A reliable and convenient method to store ultrathin thawed cryosections prior to immunolabeling

被引:31
作者
Griffith, JM
Posthuma, G
机构
[1] Univ Utrecht, Med Ctr, Dept Cell Biol, NL-3584 CX Utrecht, Netherlands
[2] Univ Utrecht, Med Ctr, Inst Biomembranes, Utrecht, Netherlands
关键词
ultrathin cryosection; storage; immunogold labeling;
D O I
10.1177/002215540205000106
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ultracryotomy of fixed specimens in combination with immunogold labeling is widely used for ultrastructural localization of many interesting molecules. Since the introduction of this technique, vast improvements in techniques and machinery have been established and the entire process has been made easier and more accessible. Normally, sections are cut and labeled within 1 day to prevent possible loss or redistribution of soluble antigens within the sections. An increasing demand for more sections and multiple labeling protocols prompted us to investigate the extent to which ultrathin cryosections can be stored. This would render the time spent behind an ultracryomicrotome more efficient and would allow immunogold labeling at a later stage. We investigated whether gelatin plates, 2.3 M sucrose, or 1.0% methyl cellulose/1.2 M sucrose can be used to store thawed frozen sections for a longer period of time. Ultrathin sections of mildly fixed tissue and cultured cells were stored for up to 6 months before immunogold labeling. The preservation of the ultrastructure of stored sections was excellent and was similar to that of immediately processed sections. Importantly, prolonged storage did not affect the labeling intensity.
引用
收藏
页码:57 / 62
页数:6
相关论文
共 10 条
[1]  
[Anonymous], 1979, STEREOLOGICAL METHOD
[2]   THE PRODUCTION OF RECOMBINANT HLA-DR-BETA AND INVARIANT CHAIN POLYPEPTIDES BY CDNA EXPRESSION IN ESCHERICHIA-COLI [J].
KOCH, S ;
SCHULTZ, A ;
KOCH, N .
JOURNAL OF IMMUNOLOGICAL METHODS, 1987, 103 (02) :211-220
[3]   Improving structural integrity of cryosections for immunogold labeling [J].
Liou, W ;
Geuze, HJ ;
Slot, JW .
HISTOCHEMISTRY AND CELL BIOLOGY, 1996, 106 (01) :41-58
[4]   CRYOSUBSTITUTION DEHYDRATION OF ALDEHYDE-FIXED TISSUE - A FAVORABLE APPROACH TO QUANTITATIVE IMMUNOCYTOCHEMISTRY [J].
OPRINS, A ;
GEUZE, HJ ;
SLOT, JW .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1994, 42 (04) :497-503
[5]   USEFULNESS OF THE IMMUNOGOLD TECHNIQUE IN QUANTITATION OF A SOLUBLE-PROTEIN IN ULTRA-THIN SECTIONS [J].
POSTHUMA, G ;
SLOT, JW ;
GEUZE, HJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1987, 35 (04) :405-410
[6]   IMMUNO-LOCALIZATION OF THE INSULIN REGULATABLE GLUCOSE TRANSPORTER IN BROWN ADIPOSE-TISSUE OF THE RAT [J].
SLOT, JW ;
GEUZE, HJ ;
GIGENGACK, S ;
LIENHARD, GE ;
JAMES, DE .
JOURNAL OF CELL BIOLOGY, 1991, 113 (01) :123-135
[7]   COMPOSITION OF THE TRANSFER MEDIUM IS CRUCIAL FOR HIGH-RESOLUTION IMMUNOCYTOCHEMISTRY OF CRYOSECTIONED HUMAN NEUTROPHILS [J].
TAKIZAWA, T ;
ROBINSON, JM .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1994, 42 (08) :1157-1159
[8]   STUDY OF POSITIVE STAINING OF ULTRATHIN FROZEN SECTIONS [J].
TOKUYASU, KT .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1978, 63 (03) :287-307
[9]  
TOKUYASU KT, 1997, CELLS LAB MANUAL, V3
[10]   Maturation stages of mouse dendritic cells in growth factor-dependent long-term cultures [J].
Winzler, C ;
Rovere, P ;
Rescigno, M ;
Granucci, F ;
Penna, G ;
Adorini, L ;
Zimmermann, VS ;
Davoust, J ;
RicciardiCastagnoli, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (02) :317-328