Sugiyama T, Yamamoto-Hino M, Miyawaki A, Furuichi T, Mikoshiba K, Hasegawa M
Tokyo Research Laboratories, Kyowa Hakko Kogyo Co., Japan.
FEBS Lett. 1994 Aug 1;349(2):191-6. doi: 10.1016/0014-5793(94)00662-8.
Inositol 1,4,5-trisphosphate (IP3)-mediated Ca2+ signaling plays important roles in cellular responses to extracellular stimuli. We recently succeeded in cloning human counterparts of the three subtypes derived from separate genes. Using the cDNA sequences type-specific to these subtype receptors, we here analyzed the expression profile of IP3R subtypes in stimulated and unstimulated human hematopoietic cell lines representing T cells, B cells, neutrophils, macrophages, erythrocytes and megakaryocytes. Northern and dot blot analysis showed that each IP3R subtype is expressed differently in these cells and that the expression profile in each cell is dynamically changed upon stimuli which induce differentiation. Moreover, most of these cells were found to simultaneously express at least two different subtype receptors.
肌醇1,4,5-三磷酸(IP3)介导的Ca2+信号传导在细胞对细胞外刺激的反应中起重要作用。我们最近成功克隆了源自不同基因的三种亚型的人类对应物。利用这些亚型受体特异的cDNA序列,我们在此分析了IP3R亚型在代表T细胞、B细胞、中性粒细胞、巨噬细胞、红细胞和巨核细胞的受刺激和未受刺激的人类造血细胞系中的表达谱。Northern印迹和斑点印迹分析表明,每种IP3R亚型在这些细胞中的表达不同,并且在诱导分化的刺激下,每个细胞中的表达谱会动态变化。此外,发现这些细胞中的大多数同时表达至少两种不同的亚型受体。