A novel role for microtubules in apoptotic chromatin dynamics and cellular fragmentation

• Published in: Journal of cell science Vol. 119; no. Pt 11; pp. 2362 - 2374
• Main Authors: Moss, David K, Betin, Virginie M, Malesinski, Soazig D, Lane, Jon D
• Format: Journal Article
• Language: English
• Published: England Company of Biologists 01.06.2006
• Subjects: Anisomycin - pharmacology; Apoptosis - drug effects; Apoptosis - physiology; Apoptosis - radiation effects; Biochemistry; Biochemistry, Molecular Biology; Cell Line; Cellular Biology; Chromatin - metabolism; HeLa Cells; Humans; Life Sciences; Macrophages - metabolism; Microscopy, Fluorescence - methods; Microtubules - physiology; Pharmaceutical sciences; Ultraviolet Rays
• ISSN: 0021-9533; 1477-9137
• DOI: 10.1242/jcs.02959

Dramatic changes in cellular dynamics characterise the apoptotic execution phase, culminating in fragmentation into membrane-bound apoptotic bodies. Previous evidence suggests that actin-myosin plays a dominant role in apoptotic cellular remodelling, whereas all other cytoskeletal elements dismantle. We have used fixed cells and live-cell imaging to confirm that interphase microtubules rapidly depolymerise at the start of the execution phase. Around this time, pericentriolar components (pericentrin, ninein and gamma-tubulin) are lost from the centrosomal region. Subsequently, however, extensive non-centrosomal bundles of densely packed, dynamic microtubules rapidly assemble throughout the cytoplasm in all cell lines tested. These microtubules have an important role in the peripheral relocation of chromatin in the dying cell, because nocodazole treatment restricts the dispersal of condensed apoptotic chromatin into surface blebs, and causes the withdrawal of chromatin fragments back towards the cell centre. Importantly, nocodazole and taxol are both potent inhibitors of apoptotic fragmentation in A431 cells, implicating dynamic microtubules in apoptotic body formation. Live-cell-imaging studies indicate that fragmentation is accompanied by the extension of rigid microtubule-rich spikes that project through the cortex of the dying cell. These structures enhance interactions between apoptotic cells and phagocytes in vitro, by providing additional sites for attachment to neighbouring cells.