首页> 外文期刊>Acta biomaterialia >Effects of micrometric titanium particles on osteoblast attachment and cytoskeleton architecture.
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Effects of micrometric titanium particles on osteoblast attachment and cytoskeleton architecture.

机译:微米级钛颗粒对成骨细胞附着和细胞骨架结构的影响。

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摘要

Titanium (Ti) and its alloys are widely used in biomedical devices as bone tissue replacements due to their advantageous bulk mechanical properties and biocompatibility. It is known that particles released from Ti-based implants impair essential functions of osteoblasts, which for survival require attachment to specific extracellular matrix proteins at the bone surface. This study investigates whether Ti particles of micrometric sizes affect the osteoblast attachment machinery. Exposure of human osteoblastic Saos-2 cells to Ti particles impaired their adhesion strength, migration and proliferation. Attenuation of these functions was associated with reduced cell spreading, cell membrane disruptions and loss of cell shape. Cell exposure to Ti particles led to changes in cytoskeletal structures, including reduced ventral stress fibers combined with a disorderly arrangement of beta-tubulin and acetylated alpha-tubulin fibers. Cytoskeleton disassembly was associated with a reduction in overall cell adhesion area, characterized by fewer centrally localized focal adhesions and shorter focal contacts at the periphery. Paxillin adaptor protein redistributed to peripheral corner regions, colocalizing with poorly organized actin fibers at attachment sites. Total focal adhesion kinase (FAK) protein amounts, as well as its degree of phosphorylation on the active form p-FAK (Tyr-397), decreased, which was accompanied by a lesser extent of co-localization with paxillin in focal contacts. On the other hand, p-FAK (Tyr-407), an inhibitory form of FAK, accumulated in the focal contacts of Ti-treated cells. Pyk2 phosphorylated on Tyr-402 colocalized with paxillin in focal contacts of untreated cells, while it was barely detected upon exposure to particles. In summary, changes in the phosphorylation states of both FAK and Pyk2 tyrosine kinases at focal contacts underlie impaired bone-forming cell attachment after exposure to Ti particles of micrometric sizes.
机译:钛(Ti)及其合金由于其有利的整体机械性能和生物相容性而广泛用于生物医学设备中,作为骨组织的替代品。众所周知,从钛基植入物中释放的颗粒会损害成骨细胞的基本功能,成骨细胞的生存需要在骨表面附着特定的细胞外基质蛋白。这项研究调查了微米尺寸的钛颗粒是否会影响成骨细胞的附着机制。人成骨细胞Saos-2细胞暴露于Ti颗粒会削弱其粘附强度,迁移和增殖。这些功能的减弱与细胞扩散减少,细胞膜破裂和细胞形状丧失有关。细胞暴露于Ti颗粒会导致细胞骨架结构发生变化,包括腹侧应力纤维减少以及无序排列的β-微管蛋白和乙酰化的α-微管蛋白纤维。细胞骨架的拆卸与总体细胞粘附面积的减少有关,其特征在于较少的中央局部粘着粘附和较短的在周围的粘着接触。 Paxillin衔接蛋白重新分布到周围的角区域,在附着位点与组织不良的肌动蛋白纤维共定位。总的粘着斑激酶(FAK)蛋白含量及其在活性形式p-FAK(Tyr-397)上的磷酸化程度降低,伴随着在局部接触中与Paxillin共定位的程度降低。另一方面,p-FAK(Tyr-407)是FAK的一种抑制形式,积累在Ti处理的细胞的焦点接触中。在Tyr-402上磷酸化的Pyk2与未处理细胞的焦点接触中的Paxillin共定位,而在暴露于颗粒时几乎未检测到。总之,在暴露于微米级尺寸的Ti颗粒后,焦点接触处FAK和Pyk2酪氨酸激酶的磷酸化状态的改变是成骨细胞附着受损的基础。

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