Department of Clinical Medicine and Surgery, University of Naples "Federico II", Via S. Pansini 5, 80131, Naples, Italy.
J Endocrinol Invest. 2018 Jan;41(1):59-66. doi: 10.1007/s40618-017-0737-4. Epub 2017 Aug 29.
Thyroid hormone is a major determinant of tissue functions in vivo. The deiodinase family controls the tissue-specific activation or inactivation of intracellular thyroid hormones. Precise control of the T3-dependent transcriptional program is required by multiple cell systems, including the stem cell. In this context, the identification of a close connection between thyroid hormones and different signal pathways involved in the control of stem cell functions suggested that the deiodinases may play a role in the definition of stem cell biology and physiology. Stem cells have an unlimited self-renewal capacity and the potential to differentiate into different types of mature cells. Deciphering how all these events are achieved, how the T3 signal is controlled and integrated in stem cells and their niches, and how it can impact on them is essentially unknown and represents a challenge for coming years. In this review, I will explore the role played by the deiodinases in the modulation of the TH signal in stem cells of adult tissues, namely muscle and intestine, and how their actions control the delicate balance among self-renewal, proliferation and differentiation. Elucidation of the molecular mechanisms presiding thyroid hormone action in stem cells may reveal therapeutic potential, for example in the fields of regenerative diseases and cancer.
甲状腺激素是体内组织功能的主要决定因素。脱碘酶家族控制细胞内甲状腺激素的组织特异性激活或失活。包括干细胞在内的多个细胞系统都需要对 T3 依赖性转录程序进行精确控制。在这种情况下,甲状腺激素与参与控制干细胞功能的不同信号通路之间的紧密联系表明,脱碘酶可能在干细胞生物学和生理学的定义中发挥作用。干细胞具有无限的自我更新能力和分化为不同类型成熟细胞的潜力。解析所有这些事件是如何发生的,T3 信号如何在干细胞及其龛位中被控制和整合,以及它如何影响它们,这些基本上是未知的,也是未来几年的挑战。在这篇综述中,我将探讨脱碘酶在调节成年组织(如肌肉和肠道)干细胞中的 TH 信号中的作用,以及它们的作用如何控制自我更新、增殖和分化之间的微妙平衡。阐明甲状腺激素在干细胞中作用的分子机制可能揭示治疗潜力,例如在再生疾病和癌症领域。