Richter J, Olsson I, Andersson T
Department of Medicine, University Hospital, Lund, Sweden.
J Biol Chem. 1990 Aug 25;265(24):14358-63.
By using a hemolytic plaque assay to detect release of lactoferrin and myeloperoxidase, tumor necrosis factor (TNF) was shown previously to induce secretion of these granule proteins from single adherent neutrophils. Secretion was inhibited by loading neutrophils with calcium chelators, indicating a crucial role of cytosolic free [Ca2+] in the signal transduction mechanism of TNF. In the present study, using a microfluorometer technique to follow changes in the cytosolic free [Ca2+] in single adherent neutrophils, we were not able to detect any TNF-induced [Ca2+] transients. However, these adherent cells exhibited spontaneous oscillations of their cytosolic free [Ca2+], as previously reported (Jaconi, M.E.E., Rivest, R.W., Schlegel, W., Wollheim, C.B., Pittet, D., and Lew, P.D. (1988) J. Biol. Chem. 263, 10557-10560). A close correlation was found between a reduced oscillatory activity of cytosolic free [Ca2+] and a reduced ability of TNF to induce degranulation, by reducing the extracellular [Ca2+] or loading the cells with a calcium chelator (1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid). In addition, when the cells were incubated at 37 degrees C for 3 h there was a parallel decline in the spontaneous oscillatory activity of cytosolic free [Ca2+] and TNF-induced secretion of lactoferrin. Control experiments showed that phorbol 12-myristate 13-acetate-induced secretion was not affected under the same conditions, indicating that the secretory process per se was not disturbed. We conclude that TNF by itself does not give rise to any changes of the cytosolic free [Ca2+] but that the spontaneous oscillatory activity of cytosolic free [Ca2+] in adherent neutrophils is necessary for TNF-induced degranulation.
通过使用溶血空斑试验来检测乳铁蛋白和髓过氧化物酶的释放,先前研究表明肿瘤坏死因子(TNF)可诱导这些颗粒蛋白从单个贴壁中性粒细胞中分泌。用钙螯合剂处理中性粒细胞可抑制分泌,这表明胞质游离[Ca2+]在TNF的信号转导机制中起关键作用。在本研究中,我们使用微量荧光计技术跟踪单个贴壁中性粒细胞中胞质游离[Ca2+]的变化,却未能检测到任何TNF诱导的[Ca2+]瞬变。然而,这些贴壁细胞表现出其胞质游离[Ca2+]的自发振荡,正如先前报道的那样(Jaconi, M.E.E., Rivest, R.W., Schlegel, W., Wollheim, C.B., Pittet, D., and Lew, P.D. (1988) J. Biol. Chem. 263, 10557 - 10560)。通过降低细胞外[Ca2+]或用钙螯合剂(1,2 - 双(2 - 氨基苯氧基)乙烷 - N,N,N',N' - 四乙酸)处理细胞,发现胞质游离[Ca2+]振荡活性降低与TNF诱导脱颗粒的能力降低之间存在密切相关性。此外,当细胞在37℃孵育3小时时,胞质游离[Ca2+]的自发振荡活性和TNF诱导的乳铁蛋白分泌平行下降。对照实验表明,在相同条件下佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯诱导的分泌不受影响,这表明分泌过程本身未受干扰。我们得出结论,TNF本身不会引起胞质游离[Ca2+]的任何变化,但贴壁中性粒细胞中胞质游离[Ca2+]的自发振荡活性是TNF诱导脱颗粒所必需的。