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Oct-2 is required early in T cell-independent B cell activation for G1 progression and for proliferation.

作者信息

Corcoran L M, Karvelas M

机构信息

Walter and Eliza Hall Institute of Medical Research Post Office, Royal Melbourne Hospital, Victoria, Australia.

出版信息

Immunity. 1994 Nov;1(8):635-45. doi: 10.1016/1074-7613(94)90035-3.

DOI:10.1016/1074-7613(94)90035-3
PMID:7600291
Abstract

Oct-2, a POU homeodomain protein expressed primarily in B cells, is a powerful transcriptional activator that binds to DNA at sites appropriately placed for major effects on immunoglobulin gene expression. Our examination of B cell development and function in Oct-2 null mice did not support an essential role for Oct-2 early in B cell development. Rather, Oct-2 was required later, when B cells were induced to differentiate to antibody-secreting cells. We show here that Oct-2 is not required for normal immunoglobulin production by mature B lymphocytes. Instead, it is essential for a normal proliferative response to polyclonal mitogens. Responses to signals from activated T cells are unaffected. The requirement for Oct-2 maps to an early activation step in G1, during which B cells make the commitment to progress through the cell cycle and to divide.

摘要

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1
Oct-2 is required early in T cell-independent B cell activation for G1 progression and for proliferation.
Immunity. 1994 Nov;1(8):635-45. doi: 10.1016/1074-7613(94)90035-3.
2
oct-2 gene disruption eliminates the peritoneal B-1 lymphocyte lineage and attenuates B-2 cell maturation and function.八聚体转录因子2(Oct-2)基因缺失可消除腹膜B-1淋巴细胞谱系,并减弱B-2细胞的成熟和功能。
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J Immunol. 2004 Jan 15;172(2):1054-64. doi: 10.4049/jimmunol.172.2.1054.

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