PMID- 17959074 OWN - NLM STAT- MEDLINE DCOM- 20081023 LR - 20140226 IS - 0578-1426 (Print) IS - 0578-1426 (Linking) VI - 46 IP - 7 DP - 2007 Jul TI - [Expression of high mobility group box chromosomal protein 1 in peripheral blood of patients with rheumatoid arthritis]. PG - 547-50 AB - OBJECTIVE: To investigate the mRNA and protein expression of high mobility group box chromosomal protein 1 (HMGB1) in peripheral blood mononuclear cells (PBMCs) and serum. METHODS: Levels of HMGB1mRNA were detected with reverse transcription polymerase chain reaction (RT-PCR) in PBMC and levels of HMGB1 protein in PBMC and plasm were measured with Western blot in 38 patients with active rheumatoid arthritis (RA), 24 with inactive RA and 20 healthy controls. Ficoll density gradient centrifugation was used to separate PBMCs from peripheral blood. The correlation between the levels of HMGB1 in serum and the index of disease activity in RA was analyzed. RESULTS: There was no statistically significant difference of the mRNA expression of HMGB1 in PBMCs from active RA patients as compared with those from inactive RA group and healthy controls (F = 1.23, P > 0.05). The protein expression of HMGB1 was significantly lower in PBMCs from active RA patients (F = 70.91, P < 0.01), while the protein expression of HMGB1 was higher in plasma from active RA patients (P < 0.001) as compared with that from inactive RA patients and healthy controls. However, there was no statistically significant difference between inactive RA patients and healthy controls (P > 0.05). The level of HMGB1 protein in plasma of RA patients was correlated with erythrocyte sedimentation rate (ESR) (r(s) = 0.478, P < 0.001) and C- reactive protein (CRP) (r(s) = 0.574, P < 0.05). It was not correlated with age, the number of tender joints and swollen joints, radiographic scores and therapeutic effect. CONCLUSION: The protein expression of HMGB1 was significantly decreased in PBMCs from active RA patients, while it was increased in serum from active RA patients. HMGB1 plays a pivotal role in the pathogenesis of RA and may be a target of therapy as a novel cytokine. FAU - Zuo, Xiao-xia AU - Zuo XX AD - Department of Rheumatology and Clinical Immunology, Xiangya Hospital, Central South University, Changsha 410008, China. susanzuo@hotmail.com FAU - Zhou, Ya-ou AU - Zhou YO FAU - Gong, Yan-hui AU - Gong YH FAU - Wang, Yan-ping AU - Wang YP FAU - Tang, Dao-lin AU - Tang DL FAU - Xiao, Xian-zhong AU - Xiao XZ LA - chi PT - English Abstract PT - Journal Article PL - China TA - Zhonghua Nei Ke Za Zhi JT - Zhonghua nei ke za zhi JID - 16210490R RN - 0 (HMGB1 Protein) RN - 0 (RNA, Messenger) RN - 9007-41-4 (C-Reactive Protein) SB - IM MH - Adult MH - Arthritis, Rheumatoid/*blood/pathology MH - Blotting, Western MH - C-Reactive Protein/metabolism MH - Female MH - Gene Expression MH - HMGB1 Protein/*blood/genetics/metabolism MH - Humans MH - Leukocytes, Mononuclear/cytology/metabolism MH - Male MH - Middle Aged MH - RNA, Messenger/genetics/metabolism MH - Reverse Transcriptase Polymerase Chain Reaction EDAT- 2007/10/26 09:00 MHDA- 2008/10/24 09:00 CRDT- 2007/10/26 09:00 PHST- 2007/10/26 09:00 [pubmed] PHST- 2008/10/24 09:00 [medline] PHST- 2007/10/26 09:00 [entrez] PST - ppublish SO - Zhonghua Nei Ke Za Zhi. 2007 Jul;46(7):547-50.