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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Cellular internalization of rod-like nano hydroxyapatite particles and their size and dose-dependent effects on pre-osteoblasts
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Cellular internalization of rod-like nano hydroxyapatite particles and their size and dose-dependent effects on pre-osteoblasts

机译:棒状纳米羟基磷灰石颗粒的细胞内化及其大小和剂量依赖性对成骨细胞的影响

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摘要

Nano hydroxyapatite particles (n-HA) have been reported to promote osteogenic activities of bonerelated cells, while inhibiting tumor cell growth, and the biological effects of n-HA are related with the particle size, dose, culture time and cell type. In this work, we prepared n-HA with a strictly controlled rod-like shape and adjustable sizes without any surface chemical contaminations. Using the prepared n-HA, we investigated the size and dose effect of the nano particles on pre-osteoblasts for up to 7 days. We probed cell proliferation and gene expression in the presence of n-HA, the cellular uptake pathways of n-HA particles, as well as the extracellular and intracellular [Ca2+] ([Ca2+](i)) changes caused by the particles, in order to get a better understanding of the biological effects of n-HA of various sizes. The n-HA exhibited size-and dose-dependent impacts on MC3T3-E1 proliferation, intracellular reactive oxygen species (ROS) generation, mitochondrial membrane potential, and osteogenic gene expression. 40 nm n-HA caused the slowest MC3T3-E1 growth, the highest intracellular ROS concentration, the largest mitochondrial membrane potential loss and the lowest level of osteogenic gene expression among the samples. The cytotoxicity of 40 nm n-HA increased with the dose and culture time. 70 nm n-HA showed beneficial effects on MC3T3-E1 growth, but the positive effect disappeared at the highest concentration on day 7. 100 nm n-HA promoted cell growth and the promoting effect increased with the dose. Cells cultured with 100 nm n-HA expressed the highest level of osteogenic gene expression among the experimental groups. We discovered that the presence of n-HA increased [Ca2+] i but did not elevate extracellular [Ca2+]. The [Ca2+] i increased as the n-HA size decreased. We also found that n-HA may enter cells through two pathways and that the amount of engulfed particles depended on the particle size. The internalized n-HA particles located in the cytosol, endosomes, lysosomes and nuclei. The particles dissolved in lysosomes and raised [Ca2+] i, which correlated with the cell death and osteogenic gene expression. In conclusion, the particle size, dose, and culture time influenced the biological effects of n-HA on ME3T3-E1 cells, probably by changing the [Ca2+] i in the cells instead of the extracellular [Ca2+].
机译:据报道,纳米羟基磷灰石颗粒(n-HA)可促进骨相关细胞的成骨活性,同时抑制肿瘤细胞生长,其生物学效应与颗粒大小、剂量、培养时间和细胞类型有关。在这项工作中,我们制备的n-HA具有严格控制的棒状形状和可调节的尺寸,没有任何表面化学污染。使用制备的n-HA,我们研究了纳米颗粒对前成骨细胞的大小和剂量效应长达7天。我们研究了n-HA存在下的细胞增殖和基因表达,n-HA颗粒的细胞摄取途径,以及颗粒引起的细胞外和细胞内[Ca2+]([Ca2+](i))变化,以便更好地了解各种大小的n-HA的生物学效应。n-HA对MC3T3-E1增殖、细胞内活性氧(ROS)生成、线粒体膜电位和成骨基因表达具有大小和剂量依赖性影响。在这些样本中,40 nm n-HA导致MC3T3-E1生长最慢,细胞内ROS浓度最高,线粒体膜电位损失最大,成骨基因表达水平最低。40nm n-HA的细胞毒性随着剂量和培养时间的增加而增加。70nm n-HA对MC3T3-E1的生长显示出有益的作用,但在第7天的最高浓度下,这种积极作用消失。100nm n-HA促进细胞生长,且促进作用随剂量增加而增强。在实验组中,用100nm n-HA培养的细胞表达的成骨基因水平最高。我们发现,n-HA的存在增加了[Ca2+]i,但没有提高细胞外[Ca2+]。[Ca2+]i随着n-HA尺寸的减小而增加。我们还发现,n-HA可能通过两种途径进入细胞,被吞噬颗粒的数量取决于颗粒大小。内化的n-HA颗粒位于细胞质、内体、溶酶体和细胞核中。颗粒溶解在溶酶体中并升高[Ca2+]i,这与细胞死亡和成骨基因表达有关。总之,粒径、剂量和培养时间可能通过改变细胞内[Ca2+]i而不是细胞外[Ca2+]i来影响n-HA对ME3T3-E1细胞的生物学效应。

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