Delille Hannah K, Dodt Gabriele, Schrader Michael
Centre for Cell Biology & Dept. of Biology; University of Aveiro; Aveiro, Portugal.
Commun Integr Biol. 2011 Jan;4(1):51-4. doi: 10.4161/cib.4.1.13647.
Peroxisomes are highly dynamic, multifunctional organelles that display remarkable changes in morphology, number and enzyme content. Peroxisomes multiply by growth and division of pre-existing organelles, but they can also form de novo from the ER. Growth and division of peroxisomes in mammalian cells involves elongation, membrane constriction and final fission and requires the peroxisome biogenesis Pex11 proteins as well as the recruitment of Dynamin-like protein DLP1/Drp1. We recently exploited the division-inhibiting properties of a unique Pex11pβ-YFP fusion protein to further dissect the process of peroxisomal growth and division. By applying life cell imaging and the HaloTag technology, our study revealed that Pex11pβ-mediated growth (elongation) and division of peroxisomes follows a multistep maturation pathway, which is initiated by the formation of an early peroxisomal membrane compartment from a pre-existing peroxisome and its stepwise conversion into a mature, metabolically active peroxisome compartment. Our observations support the view that peroxisomes formed by growth and division of pre-existing ones contain new membrane and matrix components. Peroxisome division is an asymmetric process, which is more complex than simple (symmetric) division of a preexisting organelle and equal distribution of the protein content. Our findings are in favor of Pex11pβ acting as a peroxisomal membrane shaping protein.
过氧化物酶体是高度动态的多功能细胞器,在形态、数量和酶含量方面表现出显著变化。过氧化物酶体通过已有细胞器的生长和分裂进行增殖,但它们也可以从内质网重新形成。哺乳动物细胞中过氧化物酶体的生长和分裂涉及伸长、膜收缩和最终裂变,需要过氧化物酶体生物发生Pex11蛋白以及动力蛋白样蛋白DLP1/Drp1的募集。我们最近利用一种独特的Pex11pβ-YFP融合蛋白的分裂抑制特性,进一步剖析过氧化物酶体生长和分裂的过程。通过应用活细胞成像和HaloTag技术,我们的研究表明,Pex11pβ介导的过氧化物酶体生长(伸长)和分裂遵循多步骤成熟途径,该途径由从已有过氧化物酶体形成早期过氧化物酶体膜区室并将其逐步转化为成熟的、具有代谢活性的过氧化物酶体区室启动。我们的观察结果支持这样一种观点,即由已有过氧化物酶体的生长和分裂形成的过氧化物酶体含有新的膜和基质成分。过氧化物酶体分裂是一个不对称过程,比已有细胞器的简单(对称)分裂和蛋白质含量的均匀分布更为复杂。我们的发现支持Pex11pβ作为过氧化物酶体膜塑形蛋白发挥作用。