The ZIP8/SIRT1 axis regulates alveolar progenitor cell renewal in aging and idiopathic pulmonary fibrosis
Type 2 alveolar epithelial cells (AEC2s) function as progenitor cells in the lung. We have shown previously that failure of AEC2 regeneration results in progressive lung fibrosis in mice and is a cardinal feature of idiopathic pulmonary fibrosis (IPF). In this study, we identified deficiency of a specific zinc transporter, SLC39A8 (ZIP8), in AEC2s from both IPF lungs and lungs of old mice. Loss of ZIP8 expression was associated with impaired renewal capacity of AEC2s and enhanced lung fibrosis. ZIP8 regulation of AEC2 progenitor function was dependent on SIRT1. Replenishment with exogenous zinc and SIRT1 activation promoted self-renewal and differentiation of AEC2s from lung tissues of IPF patients and old mice.
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Atlas

Analysis Portals
Project Label
Liang_Human_Mouse_IPFlung_10xSpecies
Sample Type
specimens
Anatomical Entity
lung
Organ Part
Unspecified
Selected Cell Types
epithelial cell
Disease Status (Specimen)
pulmonary fibrosis
Disease Status (Donor)
Development Stage
Library Construction Method
10x 3' v2
Nucleic Acid Source
single cell
Paired End
falseAnalysis Protocol
analysis_alignment_human, analysis_alignment_mouseFile Format
Cell Count Estimate
26.1kDonor Count
38