Zhou Chen, Yang Guodong, Chen Mo, He Ling, Xiang Lusai, Ricupero Christopher, Mao Jeremy J, Ling Junqi
*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China.
*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China
FASEB J. 2015 Oct;29(10):4083-91. doi: 10.1096/fj.14-267500. Epub 2015 Jul 6.
As transcription factors of the lines (LIN)-11/Islet (Isl)-1/mitosis entry checkpoint (MEC)-3 (LIM)-homeobox subfamily, LIM homeobox (Lhx)6 and -8 are remarkably conserved and involved in the morphogenesis of multiple organ systems. Lhx6 and -8 play overlapping and distinctive roles, but in general act as cell fate mediators and in turn are regulated by several transcriptional factors, such as sonic hedgehog, fibroblast growth factors, and wingless-int (Wnt)/β-catenin. In this review, we first summarize Lhx6 and -8 distributions in development and then explore how Lhx6 and -8 act as transcription factors and coregulators of cell lineage specification. Known Lhx6 and -8 functions and targets are outlined in neurogenesis, craniofacial development, and germ cell differentiation. The underlying mechanisms of Lhx6 and -8 in regulating cell fate remain elusive. Whether Lhx6 and -8 affect functions in tissues and organs other than neural, craniofacial, oocytes, and germ cells is largely unexplored. Taken together, Lhx6 and -8 are important regulators of cell lineage specification and may act as one of the pivotal mediators of stem cell fate. Undoubtedly, future investigations of Lhx6 and -8 biology will continue to yield fascinating insights into tissue development and homeostasis, in addition to their putative roles in tissue regeneration and ageing.
作为LIN-11/胰岛(Isl)-1/有丝分裂进入检查点(MEC)-3(LIM)同源框亚家族的转录因子,LIM同源框(Lhx)6和-8具有高度保守性,并参与多个器官系统的形态发生。Lhx6和-8发挥着重叠且独特的作用,但总体上作为细胞命运的调节因子,反过来又受多种转录因子调控,如音猬因子、成纤维细胞生长因子和无翅型MMTV整合位点家族(Wnt)/β-连环蛋白。在本综述中,我们首先总结Lhx6和-8在发育过程中的分布,然后探讨Lhx6和-8如何作为转录因子以及细胞谱系特化的共调节因子发挥作用。已知的Lhx6和-8在神经发生、颅面发育和生殖细胞分化中的功能及靶点也在文中进行了概述。Lhx6和-8调控细胞命运的潜在机制仍不清楚。Lhx6和-8是否会影响除神经、颅面、卵母细胞和生殖细胞以外的组织和器官的功能,在很大程度上尚未得到探索。综上所述,Lhx6和-8是细胞谱系特化的重要调节因子,可能是干细胞命运的关键调节因子之一。毫无疑问,未来对Lhx6和-8生物学特性的研究,除了它们在组织再生和衰老中的假定作用外,将继续为组织发育和内稳态带来迷人的见解。