Institute of Laboratory Animal Science, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
Genes (Basel). 2011 Mar 9;2(1):280-97. doi: 10.3390/genes2010280.
Developmental biology, regenerative medicine and cancer biology are more and more interested in understanding the molecular mechanisms controlling pluripotency and self-renewal in stem cells. Pluripotency is maintained by a synergistic interplay between extrinsic stimuli and intrinsic circuitries, which allow sustainment of the undifferentiated and self-renewing state. Nevertheless, even though a lot of efforts have been made in the past years, the precise mechanisms regulating these processes remain unclear. One of the key extrinsic factors is leukemia inhibitory factor (LIF) that is largely used for the cultivation and derivation of mouse embryonic and induced pluripotent stem cells. LIF acts through the LIFR/gp130 receptor and activates STAT3, an important regulator of mouse embryonic stem cell self-renewal. STAT3 is known to inhibit differentiation into both mesoderm and endoderm lineages by preventing the activation of lineage-specific differentiation programs. However, LIF activates also parallel circuitries like the PI3K-pathway and the MEK/ERK-pathway, but its mechanisms of action remain to be better elucidated. This review article aims at summarizing the actual knowledge on the importance of LIF in the maintenance of pluripotency and self-renewal in embryonic and induced pluripotent stem cells.
发育生物学、再生医学和癌症生物学越来越有兴趣了解控制干细胞多能性和自我更新的分子机制。多能性是通过外在刺激和内在电路的协同相互作用来维持的,这种相互作用允许维持未分化和自我更新的状态。然而,尽管过去几年已经做了很多努力,但调节这些过程的确切机制仍不清楚。一个关键的外在因素是白血病抑制因子(LIF),它被广泛用于培养和衍生小鼠胚胎和诱导多能干细胞。LIF 通过 LIFR/gp130 受体发挥作用,并激活 STAT3,这是小鼠胚胎干细胞自我更新的重要调节剂。STAT3 通过阻止谱系特异性分化程序的激活,已知可抑制向中胚层和内胚层谱系的分化。然而,LIF 还激活了类似 PI3K 通路和 MEK/ERK 通路的平行通路,但它的作用机制仍有待更好地阐明。本文旨在总结 LIF 在维持胚胎和诱导多能干细胞的多能性和自我更新中的重要性的现有知识。