Neurofilament triplet proteins are restricted to a subset of neurons in the rat neocortex

被引:60
作者
Kirkcaldie, MTK
Dickson, TC
King, CE
Grasby, D
Riederer, BM
Vickers, JC
机构
[1] Univ Tasmania, Discipline Pathol, Hobart, Tas 7001, Australia
[2] Univ Newcastle, Sch Biomed Sci, Callaghan, NSW 2308, Australia
[3] Inst Biol Cellulaire & Morphol, CH-1005 Lausanne, Switzerland
基金
澳大利亚研究理事会; 英国医学研究理事会; 美国国家科学基金会;
关键词
cytoskeleton; phenotype; cytoarchitecture; development; myelination;
D O I
10.1016/S0891-0618(02)00043-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cellular localisation of neurofilament triplet subunits was investigated in the rat neocortex. A subset of mainly pyramidal neurons showed colocalisation of subunit immunolabelling throughout the neocortex, including labelling with the antibody SMI32, which has been used extensively in other studies of the primate cortex as a selective cellular marker. Neurofilament-labelled neurons were principally localised to two or three cell layers in most cortical regions, but dramatically reduced labelling was present in areas such as the perirhinal cortex, anterior cingulate and a strip of cortex extending from caudal motor regions through the medial parietal region to secondary visual areas. However, quantitative analysis demonstrated a similar proportion (10-20%) of cells with neurofilament triplet labelling in regions of high or low labelling. Combining retrograde tracing with immunolabelling showed that cellular content of the neurofilament proteins Was not correlated with the length of projection. Double labelling immunohistochemistry demonstrated that neurofilament content in axons was closely associated with myelination. Analysis of SMI32 labelling in development indicated that content of this epitope within cell bodies was associated with relatively late maturation, between postnatal days 14 and 21. This study is further evidence of a cell type-specific regulation of neurofilament proteins within neocortical neurons. Neurofilament triplet content may be more closely related to the degree of myelination, rather than the absolute length, of the projecting axon. Crown Copyright (C) 2002 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:163 / 171
页数:9
相关论文
共 46 条
[31]  
PAXINOS G, 1999, CHEMOARCHITECTONIC A
[32]   SOLUBILITY OF CYTOSKELETAL PROTEINS IN IMMUNOHISTOCHEMISTRY AND THE INFLUENCE OF FIXATION [J].
RIEDERER, BM ;
PORCHET, R ;
MARUGG, RA ;
BINDER, LI .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1993, 41 (04) :609-616
[33]  
RIEDERER BM, 1996, EUR J NEUROSCI, P33
[34]  
SHAW G, 1991, NEURONAL CYTOSKELETO, P185
[35]   MONOCLONAL-ANTIBODIES DISTINGUISH PHOSPHORYLATED AND NONPHOSPHORYLATED FORMS OF NEUROFILAMENTS INSITU [J].
STERNBERGER, LA ;
STERNBERGER, NH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (19) :6126-6130
[36]   A NEUROFILAMENT PROTEIN ANTIBODY SELECTIVELY LABELS A LARGE GANGLION-CELL TYPE IN THE HUMAN RETINA [J].
STRAZNICKY, C ;
VICKERS, JC ;
GABRIEL, R ;
COSTA, M .
BRAIN RESEARCH, 1992, 582 (01) :123-128
[37]   PHOSPHORYLATION-DEPENDENT EPITOPES ON NEUROFILAMENT PROTEINS AND NEUROFILAMENT DENSITIES DIFFER IN AXONS IN THE CORTICOSPINAL AND PRIMARY SENSORY DORSAL COLUMN TRACTS IN THE RAT SPINAL-CORD [J].
SZARO, BG ;
WHITNALL, MH ;
GAINER, H .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 302 (02) :220-235
[38]   Motor neurons are rich in non-phosphorylated neurofilaments: cross-species comparison and alterations in ALS [J].
Tsang, YM ;
Chiong, F ;
Kuznetsov, D ;
Kasarskis, E ;
Geula, C .
BRAIN RESEARCH, 2000, 861 (01) :45-58
[39]   Neurofilament protein: A selective marker for the architectonic parcellation of the visual cortex in adult cat brain [J].
Van der Gucht, E ;
Vandesande, F ;
Arckens, L .
JOURNAL OF COMPARATIVE NEUROLOGY, 2001, 441 (04) :345-368
[40]   The cause of neuronal degeneration in Alzheimer's disease [J].
Vickers, JC ;
Dickson, TC ;
Adlard, PA ;
Saunders, HL ;
King, CE ;
McCormack, G .
PROGRESS IN NEUROBIOLOGY, 2000, 60 (02) :139-165