Tsukamoto Satoshi, Hara Taichi, Yamamoto Atsushi, Ohta Yuki, Wada Ayako, Ishida Yuka, Kito Seiji, Nishikawa Tetsu, Minami Naojiro, Sato Ken, Kokubo Toshiaki
Laboratory Animal and Genome Sciences Section, National Institute of Radiological Sciences, Chiba 263-8555, Japan.
J Reprod Dev. 2013;59(1):33-9. doi: 10.1262/jrd.2012-096. Epub 2012 Oct 19.
Lysosomes are acidic and highly dynamic organelles that are essential for macromolecule degradation and many other cellular functions. However, little is known about lysosomal function during early embryogenesis. Here, we found that the number of lysosomes increased after fertilization. Lysosomes were abundant during mouse preimplantation development until the morula stage, but their numbers decreased slightly in blastocysts. Consistently, the protein expression level of mature cathepsins B and D was high from the one-cell to morula stages but low in the blastocyst stage. One-cell embryos injected with siRNAs targeted to both lysosome-associated membrane protein 1 and 2 (LAMP1 and LAMP2) were developmentally arrested at the two-cell stage. Pharmacological inhibition of lysosomes also caused developmental retardation, resulting in accumulation of lipofuscin. Our findings highlight the functional changes in lysosomes in mouse preimplantation embryos.
溶酶体是酸性且高度动态的细胞器,对大分子降解及许多其他细胞功能至关重要。然而,关于早期胚胎发育过程中溶酶体的功能却知之甚少。在此,我们发现受精后溶酶体数量增加。在小鼠植入前发育阶段直至桑椹胚期,溶酶体数量丰富,但在囊胚期其数量略有减少。同样,成熟组织蛋白酶B和D的蛋白质表达水平在单细胞期至桑椹胚期较高,而在囊胚期较低。注射针对溶酶体相关膜蛋白1和2(LAMP1和LAMP2)的小干扰RNA(siRNA)的单细胞胚胎在二细胞期发育停滞。对溶酶体的药理学抑制也导致发育迟缓,从而导致脂褐素积累。我们的研究结果突出了小鼠植入前胚胎中溶酶体的功能变化。