Department of Geriatric Pharmacology and Therapeutics, Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8675, Japan.
J Cell Biochem. 2012 Mar;113(3):1054-60. doi: 10.1002/jcb.23436.
Histamine has been regarded as an inflammatory mediator of arthritic disorders. We have previously reported that the expression of histamine H(4) receptor (H(4)R) mRNA in synovial tissues was significantly higher in patients with osteoarthritis (OA) compared to those with rheumatoid arthritis. Chondrocyte hypertrophy and endochondral ossification are essential processes in pathologic disorders such as osteophyte formation during OA progression. In the present study, we examined the expression of H(4) R during differentiation into hypertrophic chondrocytes in the ATDC5 cells, a widely used in vitro model of chondrogenic differentiation. Quantitative reverse transcription polymerase chain reaction showed that the levels of histidine decarboxylase and H(4)R mRNA on ATDC5 cells were increased in a time-dependent manner during the culture period. By contrast, the expressions of H(1)R and H(2)R were not increased from day 7 onwards. The mRNA expression of the hypertrophic chondrocyte marker type X collagen (COL X) was increased markedly from 14 to 21. Immunocytochemical analysis indicated that H(4)R staining was strongly immunoreactive on the plasma membrane of ATDC5 cells. Flow cytometry showed increased expression of H(4)R and COL X protein in ATDC5 chondrocytes. Furthermore, the majority of the COL X-positive cells expressed H(4) R throughout the culture period. In summary, we showed for the first time that H(4)R is expressed in ATDC5 chondrocytes. Moreover, we found that most hypertrophic chondrocytes express H(4)R, suggesting that this receptor might be associated with the differentiation of chondrocytes into hypertrophic cells, which are abnormally observed in joint lesions in OA.
组胺一直被认为是关节炎疾病的炎症介质。我们之前曾报道过,与类风湿关节炎患者相比,骨关节炎(OA)患者滑膜组织中组胺 H(4)受体(H(4)R)mRNA 的表达明显更高。软骨细胞肥大和软骨内骨化是病理性疾病(如 OA 进展过程中骨赘形成)的重要过程。在本研究中,我们研究了 H(4)R 在 ATDC5 细胞分化为肥大软骨细胞过程中的表达,ATDC5 细胞是软骨分化的常用体外模型。定量逆转录聚合酶链反应显示,在培养期间,ATDC5 细胞中的组氨酸脱羧酶和 H(4)R mRNA 的水平呈时间依赖性增加。相比之下,从第 7 天开始,H(1)R 和 H(2)R 的表达没有增加。肥大软骨细胞标志物 X 型胶原(COL X)的 mRNA 表达从第 14 天到第 21 天明显增加。免疫细胞化学分析表明,H(4)R 染色在 ATDC5 细胞的质膜上强烈免疫反应性。流式细胞术显示 ATDC5 软骨细胞中 H(4)R 和 COL X 蛋白表达增加。此外,在整个培养过程中,大多数 COL X 阳性细胞表达 H(4)R。总之,我们首次表明 H(4)R 在 ATDC5 软骨细胞中表达。此外,我们发现大多数肥大软骨细胞表达 H(4)R,这表明该受体可能与软骨细胞向肥大细胞分化有关,这在 OA 关节病变中是异常的。