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Comparing stemness gene expression between stem cell subpopulations from peripheral blood and adipose tissue.

Authors :
González-Garza MT
Cruz-Vega DE
Cárdenas-Lopez A
de la Rosa RM
Moreno-Cuevas JE
Source :
American journal of stem cells [Am J Stem Cells] 2018 Jun 01; Vol. 7 (2), pp. 38-47. Date of Electronic Publication: 2018 Jun 01 (Print Publication: 2018).
Publication Year :
2018

Abstract

Cell therapy presents a promising alternative for the treatment of degenerative diseases. The main sources of adult stem cells are bone marrow, adipose tissue and peripheral blood. Within those tissues, there are cell subpopulations that share pluripotential characteristics. Nevertheless, there is insufficient data to determine which of these stem cell subtypes would have a better possibility to differentiate to a specific tissue. The objective of this research was to analyze and compare the stemness genes expression from peripheral blood and adipose tissue of plastic adherent cells, and those immune-selected by the CD133 <superscript>+</superscript> and CD271 <superscript>+</superscript> membrane markers. On all cell subpopulation groups, self-renew capacity, the membranes markers CD73, CD90 and CD105, as well as the stemness genes NANOG, OCT4, SOX2, REX1, NOTCH1 and, NESTIN expression were analyzed. Results showed that all samples presented the minimal criteria to define them as human stem cells. All cell subpopulation were capable of self-renewal. Nevertheless, the subpopulation cell types showed differences on the time needed to reach confluence. The slowest doubling times were for those cells bearing the CD133 marker from both sources. Surface markers determined by flow cytometry were positive for CD73, CD90 and, CD105, and negative for CD45. The stemness gene expression was positive in all subpopulation. However, there were significant differences in the amount and pattern of expression among them. Those differences could be advantageous in finding the best option for their application on cell therapy. Cells with high expression of OCT4 gene could be a better opportunity for neuron differentiation like CD133 <superscript>+</superscript> blood cells. On the other hand, lowest expression of NOTCH1 on CD271 <superscript>+</superscript> cells from the same source could be a better possibility for myoblast differentiation. The observed differences could be used as an advantage to find which cell type and from the different source; this represents the best option for its application on cell therapy. Experiments focused on the best response to specific differentiation, are conducted in order to confirm those possibilities.<br />Competing Interests: None.

Details

Language :
English
ISSN :
2160-4150
Volume :
7
Issue :
2
Database :
MEDLINE
Journal :
American journal of stem cells
Publication Type :
Academic Journal
Accession number :
29938124