期刊论文详细信息
BMC Musculoskeletal Disorders
Increased proteasome activator 28 gamma (PA28γ) levels are unspecific but correlate with disease activity in rheumatoid arthritis
Ralf Stohwasser2  Eugen Feist1  Dagmar Kühnhardt4  Stefan Rödiger2  Anja Moncsek3  Melanie Gruner1 
[1]Department of Rheumatology and Clinical Immunology and Autoinflammatory Reference Centre at Charité, Charité-Universitätsmedizin Berlin, Charitéplatz 1, D-10117 Berlin, Germany
[2]Faculty of Natural Sciences, Brandenburg Technical University Cottbus - Senftenberg, Großenhainer Str. 57, D-01968 Senftenberg, Germany
[3]Department of Biochemistry, Charité-Universitätsmedizin Berlin, Charitéplatz 1, D-10117 Berlin, Germany
[4]Department of Hematology and Oncology, Charité-Universitätsmedizin Berlin, Charitéplatz 1, D-10117 Berlin, Germany
关键词: Cancer;    Abatacept;    Rheumatoid arthritis;    Autoimmune disorders;    Microbeads;    Sandwich ELISA;    20S proteasome;    Proteasome activator PA28γ;   
Others  :  1091040
DOI  :  10.1186/1471-2474-15-414
 received in 2014-09-08, accepted in 2014-11-28,  发布年份 2014
PDF
【 摘 要 】

Background

PA28γ (also known as Ki, REG gamma, PMSE3), a member of the ubiquitin-and ATP-independent proteasome activator family 11S, has been proved to show proteasome-dependent and -independent effects on several proteins including tumor suppressor p53, cyclin-dependent kinase inhibitor p21 and steroid receptor co-activator 3 (SCR-3). Interestingly, PA28γ is overexpressed in pathological tissue of various cancers affecting e. g. breast, bowl and thyroids. Furthermore, anti-PA28γ autoantibodies have been linked to several autoimmune disorders. The aim of this study was to develop and evaluate a novel and sensitive PA28γ sandwich ELISA for the quantification of PA28γ serum levels in patients with cancer and autoimmune diseases for diagnostic and prognostic purposes.

Methods

PA28γ-specific polyclonal antibodies and recombinant His-tagged PA28γ were purified and used to develop a sandwich ELISA for the detection of circulating PA28γ. With this new assay, PA28γ serum levels of patients with various cancers, rheumatoid arthritis (RA), Sjögren’s syndrome (SS), adult-onset Still’s disease (AOSD) and different connective-tissue diseases (CTD) were compared with healthy control subjects. Anti-PA28γ autoantibodies were additionally confirmed using a newly developed microbead assay.

Results

The developed PA28γ sandwich ELISA showed a high specificity with a detection limit of 3 ng/ml. A significant up-regulation of circulating PA28γ was detected in the sera of patients with cancer, RA, SS and CTD. A significant correlation was observed dependent on age as well as anti-PA28γ autoantibody levels with circulating PA28γ protein levels. Furthermore, PA28γ serum levels showed a correlation with disease activity in patients with RA under treatment with the T-cell directed biological compound abatacept according to disease activity score 28 (DAS28) and erythrocyte sedimentation rate (ESR).

Conclusion

The application of PA28γ as a novel biomarker for diagnostic purposes of a specific disease is limited, since elevated levels were observed in different disorders. However, the correlation with disease activity in patients with RA suggests a prognostic value, which needs to be addressed by further studies. Therefore our results show that PA28γ is a useful marker which should be included in studies related to novel treatments, e.g. abatacept.

【 授权许可】

   
2014 Gruner et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150128165104428.pdf 738KB PDF download
Figure 3. 78KB Image download
Figure 2. 41KB Image download
Figure 1. 66KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

【 参考文献 】
  • [1]Ciechanover A: The ubiquitin-proteasome pathway: on protein death and cell life. EMBO J 1998, 17:7151-7160.
  • [2]Stadtmueller BM, Hill CP: Proteasome activators. Mol Cell 2011, 41:8-19.
  • [3]Tanaka K, Mizushima T, Saeki Y: The proteasome: molecular machinery and pathophysiological roles. Biol Chem 2012, 393:217-234.
  • [4]Finley D: Recognition and processing of ubiquitin-protein conjugates by the proteasome. Annu Rev Biochem 2009, 78:477-513.
  • [5]Sijts EJAM, Kloetzel PM: The role of the proteasome in the generation of MHC class I ligands and immune responses. Cell Mol Life Sci 2011, 68:1491-1502.
  • [6]Dahlmann B: Role of proteasomes in disease. BMC Biochem 2007, 8(Suppl 1):S3. BioMed Central Full Text
  • [7]Krause S, Kuckelkorn U, Dörner T, Burmester G-R, Feist E, Kloetzel P-M: Immunoproteasome subunit LMP2 expression is deregulated in Sjogren’s syndrome but not in other autoimmune disorders. Ann Rheum Dis 2006, 65:1021-1027.
  • [8]Martinez-Gamboa L, Lesemann K, Kuckelkorn U, Scheffler S, Ghannam K, Hahne M, Gaber-Elsner T, Egerer K, Naumann L, Buttgereit F, Dörner T, Kloetzel PM, Burmester GR, Faustman DL, Feist E: Gene expression of catalytic proteasome subunits and resistance toward proteasome inhibition of B lymphocytes from patients with primary sjogren syndrome. J Rheumatol 2013, 40:663-673.
  • [9]Egerer K, Kuckelkorn U, Rudolph PE, Rückert JC, Dörner T, Burmester G-R, Kloetzel P-M, Feist E: Circulating proteasomes are markers of cell damage and immunologic activity in autoimmune diseases. J Rheumatol 2002, 29:2045-2052.
  • [10]Jakob C, Egerer K, Liebisch P, Türkmen S, Zavrski I, Kuckelkorn U, Heider U, Kaiser M, Fleissner C, Sterz J, Kleeberg L, Feist E, Burmester G-R, Kloetzel P-M, Sezer O: Circulating proteasome levels are an independent prognostic factor for survival in multiple myeloma. Blood 2007, 109:2100-2105.
  • [11]Mao I, Liu J, Li X, Luo H: REGgamma, a proteasome activator and beyond? Cell Mol Life Sci 2008, 65:3971-3980.
  • [12]Li X, Lonard DM, Jung SY, Malovannaya A, Feng Q, Qin J, Tsai SY, Tsai M-J, O’Malley BW: The SRC-3/AIB1 coactivator is degraded in a ubiquitin- and ATP-independent manner by the REGgamma proteasome. Cell 2006, 124:381-392.
  • [13]Chen X, Barton LF, Chi Y, Clurman BE, Roberts JM: Ubiquitin-independent degradation of cell-cycle inhibitors by the REGgamma proteasome. Mol Cell 2007, 26:843-852.
  • [14]Li X, Amazit L, Long W, Lonard DM, Monaco JJ, O’Malley BW: Ubiquitin- and ATP-independent proteolytic turnover of p21 by the REGgamma-proteasome pathway. Mol Cell 2007, 26:831-842.
  • [15]Suzuki R, Moriishi K, Fukuda K, Shirakura M, Ishii K, Shoji I, Wakita T, Miyamura T, Matsuura Y, Suzuki T: Proteasomal turnover of hepatitis C virus core protein is regulated by two distinct mechanisms: a ubiquitin-dependent mechanism and a ubiquitin-independent but PA28gamma-dependent mechanism. J Virol 2009, 83:2389-2392.
  • [16]Nie J, Wu M, Wang J, Xing G, He F, Zhang L: REGgamma proteasome mediates degradation of the ubiquitin ligase Smurf1. FEBS Lett 2010, 584:3021-3027.
  • [17]Kanai K, Aramata S, Katakami S, Yasuda K, Kataoka K: Proteasome activator PA28γ stimulates degradation of GSK3-phosphorylated insulin transcription activator MAFA. J Mol Endocrinol 2011, 47:119-127.
  • [18]Zannini L, Lecis D, Buscemi G, Carlessi L, Gasparini P, Fontanella E, Lisanti S, Barton L, Delia D: REGgamma proteasome activator is involved in the maintenance of chromosomal stability. Cell Cycle Georget Tex 2008, 7:504-512.
  • [19]Baldin V, Militello M, Thomas Y, Doucet C, Fic W, Boireau S, Jariel-Encontre I, Piechaczyk M, Bertrand E, Tazi J, Coux O: A novel role for PA28gamma-proteasome in nuclear speckle organization and SR protein trafficking. Mol Biol Cell 2008, 19:1706-1716.
  • [20]Anupam R, Datta A, Kesic M, Green-Church K, Shkriabai N, Kvaratskhelia M, Lairmore MD: Human T-lymphotropic virus type 1 p30 interacts with REGgamma and modulates ATM (ataxia telangiectasia mutated) to promote cell survival. J Biol Chem 2011, 286:7661-7668.
  • [21]Ko NL, Taylor JM, Bellon M, Bai XT, Shevtsov SP, Dundr M, Nicot C: PA28γ is a novel corepressor of HTLV-1 replication and controls viral latency. Blood 2013, 121:791-800.
  • [22]Zhang Z, Zhang R: Proteasome activator PA28 gamma regulates p53 by enhancing its MDM2-mediated degradation. EMBO J 2008, 27:852-864.
  • [23]Liu J, Yu G, Zhao Y, Zhao D, Wang Y, Wang L, Liu J, Li L, Zeng Y, Dang Y, Wang C, Gao G, Long W, Lonard DM, Qiao S, Tsai M-J, Zhang B, Luo H, Li X: REGgamma modulates p53 activity by regulating its cellular localization. J Cell Sci 2010, 123(Pt 23):4076-4084.
  • [24]Roessler M, Rollinger W, Mantovani-Endl L, Hagmann M-L, Palme S, Berndt P, Engel AM, Pfeffer M, Karl J, Bodenmüller H, Rüschoff J, Henkel T, Rohr G, Rossol S, Rösch W, Langen H, Zolg W, Tacke M: Identification of PSME3 as a novel serum tumor marker for colorectal cancer by combining two-dimensional polyacrylamide gel electrophoresis with a strictly mass spectrometry-based approach for data analysis. Mol Cell Proteomics 2006, 5:2092-2101.
  • [25]Chen D, Yang X, Huang L, Chi P: The expression and clinical significance of PA28 γ in colorectal cancer. J Investig Med Off Publ Am Fed Clin Res 2013, 61:1192-1196.
  • [26]Wang X, Tu S, Tan J, Tian T, Ran L, Rodier J-F, Ren G: REG gamma: a potential marker in breast cancer and effect on cell cycle and proliferation of breast cancer cell. Med Oncol Northwood Lond Engl 2011, 28:31-41.
  • [27]Li L-P, Cheng W-B, Li H, Li W, Yang H, Wen D-H, Tang Y-D: Expression of proteasome activator REGγ in human laryngeal carcinoma and associations with tumor suppressor proteins. Asian Pac J Cancer Prev 2012, 13:2699-2703.
  • [28]He J, Cui L, Zeng Y, Wang G, Zhou P, Yang Y, Ji L, Zhao Y, Chen J, Wang Z, Shi T, Zhang P, Chen R, Li X: REGγ is associated with multiple oncogenic pathways in human cancers. BMC Cancer 2012, 12:75. BioMed Central Full Text
  • [29]Kondo M, Moriishi K, Wada H, Noda T, Marubashi S, Wakasa K, Matsuura Y, Doki Y, Mori M, Nagano H: Upregulation of nuclear PA28γ expression in cirrhosis and hepatocellular carcinoma. Exp Ther Med 2012, 3:379-385.
  • [30]Okamura T, Taniguchi S-I, Ohkura T, Yoshida A, Shimizu H, Sakai M, Maeta H, Fukui H, Ueta Y, Hisatome I, Shigemasa C: Abnormally high expression of proteasome activator-gamma in thyroid neoplasm. J Clin Endocrinol Metab 2003, 88:1374-1383.
  • [31]Zhang M, Gan L, Ren GS: REGγ is a strong candidate for the regulation of cell cycle, proliferation and the invasion by poorly differentiated thyroid carcinoma cells. Braz J Med Biol Res Rev Bras Pesqui Médicas E Biológicas Soc Bras Biofísica Al 2012, 45:459-465.
  • [32]Tojo T, Kaburaki J, Hayakawa M, Okamoto T, Tomii M, Homma M: Precipitating antibody to a soluble nuclear antigen “Ki” with specificity for systemic lupus erythematosus. Ryūmachi Rheum 1981, 21(Suppl):129-140.
  • [33]Yamanaka K, Takasaki Y, Nishida Y, Shimada K, Shibata M, Hashimoto H: Detection and quantification of anti-Ki antibodies by enzyme-linked immunosorbent assay using recombinant Ki antigen. Arthritis Rheum 1992, 35:667-671.
  • [34]Cavazzana I, Franceschini F, Vassalini C, Danieli E, Quinzanini M, Airò P, Cattaneo R: Clinical and serological features of 35 patients with anti-Ki autoantibodies. Lupus 2005, 14:837-841.
  • [35]Ahmed H: Principles and Reactions of Protein Extraction, Purification, and Characterization. Boca Raton: CRC Press; 2004.
  • [36]Rödiger S, Ruhland M, Schmidt C, Schröder C, Grossmann K, Böhm A, Nitschke J, Berger I, Schimke I, Schierack P: Fluorescence dye adsorption assay to quantify carboxyl groups on the surface of poly(methyl methacrylate) microbeads. Anal Chem 2011, 83:3379-3385.
  • [37]Rödiger S, Schierack P, Böhm A, Nitschke J, Berger I, Frömmel U, Schmidt C, Ruhland M, Schimke I, Roggenbuck D, Lehmann W, Schröder C: A highly versatile microscope imaging technology platform for the multiplex real-time detection of biomolecules and autoimmune antibodies. Adv Biochem Eng Biotechnol 2012, 133:35-74.
  • [38]Rödiger S, Friedrichsmeier T, Kapat P, Michalke M: RKWard: a comprehensive graphical user interface and integrated development environment for statistical analysis with R. J Stat Softw 2012, 49:1-34.
  • [39]Kohda K, Ishibashi T, Shimbara N, Tanaka K, Matsuda Y, Kasahara M: Characterization of the mouse PA28 activator complex gene family: complete organizations of the three member genes and a physical map of the approximately 150-kb region containing the alpha- and beta-subunit genes. J Immunol Baltim Md 1950 1998, 160:4923-4935.
  • [40]Li L, Zhao D, Wei H, Yao L, Dang Y, Amjad A, Xu J, Liu J, Guo L, Li D, Li Z, Zuo D, Zhang Y, Liu J, Huang S, Jia C, Wang L, Wang Y, Xie Y, Luo J, Zhang B, Luo H, Donehower LA, Moses RE, Xiao J, O’Malley BW, Li X: REGγ deficiency promotes premature aging via the casein kinase 1 pathway. Proc Natl Acad Sci 2013, 110:11005-10.
  • [41]Matsushita M, Matsudaira R, Ikeda K, Nawata M, Tamura N, Takasaki Y: Anti-proteasome activator 28alpha is a novel anti-cytoplasmic antibody in patients with systemic lupus erythematosus and Sjögren’s syndrome. Mod Rheumatol Jpn Rheum Assoc 2009, 19:622-628.
  • [42]Feist E, Kuckelkorn U, Dörner T, Dönitz H, Scheffler S, Hiepe F, Kloetzel PM, Burmester GR: Autoantibodies in primary Sjögren’s syndrome are directed against proteasomal subunits of the alpha and beta type. Arthritis Rheum 1999, 42:697-702.
  • [43]Henry L, Lavabre-Bertrand T, Vercambre L, Ramos J, Carillo S, Guiraud I, Pouderoux P, Bismuth M, Valats J-C, Demattei C, Duny Y, Chaze I, Funakoshi N, Bureau JP, Daurès J-P, Blanc P: Plasma proteasome level is a reliable early marker of malignant transformation of liver cirrhosis. Gut 2009, 58:833-838.
  文献评价指标  
  下载次数:20次 浏览次数:13次