Laboratory of Biomaterials, Institute for Frontier Life and Medical Sciences, Kyoto University, 53 Kawara-cho Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.
Sci Rep. 2018 Oct 4;8(1):14839. doi: 10.1038/s41598-018-33231-2.
The objective of this study is to prepare cationized gelatin nanospheres (cGNS) incorporating a molecular beacon (MB), and visualize cellular apoptosis. Two types of MB to detect the messenger RNA (mRNA) of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) (GAP MB), and caspase-3 (casp3 MB) were incorporated in cGNS, respectively. MB incorporated in cGNS showed the DNA sequence specificity in hybridization. The cGNS incorporation enabled MB to enhance the stability against nuclease to a significantly great extent compared with free MB. The cGNS incorporating GAP MB were internalized into the KUM6 of a mouse bone marrow-derived stem cell by an endocytotic pathway. The cGNS were not distributed at the lysosomes. After the incubation with cGNS, the cell apoptosis was induced at different concentrations of camptothecin. No change in the intracellular fluorescence was observed for cGNS. On the other hand, for the cGNS, the fluorescent intensity significantly enhanced by the apoptosis induction of cells. It is concluded that cGNS incorporating MB is a promising system for the visualization of cellular apoptosis.
本研究旨在制备阳离子化明胶纳米球(cGNS),并将分子信标(MB)整合其中,以可视化细胞凋亡。两种类型的 MB 分别被整合到 cGNS 中,用于检测甘油醛-3-磷酸脱氢酶(GAPDH)(GAP MB)和 caspase-3(casp3 MB)的信使 RNA(mRNA)。整合到 cGNS 中的 MB 在杂交中表现出 DNA 序列特异性。与游离 MB 相比,cGNS 的整合使 MB 的稳定性对核酸酶的抵抗力显著增强。GAP MB 整合的 cGNS 通过内吞途径被内化到小鼠骨髓来源干细胞的 KUM6 中。cGNS 不分布在溶酶体中。用 cGNS 孵育后,用不同浓度的喜树碱诱导细胞凋亡。cGNS 没有观察到细胞内荧光的变化。另一方面,对于 cGNS,随着细胞凋亡的诱导,荧光强度显著增强。因此,整合了 MB 的 cGNS 是可视化细胞凋亡的有前途的系统。