Anastasia Luigi, Papini Nadia, Colazzo Francesca, Palazzolo Giacomo, Tringali Cristina, Dileo Loredana, Piccoli Marco, Conforti Erika, Sitzia Clementina, Monti Eugenio, Sampaolesi Maurilio, Tettamanti Guido, Venerando Bruno
Department of Medical Chemistry, Biochemistry, and Biotechnology, University of Milan, 20090 Milan, Italy.
J Biol Chem. 2008 Dec 26;283(52):36265-71. doi: 10.1074/jbc.M805755200. Epub 2008 Oct 22.
Membrane-bound sialidase NEU3, often referred to as the "ganglioside sialidase," has a critical regulatory function on the sialoglycosphingolipid pattern of the cell membrane, with an anti-apoptotic function, especially in cancer cells. Although other sialidases have been shown to be involved in skeletal muscle differentiation, the role of NEU3 had yet to be disclosed. Herein we report that NEU3 plays a key role in skeletal muscle differentiation by strictly modulating the ganglioside content of adjacent cells, with special regard to GM3. Induced down-regulation of NEU3 in murine C2C12 myoblasts, even when partial, totally inhibits their capability to differentiate by increasing the GM3 level above a critical point, which causes epidermal growth factor receptor inhibition (and ultimately its down-regulation) and an higher responsiveness of myoblasts to the apoptotic stimuli.
膜结合唾液酸酶NEU3,常被称为“神经节苷脂唾液酸酶”,对细胞膜的唾液酸糖鞘脂模式具有关键的调节功能,并具有抗凋亡功能,尤其是在癌细胞中。尽管其他唾液酸酶已被证明参与骨骼肌分化,但NEU3的作用尚未被揭示。在此我们报告,NEU3通过严格调节相邻细胞的神经节苷脂含量,特别是GM3,在骨骼肌分化中起关键作用。在小鼠C2C12成肌细胞中诱导NEU3下调,即使是部分下调,也会通过将GM3水平提高到临界点以上,完全抑制其分化能力,这会导致表皮生长因子受体抑制(最终导致其下调)和成肌细胞对凋亡刺激的更高反应性。