Flow cytometry: a literature review
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFBA |
Texto Completo: | http://repositorio.ufba.br/ri/handle/ri/23238 |
Resumo: | Abstract Introduction: flow cytometry is a technique that employs an optical-electronic detection apparatus to analyze the physical and chemical properties of microscopic particles suspend in a liquid medium. Objective: to review the literature in search of the main studies that used flow cytometry as the main methodology. Method: Articles were selected according to their impact factor in the Journal of Citation Reports. Literature review: a light beam is direct to a continuous flow of suspended particles marked with fluorescent substances. The light is scattered differently from the beam by the particles and is captured by sensors in line and perpendicular to the light beam. These microscopic particles are conjugated with fluorescent substances that, once excited, emit light of lower frequency than the light source. The emitted light is captured by sensors and the particles are analyzed according to fluctuations in brightness of each detector and/or fluorescence emission. The result of this process is the formation of images in real time for each cell fluorescence, scattering and transmission of light. A major problem of flow cytometry is to determine whether a subset of cells labeled with fluorochrome-conjugated monoclonal antibodies is positive or negative. Gains compensation should be determined and applied correctly, and controls should be conducted concisely with the adoption of a biological control, isotype control or Fluorescence Minus One (FMO). None of these controls are considered ideal, and must be chosen according the number of different labeling done, rarity of molecule expression on surface or intracellularly in certain cell subsets, overlap of wavelengths or unspecific binding of the fluorochrome-conjugated antibodies. Conclusion: due to its great potential, flow cytometry has been expanded to diverse fields of biological sciences, and is routinely used in clinical diagnostic, biotechnology, and basic and applied research. Keywords: Flow cytometry. Monoclonal antibodies. Fluorochromes. |
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Errante, Paolo RuggeroEbbing, Pâmela Carolina CruzRodrigues, Francisco Sandro MenezesFerraz, Renato Ribeiro NogueiraSilva, Neusa Pereira daErrante, Paolo RuggeroEbbing, Pâmela Carolina CruzRodrigues, Francisco Sandro MenezesFerraz, Renato Ribeiro NogueiraSilva, Neusa Pereira da2017-06-20T15:15:23Z2017-06-20T15:15:23Z2015-05Rev. Ciênc. Méd. Biol., Salvador, v. 14, n. 2, p. 211-224, mai./ago. 20152236-5222http://repositorio.ufba.br/ri/handle/ri/23238v.14, n.2Abstract Introduction: flow cytometry is a technique that employs an optical-electronic detection apparatus to analyze the physical and chemical properties of microscopic particles suspend in a liquid medium. Objective: to review the literature in search of the main studies that used flow cytometry as the main methodology. Method: Articles were selected according to their impact factor in the Journal of Citation Reports. Literature review: a light beam is direct to a continuous flow of suspended particles marked with fluorescent substances. The light is scattered differently from the beam by the particles and is captured by sensors in line and perpendicular to the light beam. These microscopic particles are conjugated with fluorescent substances that, once excited, emit light of lower frequency than the light source. The emitted light is captured by sensors and the particles are analyzed according to fluctuations in brightness of each detector and/or fluorescence emission. The result of this process is the formation of images in real time for each cell fluorescence, scattering and transmission of light. A major problem of flow cytometry is to determine whether a subset of cells labeled with fluorochrome-conjugated monoclonal antibodies is positive or negative. Gains compensation should be determined and applied correctly, and controls should be conducted concisely with the adoption of a biological control, isotype control or Fluorescence Minus One (FMO). None of these controls are considered ideal, and must be chosen according the number of different labeling done, rarity of molecule expression on surface or intracellularly in certain cell subsets, overlap of wavelengths or unspecific binding of the fluorochrome-conjugated antibodies. Conclusion: due to its great potential, flow cytometry has been expanded to diverse fields of biological sciences, and is routinely used in clinical diagnostic, biotechnology, and basic and applied research. Keywords: Flow cytometry. Monoclonal antibodies. Fluorochromes.Introdução: a citometria de fluxo é uma técnica que utiliza um aparelho de detecção óptico-eletrônico para analisar as propriedades físicas e químicas das partículas microscópicas suspensas em meio líquido. Objetivo: revisar a literatura em busca dos principais estudos que utilizaram a citometria de fluxo como a metodologia principal. Método: os artigos foram selecionados de acordo com seu fator de impacto no Journal of Citation Reports. Revisão da literatura: um feixe de luz é dirigido para um fluxo contínuo de partículas suspensas marcadas com substâncias fluorescentes. A luz é difundida de forma diferente a partir do feixe de partículas e é capturada por meio de sensores em linha e perpendiculares ao feixe de luz. Tais partículas microscópicas são conjugadas com substâncias fluorescentes que emitem luz de frequência mais baixa do que a fonte de luz. A luz emitida é capturada por meio de sensores e as partículas são analisadas de acordo com flutuações de brilho de cada um dos detectores e/ou de emissão de fluorescência. O resultado deste processo é a formação de imagens em tempo real para cada célula da fluorescência, dispersão e transmissão de luz. Um dos principais problemas de citometria de fluxo é determinar se um subconjunto de células marcadas com anticorpos monoclonais conjugados com fluorocromos é positivo ou negativo. Ganhos de compensação devem ser determinados e aplicados corretamente, e os controles devem ser realizados de forma concisa, com a adoção de um controle biológico, controle de isotipo ou fluorescência menos uma (FMO). Nenhum desses controles é considerado ideal, e deve ser escolhido de acordo com o número de rotulagem, paucidade da expressão de moléculas na superfície ou no meio intracelular em determinadas subpopulações de células, sobreposição de comprimentos de onda ou ligação inespecífica dos anticorpos conjugados com fluorocromo. Conclusão: devido ao seu grande potencial, o uso da citometria de fluxo foi expandido para diversos campos das ciências biológicas, e é utilizada rotineiramente em clínicas de diagnóstico, e laboratórios de pesquisa básica e aplicada.Submitted by ROBERTO PAULO CORREIA DE ARAÚJO (ppgorgsistem@ufba.br) on 2017-06-20T15:15:23Z No. of bitstreams: 1 14_v.14_2.pdf: 1274141 bytes, checksum: 8ccf122ec2f1737496a03c99eda926f6 (MD5)Made available in DSpace on 2017-06-20T15:15:23Z (GMT). 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dc.title.pt_BR.fl_str_mv |
Flow cytometry: a literature review |
dc.title.alternative.pt_BR.fl_str_mv |
Revista de Ciências Médicas e Biológicas |
title |
Flow cytometry: a literature review |
spellingShingle |
Flow cytometry: a literature review Errante, Paolo Ruggero Citometria de fluxo. Anticorpos monoclonais. Fluorocromos. |
title_short |
Flow cytometry: a literature review |
title_full |
Flow cytometry: a literature review |
title_fullStr |
Flow cytometry: a literature review |
title_full_unstemmed |
Flow cytometry: a literature review |
title_sort |
Flow cytometry: a literature review |
author |
Errante, Paolo Ruggero |
author_facet |
Errante, Paolo Ruggero Ebbing, Pâmela Carolina Cruz Rodrigues, Francisco Sandro Menezes Ferraz, Renato Ribeiro Nogueira Silva, Neusa Pereira da |
author_role |
author |
author2 |
Ebbing, Pâmela Carolina Cruz Rodrigues, Francisco Sandro Menezes Ferraz, Renato Ribeiro Nogueira Silva, Neusa Pereira da |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Errante, Paolo Ruggero Ebbing, Pâmela Carolina Cruz Rodrigues, Francisco Sandro Menezes Ferraz, Renato Ribeiro Nogueira Silva, Neusa Pereira da Errante, Paolo Ruggero Ebbing, Pâmela Carolina Cruz Rodrigues, Francisco Sandro Menezes Ferraz, Renato Ribeiro Nogueira Silva, Neusa Pereira da |
dc.subject.por.fl_str_mv |
Citometria de fluxo. Anticorpos monoclonais. Fluorocromos. |
topic |
Citometria de fluxo. Anticorpos monoclonais. Fluorocromos. |
description |
Abstract Introduction: flow cytometry is a technique that employs an optical-electronic detection apparatus to analyze the physical and chemical properties of microscopic particles suspend in a liquid medium. Objective: to review the literature in search of the main studies that used flow cytometry as the main methodology. Method: Articles were selected according to their impact factor in the Journal of Citation Reports. Literature review: a light beam is direct to a continuous flow of suspended particles marked with fluorescent substances. The light is scattered differently from the beam by the particles and is captured by sensors in line and perpendicular to the light beam. These microscopic particles are conjugated with fluorescent substances that, once excited, emit light of lower frequency than the light source. The emitted light is captured by sensors and the particles are analyzed according to fluctuations in brightness of each detector and/or fluorescence emission. The result of this process is the formation of images in real time for each cell fluorescence, scattering and transmission of light. A major problem of flow cytometry is to determine whether a subset of cells labeled with fluorochrome-conjugated monoclonal antibodies is positive or negative. Gains compensation should be determined and applied correctly, and controls should be conducted concisely with the adoption of a biological control, isotype control or Fluorescence Minus One (FMO). None of these controls are considered ideal, and must be chosen according the number of different labeling done, rarity of molecule expression on surface or intracellularly in certain cell subsets, overlap of wavelengths or unspecific binding of the fluorochrome-conjugated antibodies. Conclusion: due to its great potential, flow cytometry has been expanded to diverse fields of biological sciences, and is routinely used in clinical diagnostic, biotechnology, and basic and applied research. Keywords: Flow cytometry. Monoclonal antibodies. Fluorochromes. |
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2015 |
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2015-05 |
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2017-06-20T15:15:23Z |
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2017-06-20T15:15:23Z |
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dc.identifier.citation.fl_str_mv |
Rev. Ciênc. Méd. Biol., Salvador, v. 14, n. 2, p. 211-224, mai./ago. 2015 |
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http://repositorio.ufba.br/ri/handle/ri/23238 |
dc.identifier.issn.none.fl_str_mv |
2236-5222 |
dc.identifier.number.pt_BR.fl_str_mv |
v.14, n.2 |
identifier_str_mv |
Rev. Ciênc. Méd. Biol., Salvador, v. 14, n. 2, p. 211-224, mai./ago. 2015 2236-5222 v.14, n.2 |
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http://repositorio.ufba.br/ri/handle/ri/23238 |
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por |
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Instituto de Ciências da Saúde/ Universidade Federal da Bahia |
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Brasil |
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Instituto de Ciências da Saúde/ Universidade Federal da Bahia |
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http://www.portalseer.ufba.br/index.php/cmbio/article/view/12182/10845 |
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