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Human Cells Display Reduced Apoptotic Function Relative to Chimpanzee Cells
Previously published gene expression analyses suggested that apoptotic function may be reduced in humans relative to chimpanzees and led to the hypothesis that this difference may contribute to the relatively larger size of the human brain and the increased propensity of humans to develop cancer. In...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460825/ https://www.ncbi.nlm.nih.gov/pubmed/23029431 http://dx.doi.org/10.1371/journal.pone.0046182 |
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author | Arora, Gaurav Mezencev, Roman McDonald, John F. |
author_facet | Arora, Gaurav Mezencev, Roman McDonald, John F. |
author_sort | Arora, Gaurav |
collection | PubMed |
description | Previously published gene expression analyses suggested that apoptotic function may be reduced in humans relative to chimpanzees and led to the hypothesis that this difference may contribute to the relatively larger size of the human brain and the increased propensity of humans to develop cancer. In this study, we sought to further test the hypothesis that humans maintain a reduced apoptotic function relative to chimpanzees by conducting a series of apoptotic function assays on human, chimpanzee and macaque primary fibroblastic cells. Human cells consistently displayed significantly reduced apoptotic function relative to the chimpanzee and macaque cells. These results are consistent with earlier findings indicating that apoptotic function is reduced in humans relative to chimpanzees. |
format | Online Article Text |
id | pubmed-3460825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34608252012-10-01 Human Cells Display Reduced Apoptotic Function Relative to Chimpanzee Cells Arora, Gaurav Mezencev, Roman McDonald, John F. PLoS One Research Article Previously published gene expression analyses suggested that apoptotic function may be reduced in humans relative to chimpanzees and led to the hypothesis that this difference may contribute to the relatively larger size of the human brain and the increased propensity of humans to develop cancer. In this study, we sought to further test the hypothesis that humans maintain a reduced apoptotic function relative to chimpanzees by conducting a series of apoptotic function assays on human, chimpanzee and macaque primary fibroblastic cells. Human cells consistently displayed significantly reduced apoptotic function relative to the chimpanzee and macaque cells. These results are consistent with earlier findings indicating that apoptotic function is reduced in humans relative to chimpanzees. Public Library of Science 2012-09-28 /pmc/articles/PMC3460825/ /pubmed/23029431 http://dx.doi.org/10.1371/journal.pone.0046182 Text en © 2012 Arora et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Arora, Gaurav Mezencev, Roman McDonald, John F. Human Cells Display Reduced Apoptotic Function Relative to Chimpanzee Cells |
title | Human Cells Display Reduced Apoptotic Function Relative to Chimpanzee Cells |
title_full | Human Cells Display Reduced Apoptotic Function Relative to Chimpanzee Cells |
title_fullStr | Human Cells Display Reduced Apoptotic Function Relative to Chimpanzee Cells |
title_full_unstemmed | Human Cells Display Reduced Apoptotic Function Relative to Chimpanzee Cells |
title_short | Human Cells Display Reduced Apoptotic Function Relative to Chimpanzee Cells |
title_sort | human cells display reduced apoptotic function relative to chimpanzee cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460825/ https://www.ncbi.nlm.nih.gov/pubmed/23029431 http://dx.doi.org/10.1371/journal.pone.0046182 |
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