The 1D4 Antibody Labels Outer Segments of Long Double Cone But Not Rod Photoreceptors in Zebrafish

被引:38
作者
Yin, Jun [1 ,2 ,4 ]
Brocher, Jan [1 ,2 ,5 ]
Linder, Bastian [3 ]
Hirmer, Anja [3 ]
Sundaramurthi, Husvinee [1 ,2 ]
Fischer, Utz [3 ]
Winkler, Christoph [1 ,2 ]
机构
[1] Natl Univ Singapore, Dept Biol Sci, Singapore 117543, Singapore
[2] Natl Univ Singapore, Ctr Bioimaging Sci CBIS, Singapore 117543, Singapore
[3] Univ Wurzburg, Bioctr, Dept Biochem, Wurzburg, Germany
[4] Univ Calif Davis, Det Biochem & Mol Med, Davis, CA 95616 USA
[5] BioVoxxel, Mutterstadt, Germany
关键词
VERTEBRATE VISUAL PIGMENTS; RETINITIS-PIGMENTOSA; MONOCLONAL-ANTIBODIES; TRANSGENIC ZEBRAFISH; RETINAL DEGENERATION; OPSIN GENES; RHODOPSIN; EVOLUTION; MUTATION; MODEL;
D O I
10.1167/iovs.12-9511
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. In experimental eye research, zebrafish has become a powerful model for human retina disorders. The purpose of the present study is the characterization of antibodies commonly employed in zebrafish models for rod photoreceptor degeneration. METHODS. The 1D4 monoclonal antibody, developed against bovine rhodopsin, has been widely used in studies addressing structural and functional features of rhodopsin and was reported as an informative marker to stain rod outer segments in both mice and zebrafish. We have used transgenic reporter lines and histologic analysis to determine the photoreceptor types identified by 1D4 and other antibodies in zebrafish. RESULTS. We demonstrate that 1D4, in contrast to what has been reported previously, does not recognize rod outer segments in zebrafish, but instead labels long double cone outer segments consistent with sequence conservation of the respective epitope. As an alternative marker for zebrafish rods, we characterized the monoclonal antibody zpr-3, which was found to stain outer segments of both rods, as well as double cones. CONCLUSIONS. Our findings highlight the importance to confirm specificity of antibodies in cross-species experiments for correct interpretation of experimental data. Our findings clarify conflicting published information arising from studies using 1D4 and zpr-3 antibodies in zebrafish. (Invest Ophthalmol Vis Sci. 2012;53:4943-4951) DOI:10.1167/iovs.12-9511
引用
收藏
页码:4943 / 4951
页数:9
相关论文
共 35 条
[1]  
al-Jandal N, 1999, HUM MUTAT, V13, P75, DOI 10.1002/(SICI)1098-1004(1999)13:1<75::AID-HUMU9>3.0.CO
[2]  
2-4
[3]   Toward a Better Understanding of Human Eye Disease: Insights From the Zebrafish, Danio rerio [J].
Bibliowicz, Jonathan ;
Tittle, Rachel K. ;
Gross, Jeffrey M. .
ANIMAL MODELS OF HUMAN DISEASE, 2011, 100 :287-330
[4]   Evolution of vertebrate visual pigments [J].
Bowmaker, James K. .
VISION RESEARCH, 2008, 48 (20) :2022-2041
[5]   The spectrum of human rhodopsin disease mutations through the lens of interspecific variation [J].
Briscoe, AD ;
Gaur, C ;
Kumar, S .
GENE, 2004, 332 :107-118
[6]   Genetics of photoreceptor degeneration and regeneration in zebrafish [J].
Brockerhoff, Susan E. ;
Fadool, James M. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2011, 68 (04) :651-659
[7]  
Chinen A, 2003, GENETICS, V163, P663
[8]   The zebrafish as a tool for understanding the biology of visual disorders [J].
Goldsmith, P ;
Harris, WA .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2003, 14 (01) :11-18
[9]   Visualization of rod photoreceptor development using GFP-transgenic zebrafish [J].
Hamaoka, T ;
Takechi, M ;
Chinen, A ;
Nishiwaki, Y ;
Kawamura, S .
GENESIS, 2002, 34 (03) :215-220
[10]   Isolation of a zebrafish rod opsin promoter to generate a transgenic zebrafish line expressing enhanced green fluorescent protein in rod photoreceptors [J].
Kennedy, BN ;
Vihtelic, TS ;
Checkley, L ;
Vaughan, KT ;
Hyde, DR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (17) :14037-14043