Amniotic Fluid Cells Proliferation in Normal and Down Syndrome Subjects

Down Syndrome/Trisomy 21 is the most common chromosomal anomaly, and it represents the most common congenital cause of infants’ intellectual disability. Subjects with this syndrome are affected by degenerative processes caused by accelerated aging or unknown ethyologies. In recent years, accumulatin...

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Main Authors: Honcea Adina, Iulian R., Pavel Anca Gabriela, Ion Ileana, Sima Livia Elena
Format: Article
Language:English
Published: Sciendo 2016-02-01
Series:ARS Medica Tomitana
Subjects:
Online Access:https://doi.org/10.1515/arsm-2016-0001
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spelling doaj-00627f4fe5664153ad567dc8305672f42021-09-06T19:40:04ZengSciendoARS Medica Tomitana1841-40362016-02-012211910.1515/arsm-2016-0001arsm-2016-0001Amniotic Fluid Cells Proliferation in Normal and Down Syndrome SubjectsHoncea Adina0Iulian R.1Pavel Anca Gabriela2Ion Ileana3Sima Livia Elena4 University “Ovidius” of Constanta Genetic Lab, Bucharest Cytogenomic, Bucharest University “Ovidius” of Constanta Molecular Cell Biology Department, Institute of Biochemistry of the Romanian Academy, BucharestDown Syndrome/Trisomy 21 is the most common chromosomal anomaly, and it represents the most common congenital cause of infants’ intellectual disability. Subjects with this syndrome are affected by degenerative processes caused by accelerated aging or unknown ethyologies. In recent years, accumulating evidence revealed increased potential of amniotic fluid-derived stem cells to be used in regenerative therapy. Our aim was to assess differences in immunophenotype, cell morphology and proliferation of amniotic fluid cells from normal and Down Syndrome pregnancies using a quantitative cytometry approach. Results revealed the emergence of a population of small sized cells in Down Syndrome derived amniotic fluid cells that are readily visible upon microscopic inspection. Hence, the fluorescence–based quantitative image cytometry determinations showed a tendency of decrease in both cell and nuclei size in trisomy, with no significant modification in nuclei circularity, as measured following actin cytoskeleton and nuclei labeling. The propensity of Ki67 positive cells was found to be increased in Down Syndrome derived cells (48.92%) as compared to normal specimens (28.68%). However, cells in S and G2/M cell cycle phases decreased from 32.91% to 4.49% in diseased cells. Further studies are devoted to understanding the molecular basis of the observed differences in the proliferation ability of Down Syndrome amniotic cells, in order to evaluate the potential therapeutic effect of amniotic fluid stem cells for tissue regeneration in subjects with trisomy and to find correlations between amniotic cells phenotype and patient prognosis.https://doi.org/10.1515/arsm-2016-0001down syndrometrisomy 21amniotic fluid-derived stem cellsproliferationcell cycle
collection DOAJ
language English
format Article
sources DOAJ
author Honcea Adina
Iulian R.
Pavel Anca Gabriela
Ion Ileana
Sima Livia Elena
spellingShingle Honcea Adina
Iulian R.
Pavel Anca Gabriela
Ion Ileana
Sima Livia Elena
Amniotic Fluid Cells Proliferation in Normal and Down Syndrome Subjects
ARS Medica Tomitana
down syndrome
trisomy 21
amniotic fluid-derived stem cells
proliferation
cell cycle
author_facet Honcea Adina
Iulian R.
Pavel Anca Gabriela
Ion Ileana
Sima Livia Elena
author_sort Honcea Adina
title Amniotic Fluid Cells Proliferation in Normal and Down Syndrome Subjects
title_short Amniotic Fluid Cells Proliferation in Normal and Down Syndrome Subjects
title_full Amniotic Fluid Cells Proliferation in Normal and Down Syndrome Subjects
title_fullStr Amniotic Fluid Cells Proliferation in Normal and Down Syndrome Subjects
title_full_unstemmed Amniotic Fluid Cells Proliferation in Normal and Down Syndrome Subjects
title_sort amniotic fluid cells proliferation in normal and down syndrome subjects
publisher Sciendo
series ARS Medica Tomitana
issn 1841-4036
publishDate 2016-02-01
description Down Syndrome/Trisomy 21 is the most common chromosomal anomaly, and it represents the most common congenital cause of infants’ intellectual disability. Subjects with this syndrome are affected by degenerative processes caused by accelerated aging or unknown ethyologies. In recent years, accumulating evidence revealed increased potential of amniotic fluid-derived stem cells to be used in regenerative therapy. Our aim was to assess differences in immunophenotype, cell morphology and proliferation of amniotic fluid cells from normal and Down Syndrome pregnancies using a quantitative cytometry approach. Results revealed the emergence of a population of small sized cells in Down Syndrome derived amniotic fluid cells that are readily visible upon microscopic inspection. Hence, the fluorescence–based quantitative image cytometry determinations showed a tendency of decrease in both cell and nuclei size in trisomy, with no significant modification in nuclei circularity, as measured following actin cytoskeleton and nuclei labeling. The propensity of Ki67 positive cells was found to be increased in Down Syndrome derived cells (48.92%) as compared to normal specimens (28.68%). However, cells in S and G2/M cell cycle phases decreased from 32.91% to 4.49% in diseased cells. Further studies are devoted to understanding the molecular basis of the observed differences in the proliferation ability of Down Syndrome amniotic cells, in order to evaluate the potential therapeutic effect of amniotic fluid stem cells for tissue regeneration in subjects with trisomy and to find correlations between amniotic cells phenotype and patient prognosis.
topic down syndrome
trisomy 21
amniotic fluid-derived stem cells
proliferation
cell cycle
url https://doi.org/10.1515/arsm-2016-0001
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AT ionileana amnioticfluidcellsproliferationinnormalanddownsyndromesubjects
AT simaliviaelena amnioticfluidcellsproliferationinnormalanddownsyndromesubjects
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