Human Lung Spheroids as In Vitro Niches of Lung Progenitor Cells with Distinctive Paracrine and Plasticity Properties. (22nd September 2016)

• Record Type: Journal Article
• Authors: Chimenti, Isotta; Pagano, Francesca; Angelini, Francesco; Siciliano, Camilla; Mangino, Giorgio; Picchio, Vittorio; De Falco, Elena; Peruzzi, Mariangela; Carnevale, Roberto; Ibrahim, Mohsen; Biondi-Zoccai, Giuseppe; Messina, Elisa; Frati, Giacomo
• Is Part Of: Stem cells translational medicine. Volume 6:Number 3(2017)
• Page Start: 767
• Page End: 777
• Publication Date: 2016-09-22
• Subjects: Lung stem cells -- Pneumospheres -- Three-dimensional culture -- Stem cell niche -- Epithelial-to-mesenchymal transition; Stem cells -- Periodicals; Regenerative medicine -- Periodicals; Periodicals; 616.0277405
• DOI: 10.5966/sctm.2015-0374
• Languages: English
• ISSNs: 2157-6564

Abstract

Abstract: Basic and translational research on lung biology has discovered multiple progenitor cell types, specialized or facultative, responsible for turnover, renewal, and repair. Isolation of populations of resident lung progenitor cells (LPCs) has been described by multiple protocols, and some have been successfully applied to healthy human lung tissue. We aimed at understanding how different cell culture conditions may affect, in vitro, the phenotype of LPCs to create an ideal niche-like microenvironment. The influence of different substrates (i.e., fibronectin, gelatin, laminin) and the impact of a three-dimensional/two-dimensional (3D/2D) culture switch on the biology of LPCs isolated as lung spheroids (LSs) from normal adult human lung biopsy specimens were investigated. We applied a spheroid culture system as the selective/inductive step for progenitor cell culture, as described in many biological systems. The data showed a niche-like proepithelial microenvironment inside the LS, highly sensitive to the 3D culture system and significantly affecting the phenotype of adult LPCs more than culture substrate. LSs favor epithelial phenotypes and LPC maintenance and contain cells more responsive to specific commitment stimuli than 2D monolayer cultures, while secreting a distinctive set of paracrine factors. We have shown for the first time, to our knowledge, how culture as 3D LSs can affect LPC epithelial phenotype and produce strong paracrine signals with a distinctive secretomic profile compared with 2D monolayer conditions. These findings suggest novel approaches to maintain ex vivo LPCs for basic and translational studies.