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Apoptosis-Specific Protein (ASP) Identified in Apoptotic Xenopus Thymus Tumor Cells
A novel apoptosis-specific protein (ASP) has recently been identified in the cytoplasm of apoptotic mammalian cells. This paper investigates whether ASP is found in Xenopus thymus tumor-derived lymphoid cell lines undergoing apoptosis and also in apoptotic, nontransformed splenocytes. Cultured Xenop...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275995/ https://www.ncbi.nlm.nih.gov/pubmed/9814588 http://dx.doi.org/10.1155/1998/70616 |
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author | Horton, John Milner, Anne Horton, Trudy Ritchie, Pamela Gascoyne, Duncan Hewson, Tim Hammond, Ester Gregory, Christopher Grand, Roger |
author_facet | Horton, John Milner, Anne Horton, Trudy Ritchie, Pamela Gascoyne, Duncan Hewson, Tim Hammond, Ester Gregory, Christopher Grand, Roger |
author_sort | Horton, John |
collection | PubMed |
description | A novel apoptosis-specific protein (ASP) has recently been identified in the cytoplasm of apoptotic mammalian cells. This paper investigates whether ASP is found in Xenopus thymus tumor-derived lymphoid cell lines undergoing apoptosis and also in apoptotic, nontransformed splenocytes. Cultured Xenopus tumor lymphoid cells induced to undergo, apoptosis by serum deprivation or treatment with the calcium ionophore, ionomycin, displayed altered morphology typical of apoptotic cells, as judged by flow cytometric light-scatter characteristics and by fluorescence microscopy of acridine-orange-stained cells. Flow cytometry of permeabilized cells and fluorescence microscopy of acetone-fixed cytospins revealed that apoptotic Xenopus tumor cells, especially those displaying loss or condensation of DNA, displayed increased expression of epitopes recognized by a rabbit polyclonal antibody against ASP. Flow cytometry confirmed that ASP is also expressed in splenocytes induced to apoptose by culture in ionomycin or following concanavalin A stimulation. No increased expression of ASP was seen when lymphoid tumor cells or splenocytes were induced into necrosis by overdose with the antifungal agent amphotericin B. Western blotting with antibody against ASP identified the emergence of several protein bands in cell lysates from apoptotic, but not necrotic, Xenopus tumor cells. The new and simple methodology for identifying apoptotic cells described here is likely to be of value to those studying immune system development and associated programmed cell death in Xenopus. |
format | Text |
id | pubmed-2275995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-22759952008-03-31 Apoptosis-Specific Protein (ASP) Identified in Apoptotic Xenopus Thymus Tumor Cells Horton, John Milner, Anne Horton, Trudy Ritchie, Pamela Gascoyne, Duncan Hewson, Tim Hammond, Ester Gregory, Christopher Grand, Roger Dev Immunol Research Article A novel apoptosis-specific protein (ASP) has recently been identified in the cytoplasm of apoptotic mammalian cells. This paper investigates whether ASP is found in Xenopus thymus tumor-derived lymphoid cell lines undergoing apoptosis and also in apoptotic, nontransformed splenocytes. Cultured Xenopus tumor lymphoid cells induced to undergo, apoptosis by serum deprivation or treatment with the calcium ionophore, ionomycin, displayed altered morphology typical of apoptotic cells, as judged by flow cytometric light-scatter characteristics and by fluorescence microscopy of acridine-orange-stained cells. Flow cytometry of permeabilized cells and fluorescence microscopy of acetone-fixed cytospins revealed that apoptotic Xenopus tumor cells, especially those displaying loss or condensation of DNA, displayed increased expression of epitopes recognized by a rabbit polyclonal antibody against ASP. Flow cytometry confirmed that ASP is also expressed in splenocytes induced to apoptose by culture in ionomycin or following concanavalin A stimulation. No increased expression of ASP was seen when lymphoid tumor cells or splenocytes were induced into necrosis by overdose with the antifungal agent amphotericin B. Western blotting with antibody against ASP identified the emergence of several protein bands in cell lysates from apoptotic, but not necrotic, Xenopus tumor cells. The new and simple methodology for identifying apoptotic cells described here is likely to be of value to those studying immune system development and associated programmed cell death in Xenopus. Hindawi Publishing Corporation 1998 /pmc/articles/PMC2275995/ /pubmed/9814588 http://dx.doi.org/10.1155/1998/70616 Text en Copyright © 1998 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Horton, John Milner, Anne Horton, Trudy Ritchie, Pamela Gascoyne, Duncan Hewson, Tim Hammond, Ester Gregory, Christopher Grand, Roger Apoptosis-Specific Protein (ASP) Identified in Apoptotic Xenopus Thymus Tumor Cells |
title | Apoptosis-Specific Protein (ASP) Identified in Apoptotic Xenopus Thymus Tumor Cells |
title_full | Apoptosis-Specific Protein (ASP) Identified in Apoptotic Xenopus Thymus Tumor Cells |
title_fullStr | Apoptosis-Specific Protein (ASP) Identified in Apoptotic Xenopus Thymus Tumor Cells |
title_full_unstemmed | Apoptosis-Specific Protein (ASP) Identified in Apoptotic Xenopus Thymus Tumor Cells |
title_short | Apoptosis-Specific Protein (ASP) Identified in Apoptotic Xenopus Thymus Tumor Cells |
title_sort | apoptosis-specific protein (asp) identified in apoptotic xenopus thymus tumor cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275995/ https://www.ncbi.nlm.nih.gov/pubmed/9814588 http://dx.doi.org/10.1155/1998/70616 |
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