Nakatsuka K, Kurita K, Hayakawa Taro, Nakashima Katsuhito, Yamashita Kyoko, Hoshino Takeshi, Miyazaki Kyosuke
Department of Oral and Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin Unuverity, Japan;
Int J Biomed Sci. 2010 Jun;6(2):103-10.
A 3-dimensional alginate bead culturing method using rabbit articular chondrocytes was studied for the screening of the effectiveness of drugs for articular diseases.
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.
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.
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.
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。
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。
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。
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。