Issue 6, 2015

Comparative proteomic analysis of two distinct stem-cell populations from human amniotic fluid

Abstract

Human amniotic fluid (AF) contains a variety of stem cells of embryonic and extra-embryonic origins. We characterized two distinct types of stem cells isolated from residual AF material derived from prenatal diagnostic amniocentesis. The two types of cells differed in their morphology and growth kinetics, showing fast (fast human amniotic stem cells; fHASCs) or slow (slow human amniotic stem cells; sHASCs) population-doubling times. Both fHASCs and sHASCs expressed pluripotent stem-cell markers, yet unlike sHASCs, clonogenic fHASCs would generate embryoid bodies and maintain their original phenotype during prolonged in vitro passaging. fHASCs – but not sHASCs – expressed the KLF4, SSEA-4 and CD117 markers. Differential proteomic analysis allowed us to identify the protein patterns specific for either cell type as potentially contributing to their distinct phenotypes. We found thirty-six proteins that were differentially expressed by the two cell types, and those proteins were classified according to their biological and molecular functions. Bioinformatic cluster analysis revealed differential occurrence of cytoskeletal proteins, such as vimentin, F-actin-binding protein, and chloride intracellular channel protein 1. Selected proteins differentially expressed by fHASCs and sHASCs were further characterized by Western blot analysis and confocal microscopy.

Graphical abstract: Comparative proteomic analysis of two distinct stem-cell populations from human amniotic fluid

  • This article is part of the themed collection: Proteomics

Supplementary files

Article information

Article type
Paper
Submitted
09 Jan 2015
Accepted
13 Mar 2015
First published
16 Mar 2015

Mol. BioSyst., 2015,11, 1622-1632

Comparative proteomic analysis of two distinct stem-cell populations from human amniotic fluid

R. Romani, F. Fallarino, I. Pirisinu, M. Calvitti, A. Caselli, T. Fiaschi, T. Gamberi, D. Matino, V. N. Talesa, E. Donti, P. Puccetti, A. Modesti and F. Magherini, Mol. BioSyst., 2015, 11, 1622 DOI: 10.1039/C5MB00018A

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