Human Second Trimester Amniotic Fluid Cells are Able to Create Embryoid Body-Like Structures in Vitro and to Show Typical Expression Profiles of Embryonic and Primordial Germ Cells

Author:

Antonucci Ivana12,Di Pietro Roberta13,Alfonsi Melissa4,Centurione Maria Antonietta13,Centurione Lucia13,Sancilio Silvia4,Pelagatti Francesca1,D'amico Maria Angela3,Di Baldassarre Angela4,Piattelli Adriano4,Tetè Stefano25,Palka Giandomenico5,Borlongan Cesar V.6,Stuppia Liborio12

Affiliation:

1. Laboratory of Molecular Genetics, Department of Psychological, Humanities and Territorial Sciences, School of Medicine and Health Sciences, G. d'Annunzio University Chieti-Pescara, Chieti, Italy

2. Stem Tech Group, Center for Aging Studies (CESI), “G. d'Annunzio” University, Chieti-Pescara, Italy

3. Department of Medicine and Aging Sciences, School of Medicine and Health Sciences

4. Pharmacy Department, “G. d'Annunzio” University, Chieti-Pescara, Italy

5. Department of Clinical, Oral and Biotechnological Sciences, School of Medicine and Health Sciences, “G. d'Annunzio” University, Chieti-Pescara, Italy

6. Department of Neurosurgery and Brain Repair, Center of Excellence for Aging and Brain Repair, University of South Florida Morsani College of Medicine, Tampa, FL, USA

Abstract

Human amniotic fluid-derived stem cells (AFSCs) represent a novel class of broadly multipotent stem cells sharing characteristics of both embryonic and adult stem cells. However, both the origin of these cells and their actual properties in terms of pluripotent differentiation potential are still debated. In order to verify the presence of features of pluripotency in human second trimester AFSCs, we have investigated the ability of these cells to form in vitro three-dimensional aggregates, known as embryoid bodies (EBs), and to express specific genes of embryonic stem cells (ESCs) and primordial germ cells (PGCs). EBs were obtained after 5 days of AFSC culture in suspension and showed positivity for alkaline phosphatase (AP) staining and for specific markers of pluripotency (OCT4 and SOX2). Moreover, EB-derived cells showed the expression of specific transcripts of the three germ layers. RT-PCR analysis, carried out at different culture times (second, third, fourth, fifth, and eighth passages), revealed the presence of specific markers of ESCs (such as FGF4 and DAPPA4), as well as of markers typical of PGCs and, in particular, genes involved in early stages of germ cell development (Fragilis, Stella, Vasa, c-Kit, Rnf17). Finally, the expression of genes related to the control of DNA methylation (DNMT3A, DNMT3b1, DNMT1, DNMT3L, MBD1, MBD2, MBD3, MDB4, MeCP2), as well as the lack of inactivation of the X-chromosome in female samples, was also demonstrated. Taken together, these data provide further evidence for the presence of common features among human AFSCs, PGCs, and ESCs.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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