New strategies for embedding, orientation and sectioning of small brain specimens enable direct correlation to MR-images, brain atlases, or use of unbiased stereology

被引:38
作者
Bjarkam, CR [1 ]
Pedersen, M
Sorensen, JC
机构
[1] Aarhus Univ, Inst Anat, Dept Neurobiol, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, MR Res Ctr, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ Hosp, Dept Neurosurg, DK-8000 Aarhus C, Denmark
关键词
brain slicer; embedding medium; HistOmer; HistOtech vario slicer; tissue preparation;
D O I
10.1016/S0165-0270(01)00383-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We present a newly developed brain slicing machine and technique for tissue embedding, which enable orientation of fresh or fixed brain tissue from small laboratory animals, in any given position, and subsequent tissue sectioning into slabs with an optional thickness between 0.5 and 20 mm. The oriented tissue slabs may be analysed directly, or processed further on a cryostat or vibratome, into thin stainable histological sections, and aligned to MR-images or brain atlases, depending on the reference used for the initial orientation. Additionally, we describe a new embedding medium (HistOmer) which is an alginate cold polymer ready for instant use after mixing with water. HistOmer allows accurate positioning of the tissue during embedding, and at the same time supports and protects the embedded tissue during sectioning. HistOmer is, therefore, described comprehensively and compared with other commonly used embedding media. This novel slicing technique may also, as illustrated, be used to perform isotropic random orientation of the embedded tissue, before sectioning into tissue slabs of the same thickness. The technique thereby fulfills the requirements for optimal tissue sampling and preparation needed for an unbiased stereologic analysis. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:153 / 159
页数:7
相关论文
共 21 条
[1]   A BRAIN-SLICING APPARATUS FOR TISSUE RESPIRATION STUDIES [J].
ADDANKI, S ;
SOTOS, JF ;
REARICK, PD .
ANALYTICAL BIOCHEMISTRY, 1965, 13 (03) :458-&
[2]   A METHOD FOR DEFINED SECTIONING OF FRESH YOUNG BRAINS AND COLLECTION OF SMALL REGIONS FOR CELL AND TISSUE-CULTURE [J].
BUSE, E ;
MATTHAEI, H .
JOURNAL OF NEUROSCIENCE METHODS, 1983, 7 (04) :377-387
[3]  
Franklin K B J, 2008, MOUSE BRAIN STEREOTA
[4]   A RAPID METHOD FOR THE REGIONAL DISSECTION OF THE RAT-BRAIN [J].
HEFFNER, TG ;
HARTMAN, JA ;
SEIDEN, LS .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1980, 13 (03) :453-456
[5]  
HERBERG LJ, 1993, PHYSIOL BEHAV, V10, P617
[6]   The structure and functions of the cerebellum examined by a new method. [J].
Horsley, V ;
Clarke, RH .
BRAIN, 1908, 31 :45-124
[7]  
HOWARD CV, 1998, ROY MICRO S, V41, P1
[8]   HUMAN BRAIN SLICER - A METHOD FOR CUTTING CORONAL SLICES OF FRESH AND FIXED HUMAN BRAINS [J].
JACOBOWITZ, DM ;
SULLIVAN, JV ;
FITZE, PE .
BRAIN RESEARCH BULLETIN, 1994, 33 (04) :461-463
[9]   REMOVAL OF DISCRETE FRESH REGIONS OF RAT-BRAIN [J].
JACOBOWITZ, DM .
BRAIN RESEARCH, 1974, 80 (01) :111-115
[10]  
KAUFMANN JCE, 1979, ARCH PATHOL LAB MED, V103, P48