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Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/41481
Title: Apoptotic microtubule network organization and maintenance depend on high cellular ATP levels and energized mitochondria
Authors: Oropesa-Ávila, Manuel; Mata, Mario de la; Garrido-Maraver, Juan; Cordero, Mario D.; Cotán, David; Rodríguez-Hernández, Ángeles; Domínguez-Moñino, Irene ; Miguel, Manuel de; Navas, Plácido; Sánchez-Alcázar, José Antonio
Keywords: Apoptosis
Mitochondria membrane potential
Issue Date: 10-Feb-2011
Publisher: Springer
Citation: Apoptosis 16(4): 404-424 (2011)
Abstract: Microtubule cytoskeleton is reformed during apoptosis, forming a cortical structure beneath plasma membrane, which plays an important role in preserving cell morphology and plasma membrane integrity. However, the maintenance of the apoptotic microtubule network (AMN) during apoptosis is not understood. In the present study, we examined apoptosis induced by camptothecin (CPT), a topoisomerase I inhibitor, in human H460 and porcine LLCPK-1α cells. We demonstrate that AMN was organized in apoptotic cells with high ATP levels and hyperpolarized mitochondria and, on the contrary, was dismantled in apoptotic cells with low ATP levels and mitochondrial depolarization. AMN disorganization after mitochondrial depolarization was associated with increased plasma membrane permeability assessed by enhancing LDH release and increased intracellular calcium levels. Living cell imaging monitoring of both, microtubule dynamics and mitochondrial membrane potential, showed that AMN persists during apoptosis coinciding with cycles of mitochondrial hyperpolarization. Eventually, AMN was disorganized when mitochondria suffered a large depolarization and cell underwent secondary necrosis. AMN stabilization by taxol prevented LDH release and calcium influx even though mitochondria were depolarized, suggesting that AMN is essential for plasma membrane integrity. Furthermore, high ATP levels and mitochondria polarization collapse after oligomycin treatment in apoptotic cells suggest that ATP synthase works in “reverse” mode during apoptosis. These data provide new explanations for the role of AMN and mitochondria during apoptosis.
Description: 22 páginas, 15 figuras.
Publisher version (URL): http://dx.doi.org/10.1007/s10495-011-0577-1
URI: http://hdl.handle.net/10261/41481
DOI: 10.1007/s10495-011-0577-1
ISSN: 1360-8185
E-ISSN: 1573-675X
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