Tissue microarrays in the study of non-neoplastic disease of the nervous system

被引:18
作者
Goldstine, J
Seligson, DB
Beizai, P
Miyata, H
Vinters, HV
机构
[1] Univ Calif Los Angeles, Dept Pathol & Lab Med Neuropathol, Ctr Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sect Neuropathol, Ctr Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Neurol, Ctr Med, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Brain Res Inst, Ctr Med, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Inst Neuropsychiat, Ctr Med, Los Angeles, CA 90095 USA
[6] Tottori Univ, Dept Neuropathol, Inst Neurol Sci, Yonago, Tottori, Japan
关键词
AIDS (acquired immunodeficiency syndrome); Alzheimer disease; HIV-1; infection; immunohistochemistry; CNS infections; neurodegenerative diseases; tissue microarrays;
D O I
10.1093/jnen/61.8.653
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Tissue microarrays (TMAs), also known as "tissue chips," are a recently developed method that allows small cores or discs of tissue from dozens or hundreds of (usually paraffin-embedded) specimens to be re-embedded in a tissue block, which can then be further sectioned. The tissue cores can subsequently be studied using any combination of techniques, including immunohistochemistry, in situ hybridization (ISH), fluorescence ISH, and in situ polymerase chain reaction (PCR). To date, the technique has found greatest use in the analysis of neoplasms, including gliomas. We describe, and provide examples of, how TMAs might be utilized in investigation of autopsy (or biopsy) tissues from individuals with non-neoplastic disease, especially to address questions that require systematic review of multiple (nearly) identical brain regions across dozens or hundreds of cases. Specific questions related to patterns of protein expression (e.g. tau, Abeta, alpha-synuclein) in multiple regions of large numbers of brain specimens (from patients with neurodegenerative diseases) can be efficiently examined using TMA technology. One possible use of TMAs in the area of infectious disease might be to examine patterns of HIV-related brain injury or AIDS-related opportunistic CNS infections in the epochs before and after highly active antiretroviral therapy came into widespread use.
引用
收藏
页码:653 / 662
页数:10
相关论文
共 53 条
[1]  
Achim C L, 1996, J NeuroAIDS, V1, P1, DOI 10.1300/J128v01n02_01
[2]   Early entry and widespread cellular involvement of HIV-1 DNA in brains of HIV-1 positive asymptomatic individuals [J].
An, SF ;
Groves, M ;
Gray, F ;
Scaravilli, F .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1999, 58 (11) :1156-1162
[3]  
ANDERS KH, 1986, AM J PATHOL, V124, P537
[4]  
Andersen CL, 2001, CYTOMETRY, V45, P83, DOI 10.1002/1097-0320(20011001)45:2<83::AID-CYTO1149>3.0.CO
[5]  
2-P
[6]   HUMAN-IMMUNODEFICIENCY-VIRUS AND THE BRAIN - INVESTIGATION OF VIRUS LOAD AND NEUROPATHOLOGIC CHANGES IN PRE-AIDS SUBJECTS [J].
BELL, JE ;
BUSUTTIL, A ;
IRONSIDE, JW ;
REBUS, S ;
DONALDSON, YK ;
SIMMONDS, P ;
PEUTHERER, JF .
JOURNAL OF INFECTIOUS DISEASES, 1993, 168 (04) :818-824
[7]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[8]   Tissue microarray (TMA) technology:: miniaturized pathology archives for high-throughput in situ studies [J].
Bubendorf, L ;
Nocito, A ;
Moch, H ;
Sauter, G .
JOURNAL OF PATHOLOGY, 2001, 195 (01) :72-79
[9]   BRAIN PATHOLOGY INDUCED BY INFECTION WITH THE HUMAN IMMUNODEFICIENCY VIRUS (HIV) - A HISTOLOGICAL, IMMUNOCYTOCHEMICAL, AND ELECTRON MICROSCOPICAL STUDY OF 100 AUTOPSY CASES [J].
BUDKA, H ;
COSTANZI, G ;
CRISTINA, S ;
LECHI, A ;
PARRAVICINI, C ;
TRABATTONI, R ;
VAGO, L .
ACTA NEUROPATHOLOGICA, 1987, 75 (02) :185-198
[10]  
CRINO PB, 2002, IN PRESS BRAIN PATHO