Publications by authors named "Anas Rabata"

Article Synopsis
  • Idiopathic pulmonary fibrosis (IPF) is linked to aging and is characterized by damage to lung epithelial cells, particularly alveolar type II cells (AEC2s) that play a crucial role in lung repair.
  • Research showed downregulation of lipid metabolism-related genes in AEC2s from both IPF patients and older mice with lung injury, which worsens with age and impairs recovery.
  • Targeting lipid metabolism in AEC2s through supplementation or activation of certain receptors can enhance their regenerative capabilities, suggesting a potential therapeutic avenue for treating IPF.
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Article Synopsis
  • Progressive pulmonary fibrosis is caused by defective tissue repair, leading to increased fibroblast activity and extracellular matrix buildup in lungs.
  • Recent studies using single-cell RNA sequencing have identified various fibroblast subtypes in both mice and humans, but their specific roles in lung fibrosis remain unclear.
  • The study successfully identified and isolated distinct fibroblast subtypes, revealing that lipofibroblasts and Ebf1 fibroblasts play significant roles in matrix production and invasive behavior, offering potential targets for new therapies in lung fibrosis.
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Background: The progenitors to lung airway epithelium that are capable of long-term propagation may represent an attractive source of cells for cell-based therapies, disease modeling, toxicity testing, and others. Principally, there are two main options for obtaining lung epithelial progenitors: (i) direct isolation of endogenous progenitors from human lungs and (ii) in vitro differentiation from some other cell type. The prime candidates for the second approach are pluripotent stem cells, which may provide autologous and/or allogeneic cell resource in clinically relevant quality and quantity.

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FGF signaling plays an essential role in lung development, homeostasis, and regeneration. We employed mouse 3D cell culture models and imaging to study the role of FGF ligands and the interplay of FGF signaling with epithelial growth factor (EGF) and WNT signaling pathways in lung epithelial morphogenesis and differentiation. In non-adherent conditions, FGF signaling promoted formation of lungospheres from lung epithelial stem/progenitor cells (LSPCs).

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Fibroblast growth factor 2 (FGF2) plays important roles in tissue development and repair. Using heparan sulfates (HS)/heparin as a cofactor, FGF2 binds to FGF receptor (FGFR) and induces downstream signaling pathways, such as ERK pathway, that regulate cellular behavior. In most cell lines, FGF2 signaling displays biphasic dose-response profile, reaching maximal response to intermediate concentrations, but weak response to high levels of FGF2.

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Extracellular matrix (ECM) is an essential component of the tissue microenvironment, actively shaping cellular behavior. In vitro culture systems are often poor in ECM constituents, thus not allowing for naturally occurring cell-ECM interactions. This study reports on a straightforward and efficient method for the generation of ECM scaffolds from lung tissue and its subsequent in vitro application using primary lung cells.

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Lung epithelium contains distinctive subpopulations of lung stem/progenitor cells (LSPCs) that are essential for lung epithelial maintenance and repair in vivo. Hence, LSPCs are in the center of interest of lung biology due to their promising therapeutic applications. To reach this goal, proper characterization of LSPCs, understanding of their proliferation and differentiation potentials and elucidation of mechanisms that control them are necessary.

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