Barbee Susannah D, Alberola-Ila José
Division of Biology, California Institute of Technology, 1200 E. California Boulevard, Mail code 147-75, Pasadena, CA 91125, USA.
Int Immunol. 2006 Jun;18(6):921-30. doi: 10.1093/intimm/dxl027. Epub 2006 Apr 24.
We have generated transgenic mice expressing the amino-terminal fragment of the phosphatidylinositol 3-kinase (PI3K) catalytic subunit (p110ABD) in thymocytes. Expression of p110ABD results in constitutive activation of PI3K and in significant increases in the numbers of mature, single-positive thymocytes. We previously reported that the increase in mature cells was in part due to a defect in thymic emigration. In this study we identify another component to this phenotype. Expression of p110ABD results in an enhancement of positive selection, without alterations in thymocyte lifespan or negative selection. Since PI3K can affect activation of Btk, which in turn potentiates calcium fluxes, during B cell development, our results suggest that PI3K could play a role in the regulation of Itk kinases in T cells, and that both cell types share a common signaling network to modulate calcium responses downstream of their antigen receptor.
我们已培育出在胸腺细胞中表达磷脂酰肌醇3激酶(PI3K)催化亚基氨基末端片段(p110ABD)的转基因小鼠。p110ABD的表达导致PI3K的组成性激活,并使成熟的单阳性胸腺细胞数量显著增加。我们之前报道过,成熟细胞数量的增加部分归因于胸腺迁出缺陷。在本研究中,我们确定了该表型的另一个组成部分。p110ABD的表达导致阳性选择增强,而胸腺细胞寿命或阴性选择没有改变。由于在B细胞发育过程中PI3K可影响Btk的激活,进而增强钙通量,我们的结果表明PI3K可能在T细胞中Itk激酶的调节中发挥作用,并且这两种细胞类型共享一个共同的信号网络来调节其抗原受体下游的钙反应。