Serum based fluorescent assay for evaluating dipeptidyl peptidase I activity in collagen induced arthritis rat model

被引:14
作者
Liu, Xiaoqian [1 ]
Wang, Jingjing [1 ]
Chu, Yi [1 ]
Zhou, Xiaoying [1 ]
机构
[1] Changzhou Univ, Sch Pharmaceut Engn & Life Sci, Changzhou 213164, Jiangsu, Peoples R China
关键词
DPPI activity; Rheumatoid arthritis; Serum based assay; Fluorescent probe; CATHEPSIN-C; EXPRESSION; ACTIVATION; LOCALIZATION; PURIFICATION; INHIBITION; PROBE; MICE;
D O I
10.1016/j.mcp.2016.10.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dipeptidyl peptidase I (DPPI) is a lysosomal cysteine protease and derived from immune granule cells. It has been suggested playing an important role in the development of rheumatoid arthritis. In this study, a coumarin based fluorescent probe (GF-AFC) was designed and synthesized to evaluate DPPI activity in serum or tissue homogenates of collagen-induced arthritis (CIA) rats, an inflammatory arthropathy model. It was revealed that the fluorescent intensity was significantly increased in a very short time after specific substrate GF-AFC reacted with the DPPI. The fluorophore (AFC) was released to shine after the cleavage reaction which was examined by F-19 NMR spectroscopy. It has been shown that DPPI hydrolyzed the GF-AFC in a robust, linear, and time dependent manner at a significant high rate. A serum-based DPPI activity assay was validated by spiking and gradient dilution methods, there were no interferences or auto-fluorescence observed. The Coefficient of Variance calculated for serum-based DPPI activity assays indicates the good reproducibility. The good correlation has been seen between serum DPPI levels and the severity of arthritis during RA development in CIA rats. Our study has demonstrated a new serum based diagnostic assay for detecting DPPI activity using coumarin conjugated fluorescent (GF-AFC) as a substrate. The successful implementation of the case would provide beneficial experience in rheumatoid arthritis research.(C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5 / 12
页数:8
相关论文
共 33 条
[1]   Clinical and histopathological characterization of a large animal (ovine) model of collagen-induced arthritis [J].
Abdalmula, A. ;
Washington, E. A. ;
House, J. V. ;
Dooley, L. M. ;
Blacklaws, B. A. ;
Ghosh, P. ;
Bailey, S. R. ;
Kimpton, W. G. .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2014, 159 (1-2) :83-90
[2]  
Adkison AM, 2002, J CLIN INVEST, V109, P363, DOI 10.1172/JCI200213462
[3]  
Al-Qubaeissy KY, 2013, MUSCULOSKELETAL CARE, V11, P3
[4]   Statistical media optimization and alkaline protease production from Bacillus mojavensis in a bioreactor [J].
Beg, QK ;
Sahai, V ;
Gupta, R .
PROCESS BIOCHEMISTRY, 2003, 39 (02) :203-209
[5]   Lysosomal degradation of cholecystokinin-(29-33)-amide in mouse brain is dependent on tripeptidyl peptidase-I: implications for the degradation and storage of peptides in classical late-infantile neuronal ceroid lipofuscinosis [J].
Bernardini, F ;
Warburton, MJ .
BIOCHEMICAL JOURNAL, 2002, 366 :521-529
[6]   SOME 7-SUBSTITUTED 4-(TRIFLUOROMETHYL)COUMARINS [J].
BISSELL, ER ;
LARSON, DK ;
CROUDACE, MC .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1981, 26 (03) :348-350
[7]   Novel semicarbazide-derived inhibitors of human dipeptidyl peptidase I (hDPPI) [J].
Bondebjerg, J ;
Fuglsang, H ;
Valeur, KR ;
Kaznelson, DW ;
Hansen, JA ;
Pedersen, RO ;
Krogh, BO ;
Jensen, BS ;
Lauritzen, C ;
Petersen, G ;
Pedersen, J ;
Nærum, L .
BIOORGANIC & MEDICINAL CHEMISTRY, 2005, 13 (14) :4408-4424
[8]   Shuangtengbitong tincture treatment of collagen-induced arthritis via downregulation of the expression of IL-6, IL-8, TNF-α and NF-κB [J].
Chu, Kedan ;
Zheng, Haiyin ;
Li, Huang ;
Zhang, Yuqin ;
Zhang, Xun ;
Xu, We ;
Chen, Lidian .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2013, 5 (02) :423-428
[9]   OLIGOMERIC STRUCTURE AND SUBSTRATE-INDUCED INHIBITION OF HUMAN CATHEPSIN-C [J].
DOLENC, I ;
TURK, B ;
PUNGERCIC, G ;
RITONJA, A ;
TURK, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (37) :21626-21631
[10]   THE ACTIVITY OF DIPEPTIDYL PEPTIDASE-II AND DIPEPTIDYL PEPTIDASE-IV IN MICE IMMUNIZED WITH TYPE-II COLLAGEN [J].
FUJITA, K ;
HAGIHARA, M ;
NAGATSU, T ;
IWATA, H ;
MIURA, T .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1992, 48 (03) :227-234