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羟基磷灰石的促有丝分裂活性:对生长调节素C的需求。

Mitogenic activity of hydroxyapatite: requirement for somatomedin C.

作者信息

Cheung H S, Van Wyk J J, Russell W E, McCarty D J

出版信息

J Cell Physiol. 1986 Aug;128(2):143-8. doi: 10.1002/jcp.1041280202.

Abstract

Synovial hyperplasia is a feature of the chronic synovitis associated with basic calcium phosphate crystals [hydroxyapatite (HA), octacalcium phosphate, tricalcium phosphate] and calcium pyrophosphate. Each of these crystals stimulated mitosis of cultured human skin fibroblasts or canine synovial fibroblasts in a concentration-dependent fashion. We examined the effect of pure somatomedin C (Sm-C) on HA crystal induced mitogenesis. Confluent cultures of human fibroblasts were rendered quiescent by incubation in the presence of 1% platelet-poor-Sm-C free plasma (PPSCFP) for 24 hours. HA crystals stimulated thymidine incorporation 2.3-fold over control value. Addition of Sm-C significantly augmented the effect of HA crystals (P less than 0.01). Nearly identical effects were observed in the presence of 100 micrograms/ml HA crystals or 15 ng/ml PDGF. Monoclonal antibodies against Sm-C had little effect on the basal 3H thymidine uptake by control cells incubated in 1% PPSCFP but blocked over 50% of the HA crystal or PDGF-induced 3H thymidine incorporation both in the presence or absence of Sm-C. The incomplete blocking suggested either the presence of other "progression" factors, such as insulin-like growth factor II in the conditioned media or the possibility that HA or PDGF in high enough dosage enabled cells to escape their dependence on Sm-C for DNA synthesis.

摘要

滑膜增生是与碱性磷酸钙晶体(羟基磷灰石、磷酸八钙、磷酸三钙)和焦磷酸钙相关的慢性滑膜炎的一个特征。这些晶体中的每一种都以浓度依赖的方式刺激培养的人皮肤成纤维细胞或犬滑膜成纤维细胞的有丝分裂。我们研究了纯生长调节素C(Sm-C)对羟基磷灰石晶体诱导的有丝分裂的影响。人成纤维细胞的汇合培养物在含有1%无血小板Sm-C的无血浆(PPSCFP)中孵育24小时后进入静止状态。羟基磷灰石晶体刺激的胸苷掺入量比对照值高2.3倍。添加Sm-C显著增强了羟基磷灰石晶体的作用(P小于0.01)。在存在100微克/毫升羟基磷灰石晶体或15纳克/毫升血小板衍生生长因子(PDGF)的情况下观察到几乎相同的效果。抗Sm-C单克隆抗体对在1%PPSCFP中孵育的对照细胞的基础3H胸苷摄取几乎没有影响,但在有或没有Sm-C的情况下,都能阻断超过50%的羟基磷灰石晶体或PDGF诱导的3H胸苷掺入。这种不完全阻断表明,要么条件培养基中存在其他“促进”因子,如胰岛素样生长因子II,要么高剂量的羟基磷灰石或PDGF使细胞能够摆脱对Sm-C进行DNA合成的依赖。

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