the-production-pluripotent-stem-cells-from-mouse-amniotic-fluid-cells

The Production of Pluripotent Stem Cells from Mouse Amniotic Fluid Cells Using a Transposon System

Induced pluripotent stem (iPS) cells are generated from mouse and human somatic cells by forced expression of defined transcription factors using ...

Fondazione Istituto di Ricerca Pediatrica Citta della Speranza

Mutations in the survival of motor neuron gene (SMN1) are responsible for spinal muscular atrophy, a fatal neuromuscular disorder. Mice carrying a homozygous deletion of Smn exon 7 directed to skeletal muscle (HSA-Cre, Smn(F7/F7) mice) present clinical features of human muscular dystrophies for which new therapeutic approaches are highly warranted. Herein we demonstrate that tail vein transplantation of mouse amniotic fluid stem (AFS) cells enhances the muscle strength and improves the survival rate of the affected animals. Second, after cardiotoxin injury of the Tibialis Anterior, only AFS-transplanted mice efficiently regenerate. Most importantly, secondary transplants of satellite cells (SCs) derived from treated mice show that AFS cells integrate into the muscle stem cell compartment and have long-term muscle regeneration capacity indistinguishable from that of wild-type-derived SC. This is the first study demonstrating the functional and stable integration of AFS cells into the skeletal muscle, highlighting their value as cell source for the treatment of muscular dystrophies.

Amniotic fluid stem cells restore the muscle cell niche in a HSA-Cre, Smn(F7/F7) mouse model.

In the last few years recent evidence has revealed that inside an apparently homogeneous cell population there indeed appears to be heterogeneity. This is particularly true for embryonic stem (ES) cells where markers of pluripotency are dynamically expressed within the single cells. In this work we have designed and tested a new set of primers for multiplex PCR detection of pluripotency markers expression, and have applied it to perform single cell analysis in murine ES cells cultured on three different substrates that could play an important role in controlling cell behaviour and fate: i) mouse embryonic fibroblast (MEF) feeder layer, as the standard method for ES cells culture; ii) Matrigel coating; iii) micropatterned hydrogel.

Single cell PCR analysis of murine embryonic stem cells cultured on different substrates highlights heterogeneous expression of stem cell markers.

Endothelial dysfunction is found in different pathologies such as diabetes and renal and heart diseases, representing one of the major health problems. The reduced vasodilation of impaired endothelium starts a prothrombotic state associated with irregular blood flow. We aimed to explore the potential of amniotic fluid stem (AFS) cells as a source for regenerative medicine in this field; for the first time, we focused on third-trimester amniotic fluid AFS cells and compared them with the already-described AFS cells from the second trimester.

Enrica Bertin

Stem Cell and Regenerative Medicine Laboratory

Fondazione Istituto di Ricerca Pediatrica Citta della Speranza

The Production of Pluripotent Stem Cells from Mouse Amniotic Fluid Cells Using a Transposon System

Enrica Bertin

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Fondazione Istituto di Ricerca Pediatrica Citta della Speranza

The Production of Pluripotent Stem Cells from Mouse Amniotic Fluid Cells Using a Transposon System

Stem Cell and Regenerative Medicine Laboratory