Quintans J, Kilkus J, McShan C L, Gottschalk A R, Dawson G
Department of Pathology, University of Chicago, IL 60637.
Biochem Biophys Res Commun. 1994 Jul 29;202(2):710-4. doi: 10.1006/bbrc.1994.1988.
We demonstrate for the first time how immature B cells kill themselves. Ceramide is identified as the mediator of apoptosis in the murine B lymphoma line WEHI 231 commonly used as a model to study clonal deletion in B lymphocytes. We show that exogenous ceramide induces apoptosis in WEHI 231 cells. To maintain self tolerance, immature lymphocytes readily undergo apoptotic death in response to the cross-linking of their antigen-specific receptors. We demonstrate that endogenously produced ceramide accumulates in WEHI 231 cells exposed to anti-IgM, an antigen surrogate before the onset of apoptosis. We also show that two other inducers of apoptosis, irradiation and dexamethasone, cause intracellular accumulation of ceramide.
我们首次证明了未成熟B细胞是如何自我毁灭的。神经酰胺被确定为鼠B淋巴瘤细胞系WEHI 231中细胞凋亡的介质,该细胞系通常被用作研究B淋巴细胞克隆缺失的模型。我们表明外源性神经酰胺可诱导WEHI 231细胞凋亡。为维持自身耐受性,未成熟淋巴细胞在其抗原特异性受体交联时会容易发生凋亡死亡。我们证明,在凋亡开始前,内源性产生的神经酰胺会在暴露于抗IgM(一种抗原替代物)的WEHI 231细胞中积累。我们还表明,另外两种细胞凋亡诱导剂,即辐射和地塞米松,会导致神经酰胺在细胞内积累。