Owen C S
Department of Biochemistry, Jefferson Medical College, Philadelphia.
Cell Calcium. 1988 Jun;9(3):141-7. doi: 10.1016/0143-4160(88)90017-6.
The calcium-responsive fluorescent dye indo-1 has been used in lymphocyte suspensions to measure changes in internal free calcium concentration, [Ca2+]i, in response to crosslinking of cell surface immunoglobulin. The quantitation of [Ca2+]i requires that indo-am ester used to load the cells be completely hydrolyzed to the indo-1 form inside the cells. This is shown to be greatly facilitated in the lymphocyte by the detergent Pluronic F-127. The quantitation of [Ca2+]i transients also requires an estimate of the fraction of the cells which contribute to the observed changes. The use of excessive amounts of intracellular dye can buffer [Ca2+]i transients and this effect has been used to estimate the size of the pool of calcium which is available for release when the B cell is stimulated by anti-immunoglobulin.
钙反应性荧光染料indo-1已用于淋巴细胞悬液中,以测量细胞内游离钙浓度[Ca2+]i的变化,该变化是对细胞表面免疫球蛋白交联的反应。[Ca2+]i的定量要求用于加载细胞的indo-1酯在细胞内完全水解为indo-1形式。结果表明,去污剂普朗尼克F-127能极大地促进淋巴细胞中的这种水解。[Ca2+]i瞬变的定量还需要估计对观察到的变化有贡献的细胞比例。使用过量的细胞内染料可以缓冲[Ca2+]i瞬变,这种效应已被用于估计当B细胞受到抗免疫球蛋白刺激时可释放的钙池大小。