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使用藻酸盐珠培养的兔关节软骨细胞对软骨降解进行组织形态计量学评估——透明质酸的作用。

Histomorphometric Evaluation of Cartilage Degradation using Rabbit Articular Chondrocytes Cultured in Alginate Beads - Effects of Hyaluronan.

作者信息

Nakatsuka K, Kurita K, Hayakawa Taro, Nakashima Katsuhito, Yamashita Kyoko, Hoshino Takeshi, Miyazaki Kyosuke

机构信息

Department of Oral and Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin Unuverity, Japan;

出版信息

Int J Biomed Sci. 2010 Jun;6(2):103-10.

Abstract

OBJECTIVE

A 3-dimensional alginate bead culturing method using rabbit articular chondrocytes was studied for the screening of the effectiveness of drugs for articular diseases.

DESIGN

The beads cultured with IL-1β, TGF-β, and Hyaluronan (HA) were evaluated histochemically with Alecian blue and immunohistochemically with CS-56 antibody. Chondrocytes in alginate beads were arbitrarily classified into four groups: 1) chodrocyte surrounded with cell-associated matrix (CAM) in which proteoglycan (PG) was positively stained (PG-possitive chondrocyte); 2) chondrocyte with PG-negative CAM; 3) PG-positive CAM alone, and 4) PG-negative CAM alone. Total sulfated GAG concentrations in the culture media were quantitated by dimethylmethylene blue (DMMB) assay. ProMMP-3, TIMP-1 and -2 concentrations in the culture media were determined by sandwich enzyme immunoassays.

RESULTS

Significant increase of PG-nagative cells were immunohistochemically found by IL-1β stimulation. The pretreatment with TGF-β almost fully suppressed those increase of PG-negative cells by IL-1β. Both GAG and proMMP-3 concentrations in the culture media were significantly increased after IL-1β stimulation. There were no significant differences in both TIMP-1 and TIMP-2 concentrations in the culture media with or without IL-1β stimulation. 800-kDa HA reduced significantly the number of PG-negative cells and proMMP-3 concentration in the culture media, but showed no effects on the concentrations of both TIMPs.

CONCLUSIONS

Because this 3-dimensional chondrocyte culture in alginate beads is close to in vivo conditions, this method can be used for evaluation of the effectiveness of novel drugs for articular diseases.

摘要

目的

研究一种使用兔关节软骨细胞的三维藻酸盐珠培养方法,用于筛选治疗关节疾病药物的有效性。

设计

用白细胞介素-1β(IL-1β)、转化生长因子-β(TGF-β)和透明质酸(HA)培养的珠子,采用阿利新蓝进行组织化学评估,并用CS-56抗体进行免疫组织化学评估。藻酸盐珠中的软骨细胞被任意分为四组:1)被细胞相关基质(CAM)包围的软骨细胞,其中蛋白聚糖(PG)呈阳性染色(PG阳性软骨细胞);2)PG阴性CAM的软骨细胞;3)单独的PG阳性CAM;4)单独的PG阴性CAM。通过二甲基亚甲基蓝(DMMB)测定法定量培养基中总硫酸化糖胺聚糖(GAG)的浓度。通过夹心酶免疫测定法测定培养基中前基质金属蛋白酶-3(ProMMP-3)、组织金属蛋白酶抑制剂-1(TIMP-1)和-2的浓度。

结果

通过免疫组织化学发现,IL-1β刺激后PG阴性细胞显著增加。TGF-β预处理几乎完全抑制了IL-1β引起的PG阴性细胞的增加。IL-1β刺激后,培养基中GAG和ProMMP-3的浓度均显著增加。有无IL-1β刺激时,培养基中TIMP-1和TIMP-2的浓度均无显著差异。800 kDa的HA显著减少了培养基中PG阴性细胞的数量和ProMMP-3的浓度,但对两种TIMP的浓度均无影响。

结论

由于这种藻酸盐珠中的三维软骨细胞培养接近体内条件,该方法可用于评估治疗关节疾病新药的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ffe/3614739/12a6d10b99b7/IJBS-6-103_F1.jpg

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