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Protein Analysis in Human Cerebrospinal Fluid: Physiological Aspects, Current Progress and Future Challenges
The introduction of lumbar puncture into clinical medicine over 100 years ago marks the beginning of the study of central nervous system diseases using the human cerebrospinal fluid (CSF). Ever since, CSF has been analyzed extensively to elucidate the physiological and biochemical bases of neurologi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850820/ https://www.ncbi.nlm.nih.gov/pubmed/16410649 http://dx.doi.org/10.1155/2006/158797 |
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author | Hühmer, Andreas F. Biringer, Roger G. Amato, Heidi Fonteh, Alfred N. Harrington, Michael G. |
author_facet | Hühmer, Andreas F. Biringer, Roger G. Amato, Heidi Fonteh, Alfred N. Harrington, Michael G. |
author_sort | Hühmer, Andreas F. |
collection | PubMed |
description | The introduction of lumbar puncture into clinical medicine over 100 years ago marks the beginning of the study of central nervous system diseases using the human cerebrospinal fluid (CSF). Ever since, CSF has been analyzed extensively to elucidate the physiological and biochemical bases of neurological disease. The proximity of CSF to the brain makes it a good target for studying the pathophysiology of brain functions, but the barrier function of the CSF also impedes its diagnostic value. Today, measurements to determine alterations in the composition of CSF are central in the differential diagnosis of specific diseases of the central nervous system (CNS). In particular, the analysis of the CSF protein composition provides crucial information in the diagnosis of CNS diseases. This enables the assessment of the physiology of the blood-CSF barrier and of the immunology of intrathecial responses. Besides those routine measurements, protein compositional studies of CSF have been extended recently to many other proteins in the expectation that comprehensive analysis of lower abundance CSF proteins will lead to the discovery of new disease markers. Disease marker discovery by molecular profiling of the CSF tissue has the enormous potential of providing many new disease relevant molecules. New developments in protein profiling techniques hold promise for the discovery and validation of relevant disease markers. In this review, we summarize the current efforts and progress in CSF protein profiling measurements using conventional and current protein analysis tools. We also discuss necessary development in methodology in order to have the highest impact on the study of the molecular composition of CSF proteins. |
format | Online Article Text |
id | pubmed-3850820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38508202013-12-18 Protein Analysis in Human Cerebrospinal Fluid: Physiological Aspects, Current Progress and Future Challenges Hühmer, Andreas F. Biringer, Roger G. Amato, Heidi Fonteh, Alfred N. Harrington, Michael G. Dis Markers Other The introduction of lumbar puncture into clinical medicine over 100 years ago marks the beginning of the study of central nervous system diseases using the human cerebrospinal fluid (CSF). Ever since, CSF has been analyzed extensively to elucidate the physiological and biochemical bases of neurological disease. The proximity of CSF to the brain makes it a good target for studying the pathophysiology of brain functions, but the barrier function of the CSF also impedes its diagnostic value. Today, measurements to determine alterations in the composition of CSF are central in the differential diagnosis of specific diseases of the central nervous system (CNS). In particular, the analysis of the CSF protein composition provides crucial information in the diagnosis of CNS diseases. This enables the assessment of the physiology of the blood-CSF barrier and of the immunology of intrathecial responses. Besides those routine measurements, protein compositional studies of CSF have been extended recently to many other proteins in the expectation that comprehensive analysis of lower abundance CSF proteins will lead to the discovery of new disease markers. Disease marker discovery by molecular profiling of the CSF tissue has the enormous potential of providing many new disease relevant molecules. New developments in protein profiling techniques hold promise for the discovery and validation of relevant disease markers. In this review, we summarize the current efforts and progress in CSF protein profiling measurements using conventional and current protein analysis tools. We also discuss necessary development in methodology in order to have the highest impact on the study of the molecular composition of CSF proteins. IOS Press 2006 2005-12-22 /pmc/articles/PMC3850820/ /pubmed/16410649 http://dx.doi.org/10.1155/2006/158797 Text en Copyright © 2006 Hindawi Publishing Corporation. |
spellingShingle | Other Hühmer, Andreas F. Biringer, Roger G. Amato, Heidi Fonteh, Alfred N. Harrington, Michael G. Protein Analysis in Human Cerebrospinal Fluid: Physiological Aspects, Current Progress and Future Challenges |
title | Protein Analysis in Human Cerebrospinal Fluid: Physiological Aspects, Current Progress and Future Challenges |
title_full | Protein Analysis in Human Cerebrospinal Fluid: Physiological Aspects, Current Progress and Future Challenges |
title_fullStr | Protein Analysis in Human Cerebrospinal Fluid: Physiological Aspects, Current Progress and Future Challenges |
title_full_unstemmed | Protein Analysis in Human Cerebrospinal Fluid: Physiological Aspects, Current Progress and Future Challenges |
title_short | Protein Analysis in Human Cerebrospinal Fluid: Physiological Aspects, Current Progress and Future Challenges |
title_sort | protein analysis in human cerebrospinal fluid: physiological aspects, current progress and future challenges |
topic | Other |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850820/ https://www.ncbi.nlm.nih.gov/pubmed/16410649 http://dx.doi.org/10.1155/2006/158797 |
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