FFC#5/2017

Dissecting the potency of human Mesoangioblasts to differentiate into CFTR-expressing epithelial cells: a step forward to an innovative cell-based therapy for Cystic Fibrosis disease

AREA 1 Therapies to correct the underlying defect

FFC#5/2017

Dissecting the potency of human Mesoangioblasts to differentiate into CFTR-expressing epithelial cells: a step forward to an innovative cell-based therapy for Cystic Fibrosis disease
€ 0 still needed
0%
€ 30.000 goal

pRINCIPAL INVESTIGATOR

Graziella Messina (Dipartimento di Bioscienze, Università degli Studi di Milano)

Researchers

7

Category

AREA 1 Therapies to correct the underlying defect

Duration

1 year

Goal

€ 30.000

Funds raised

€ 30.000

Objectives

In previous FFC projects the researchers show that mouse Mesoangioblasts (mMABs), vessel-associated adult progenitor cells, when systemically transplanted in CF mouse models, are able to engraft over time the epithelium of airways and intestine, contributing to the epithelial tissue and rescuing the CFTR function (FFC#5/2013, FFC#6/2015). Now their aim is to investigate if human MABs (hMABS) have the same properties. Different populations of human MABs (hMABs) will be tested for the expression of CFTR. Moreover, hMABS will be co-cultured with human bronchiolar epithelial cells from healthy control or CF patients bearing severe mutations of CFTR (F508del, N1303K). In this coculture system, hMABs ability to differentiate into epithelium and to express a functional CFTR (by Ussing chamber) will be tested. The project may help to establish new scientific bases for the application of cell-based therapies to CF.

WHO ADOPTED THE PROJECT

Delegazione FFC di Roma Pomezia per Sara, Andrea e Michol

€ 30.000

Delegazione FFC di Vittoria, Ragusa e Siracusa

€ 19.000

Delegazione FFC di Catania Mascalucia

€ 19.000

OTHER PROJECTS

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GMRF#1/2026

Exploring the role of PKD1 in promoting CFTR stability and function at the cell surface

FFC#1/2026

Mapping proteins regulating CFTR mRNA stability to identify new therapeutic targets for nonsense mutations

FFC#2/2026

Evaluating the potential of phosphodiesterase inhibitors to enhance the efficacy of CFTR modulators and support personalized therapeutic approaches