Characterization of Antibodies to Products of Proinsulin Processing Using Immunofluorescence Staining of Pancreas in Multiple Species

被引:29
作者
Asadi, Ali [1 ]
Bruin, Jennifer E. [1 ]
Kieffer, Timothy J. [1 ,2 ]
机构
[1] Univ British Columbia, Inst Life Sci, Dept Cellular & Physiol Sci, Lab Mol & Cellular Med, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Dept Surg, Vancouver, BC V6T 1Z3, Canada
关键词
beta cells; diabetes; immunofluorescence staining; islets; proinsulin processing; DEPENDENT DIABETES-MELLITUS; DISPROPORTIONATELY ELEVATED PROINSULIN; INDUCED INSULIN-SECRETION; BETA-CELLS; C-PEPTIDE; PROHORMONE CONVERTASE-1/3; RAT; HETEROGENEITY; BIOSYNTHESIS; EXPRESSION;
D O I
10.1369/0022155415576541
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The efficient processing of proinsulin into mature insulin and C-peptide is often compromised under conditions of beta cell stress, including diabetes. Impaired proinsulin processing has been challenging to examine by immunofluorescence staining in pancreas tissue because the characterization of antibodies specific for proinsulin, proinsulin intermediates, processed insulin and C-peptide has been limited. This study aimed to identify and characterize antibodies that can be used to detect products of proinsulin processing by immunofluorescence staining in pancreata from different species (mice, rats, dog, pig and human). We took advantage of several knockout mouse lines that lack either an enzyme involved in proinsulin processing or an insulin gene. Briefly, we report antibodies that are specific for several proinsulin processing products, including: a) insulin or proinsulin that has been appropriately processed at the B-C junction; b) proinsulin with a non-processed B-C junction; c) proinsulin with a non-processed A-C junction; d) rodent-specific C-peptide 1; e) rodent-specific C-peptide 2; and f) human-specific C-peptide or proinsulin. In addition, we also describe two pan-insulin' antibodies that react with all forms of insulin and proinsulin intermediates, regardless of the species. These antibodies are valuable tools for studying proinsulin processing by immunofluorescence staining and distinguishing between proinsulin products in different species.
引用
收藏
页码:646 / 662
页数:17
相关论文
共 29 条
[21]   The proinsulin C-peptide - A multirole model [J].
Steiner, DF .
EXPERIMENTAL DIABESITY RESEARCH, 2004, 5 (01) :7-14
[22]   Maturation of Adult β-Cells Revealed Using a Pdx1/Insulin Dual-Reporter Lentivirus [J].
Szabat, Marta ;
Luciani, Dan S. ;
Piret, James M. ;
Johnson, James D. .
ENDOCRINOLOGY, 2009, 150 (04) :1627-1635
[23]   Proinsulin levels and the proinsulin:C-peptide ratio complement autoantibody measurement for predicting type 1 diabetes [J].
Truyen, I ;
Pauw, P ;
Jorgensen, PN ;
Van Schravendijk, C ;
Ubani, O ;
Decochez, K ;
Vandemeulebroucke, E ;
Weets, I ;
Mao, R ;
Pipeleers, DG ;
Gorus, FK .
DIABETOLOGIA, 2005, 48 (11) :2322-2329
[24]  
VANSCHRAVENDIJK CFH, 1992, J BIOL CHEM, V267, P21344
[25]   DISPROPORTIONATE ELEVATION OF IMMUNOREACTIVE PROINSULIN IN TYPE-2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS AND IN EXPERIMENTAL INSULIN RESISTANCE [J].
WARD, WK ;
LACAVA, EC ;
PAQUETTE, TL ;
BEARD, JC ;
WALLUM, BJ ;
PORTE, D .
DIABETOLOGIA, 1987, 30 (09) :698-702
[26]   Beta cell-specific Znt8 deletion in mice causes marked defects in insulin processing, crystallisation and secretion [J].
Wijesekara, N. ;
Dai, F. F. ;
Hardy, A. B. ;
Giglou, P. R. ;
Bhattacharjee, A. ;
Koshkin, V. ;
Chimienti, F. ;
Gaisano, H. Y. ;
Rutter, G. A. ;
Wheeler, M. B. .
DIABETOLOGIA, 2010, 53 (08) :1656-1668
[27]   SERUM PROINSULIN LEVELS AT FASTING AND AFTER ORAL GLUCOSE-LOAD IN PATIENTS WITH TYPE-2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS [J].
YOSHIOKA, N ;
KUZUYA, T ;
MATSUDA, A ;
TANIGUCHI, M ;
IWAMOTO, Y .
DIABETOLOGIA, 1988, 31 (06) :355-360
[28]   Severe block in processing of proinsulin to insulin accompanied by elevation of des-64,65 proinsulin intermediates in islets of mice lacking prohormone convertase-1/3 [J].
Zhu, XR ;
Orci, L ;
Carroll, R ;
Norrbom, C ;
Ravazzola, M ;
Steiner, DF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10299-10304
[29]   Disruption of PC1/3 expression in mice causes dwarfism and multiple neuroendocrine peptide processing defects [J].
Zhu, XR ;
Zhou, A ;
Dey, A ;
Norrbom, C ;
Carroll, R ;
Zhang, CL ;
Laurent, V ;
Lindberg, I ;
Ugleholdt, R ;
Holst, JJ ;
Steiner, DF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10293-10298