Variable expressivity of the tumour suppressor protein TRP53 in cryopreserved human blastocysts

<p>Abstract</p> <p>In a mouse model, in vitro fertilization or extended embryo culture leads to the increased expression of TRP53 in susceptible embryos. Ablation of the TRP53 gene improved embryo viability indicating that increased expression of TRP53 is a cause of the reduction o...

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Main Authors: Stojanov Tomas, Chami Omar, Chandrakanthan Vashe, O'Neill Chris
Format: Article
Language:English
Published: BMC 2007-10-01
Series:Reproductive Biology and Endocrinology
Online Access:http://www.rbej.com/content/5/1/39
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spelling doaj-4dc889f54230481da882589467df62182020-11-24T22:19:34ZengBMCReproductive Biology and Endocrinology1477-78272007-10-01513910.1186/1477-7827-5-39Variable expressivity of the tumour suppressor protein TRP53 in cryopreserved human blastocystsStojanov TomasChami OmarChandrakanthan VasheO'Neill Chris<p>Abstract</p> <p>In a mouse model, in vitro fertilization or extended embryo culture leads to the increased expression of TRP53 in susceptible embryos. Ablation of the TRP53 gene improved embryo viability indicating that increased expression of TRP53 is a cause of the reduction of embryo viability resulting from in vitro fertilization or embryo culture. This study investigates the status of TRP53 expression in human embryos produced by intracytoplasmic sperm injection. Following fertilization, embryos were cultured for 96 h and then cryopreserved. Immediately upon thawing they were fixed in formaldehyde and subjected to immunostaining for TRP53. Staining was visualized by confocal microscopy. Negative controls were incubated with isotype control immunoglobulin and showed negligible staining. All embryos showed TRP53 staining above negative controls. TRP53 staining was heterogenous within and between embryos. An embryo that showed retarded development showed high levels of TRP53 expression. A blastocyst that had a collapsed blastocoel also showed high levels of TRP53 compared to morphologically normal blastocysts. Most TRP53 staining was in the region of the nucleus. Morphologically normal blastocysts tended to show little nuclear accumulation of stain. However, some cells within these embryos had high levels of nuclear TRP53 expression. The results show that embryos have varying sensitivity to the stresses of production and culture in vitro, and this resulted in variable expressivity of TRP53.</p> http://www.rbej.com/content/5/1/39
collection DOAJ
language English
format Article
sources DOAJ
author Stojanov Tomas
Chami Omar
Chandrakanthan Vashe
O'Neill Chris
spellingShingle Stojanov Tomas
Chami Omar
Chandrakanthan Vashe
O'Neill Chris
Variable expressivity of the tumour suppressor protein TRP53 in cryopreserved human blastocysts
Reproductive Biology and Endocrinology
author_facet Stojanov Tomas
Chami Omar
Chandrakanthan Vashe
O'Neill Chris
author_sort Stojanov Tomas
title Variable expressivity of the tumour suppressor protein TRP53 in cryopreserved human blastocysts
title_short Variable expressivity of the tumour suppressor protein TRP53 in cryopreserved human blastocysts
title_full Variable expressivity of the tumour suppressor protein TRP53 in cryopreserved human blastocysts
title_fullStr Variable expressivity of the tumour suppressor protein TRP53 in cryopreserved human blastocysts
title_full_unstemmed Variable expressivity of the tumour suppressor protein TRP53 in cryopreserved human blastocysts
title_sort variable expressivity of the tumour suppressor protein trp53 in cryopreserved human blastocysts
publisher BMC
series Reproductive Biology and Endocrinology
issn 1477-7827
publishDate 2007-10-01
description <p>Abstract</p> <p>In a mouse model, in vitro fertilization or extended embryo culture leads to the increased expression of TRP53 in susceptible embryos. Ablation of the TRP53 gene improved embryo viability indicating that increased expression of TRP53 is a cause of the reduction of embryo viability resulting from in vitro fertilization or embryo culture. This study investigates the status of TRP53 expression in human embryos produced by intracytoplasmic sperm injection. Following fertilization, embryos were cultured for 96 h and then cryopreserved. Immediately upon thawing they were fixed in formaldehyde and subjected to immunostaining for TRP53. Staining was visualized by confocal microscopy. Negative controls were incubated with isotype control immunoglobulin and showed negligible staining. All embryos showed TRP53 staining above negative controls. TRP53 staining was heterogenous within and between embryos. An embryo that showed retarded development showed high levels of TRP53 expression. A blastocyst that had a collapsed blastocoel also showed high levels of TRP53 compared to morphologically normal blastocysts. Most TRP53 staining was in the region of the nucleus. Morphologically normal blastocysts tended to show little nuclear accumulation of stain. However, some cells within these embryos had high levels of nuclear TRP53 expression. The results show that embryos have varying sensitivity to the stresses of production and culture in vitro, and this resulted in variable expressivity of TRP53.</p>
url http://www.rbej.com/content/5/1/39
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AT chamiomar variableexpressivityofthetumoursuppressorproteintrp53incryopreservedhumanblastocysts
AT chandrakanthanvashe variableexpressivityofthetumoursuppressorproteintrp53incryopreservedhumanblastocysts
AT oneillchris variableexpressivityofthetumoursuppressorproteintrp53incryopreservedhumanblastocysts
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