Murgia M, Pizzo P, Steinberg T H, Di Virgilio F
C.N.R. Center for the Study of the Physiology of Mitochondria, University of Padova, Italy.
Biochem J. 1992 Dec 15;288 ( Pt 3)(Pt 3):897-901. doi: 10.1042/bj2880897.
Extracellular ATP (ATPo) is known to be cytotoxic to many cell types through a mechanism which is largely unknown. Very recently this nucleotide has been shown to cause cell death by apoptosis, probably by interacting with specific cell-surface receptors. In the present study we have investigated the mechanism of ATPo-dependent cytotoxicity in the macrophage-like mouse cell line J774. It has been previously reported that in this cell type ATPo activates trans-membrane Ca2+ and Na+ fluxes and a drastic increase in the plasma-membrane permeability to hydrophilic solutes smaller than 900 Da. These changes are followed by cell swelling and lysis. We show in the present study that, although this nucleotide triggers a rise in the cytoplasmic Ca2+ concentration, neither cell swelling nor lysis is Ca(2+)-dependent. Furthermore, cell lysis is not dependent on Na+ influx, as it is not prevented by iso-osmotic replacement of extracellular Na+ with choline or N-methylglucamine. On the contrary, ATPo-dependent cytotoxicity, but not the ATPo-dependent increase in plasma-membrane permeability, is completely abrogated in sucrose medium. Under our experimental conditions ATPo does not cause DNA fragmentation in J774 cells. We conclude from these findings that ATPo does not cause apoptosis of J774 macrophages and promotes a Ca(2+)- and Na(+)-independent colloido-osmotic lysis.
细胞外ATP(ATPo)已知通过一种很大程度上未知的机制对多种细胞类型具有细胞毒性。最近,这种核苷酸已被证明可通过凋亡导致细胞死亡,可能是通过与特定的细胞表面受体相互作用。在本研究中,我们研究了巨噬细胞样小鼠细胞系J774中ATPo依赖性细胞毒性的机制。先前已有报道,在这种细胞类型中,ATPo可激活跨膜Ca2+和Na+通量,并使质膜对小于900 Da的亲水性溶质的通透性急剧增加。这些变化随后会导致细胞肿胀和裂解。我们在本研究中表明,尽管这种核苷酸会引发细胞质Ca2+浓度升高,但细胞肿胀和裂解均不依赖于Ca(2+)。此外,细胞裂解不依赖于Na+内流,因为用胆碱或N-甲基葡糖胺等渗替代细胞外Na+并不能阻止细胞裂解。相反,在蔗糖培养基中,ATPo依赖性细胞毒性完全消除,但ATPo依赖性的质膜通透性增加并未消除。在我们的实验条件下,ATPo不会导致J774细胞中的DNA片段化。我们从这些发现中得出结论,ATPo不会导致J774巨噬细胞凋亡,而是促进一种不依赖于Ca(2+)和Na(+)的胶体渗透压裂解。