Quong Melanie W, Romanow William J, Murre Cornelis
Division of Biology, University of California, San Diego, 9500 Gilman Drive, MC 0366, La Jolla, California 92093-0366, USA.
Annu Rev Immunol. 2002;20:301-22. doi: 10.1146/annurev.immunol.20.092501.162048. Epub 2001 Oct 4.
Lymphocytes arise from hematopoietic stem cells through the coordinated action of transcription factors. The E proteins (E12, E47, HEB and E2-2) have emerged as key regulators of both B and T lymphocyte differentiation. This review summarizes the current data and examines the various functions of E proteins and their antagonists, Id2 and Id3, throughout lymphoid maturation. Beyond an established role in B and T lineage commitment, E proteins continue to be essential at subsequent stages of development. E protein activity regulates the expression of surrogate and antigen receptor genes, promotes Ig and TCR rearrangements, and coordinates cell survival and proliferation with developmental progression in response to TCR signaling. Finally, this review also discusses the role of E47 as a tumor suppressor.
淋巴细胞通过转录因子的协同作用从造血干细胞产生。E蛋白(E12、E47、HEB和E2-2)已成为B和T淋巴细胞分化的关键调节因子。本综述总结了当前数据,并研究了E蛋白及其拮抗剂Id2和Id3在整个淋巴细胞成熟过程中的各种功能。除了在B和T细胞谱系定向中的既定作用外,E蛋白在随后的发育阶段仍然至关重要。E蛋白活性调节替代受体和抗原受体基因的表达,促进Ig和TCR重排,并响应TCR信号与发育进程协调细胞存活和增殖。最后,本综述还讨论了E47作为肿瘤抑制因子的作用。