Chemical Pretreatment of Growth Plate Cartilage Increases Immunofluorescence Sensitivity

被引:13
作者
Ahrens, Molly J. [1 ]
Dudley, Andrew T. [1 ]
机构
[1] Northwestern Univ, Dept Mol Biosci, Evanston, IL 60208 USA
基金
美国国家卫生研究院;
关键词
immunofluorescence; antibody; cartilage; antigen retrieval; autofluorescence; tissue pretreatment; NUCLEAR-PROTEIN; FIXED TISSUE; CHICK-EMBRYO; IX COLLAGEN; CYCLIN D1; DIFFERENTIATION; LOCALIZATION; CHONDROCYTES; CYTOSKELETON; EXPRESSION;
D O I
10.1369/0022155411400869
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Immunofluorescence detection of proteins in growth plate cartilage is often unsuccessful because of innate autofluorescence, fixative-induced fluorescence, and dense cartilage matrix, which can inhibit antibody penetration. To overcome these limitations, the authors have tested various chemical pretreatments, including the autofluorescence quencher sodium borohydride, the antigen retrieval method of boiling sodium citrate, sugar-degrading enzymes (hyaluronidase, heparinase, and chondroitinase), and the proteolytic enzyme protease XXIV. Here the authors show that, in most cases, background fluorescence in cartilage is the primary obstacle to high-quality imaging. Blocking intrinsic fluorescence of the specimen in combination with specific pretreatments allows visualization using antibodies that previously did not generate a robust signal in the growth plate. Each antibody requires a specific combination of chemical pretreatments that must be empirically determined to achieve optimal staining levels. This manuscript contains online supplemental material at http://www.jhc.org. Please visit this article online to view these materials. (J Histochem Cytochem 59:408-418, 2011)
引用
收藏
页码:408 / 418
页数:11
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