supervise cell identity, Hey determines the expression of nuclear lamins, switching from a stem-cell lamin configuration to a differentiated lamin configuration. Moreover, continued Hey expression is required to conserve large-scale nuclear organization. During aging, Hey levels decline, and EC identity and gut homeostasis are impaired, including pathological reprograming and compromised gut integrity. These phenotypes are highly similar to those observed upon acute targeting of Hey or perturbation of lamin expression in ECs in young adults. Indeed, aging phenotypes were suppressed by continued expression of Hey in ECs, suggesting that a Hey-lamin network safeguards nuclear organization and differentiated cell identity.
分化细胞丧失其特性是与年龄相关疾病的一个标志。我们发现转录因子 Hey 调控成年中肠分化肠细胞(EC)的特性。谱系追踪确立了 Hey 缺陷型 EC 无法维持其独特的核组织和特性。为了调控细胞特性,Hey 决定核纤层蛋白的表达,从干细胞纤层蛋白结构转换为分化的纤层蛋白结构。此外,持续的 Hey 表达需要保存大规模的核组织。在衰老过程中,Hey 水平下降,EC 特性和肠道内稳态受损,包括病理性重编程和肠道完整性受损。这些表型与在年轻人中急性靶向 Hey 或干扰 EC 中纤层蛋白表达所观察到的表型非常相似。事实上,通过在 EC 中持续表达 Hey 可以抑制衰老表型,这表明 Hey-纤层蛋白网络可保护核组织和分化细胞特性。