Plasticity of Hopx+ type I alveolar cells to regenerate type II cells in the lung

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作者
Rajan Jain
Christina E. Barkauskas
Norifumi Takeda
Emily J. Bowie
Haig Aghajanian
Qiaohong Wang
Arun Padmanabhan
Lauren J. Manderfield
Mudit Gupta
Deqiang Li
Li Li
Chinmay M. Trivedi
Brigid L. M. Hogan
Jonathan A. Epstein
机构
[1] Penn Cardiovascular Institute,Department of Cell and Developmental Biology
[2] Institute of Regenerative Medicine,Division of Pulmonary, Department of Medicine
[3] Perelman School of Medicine at the University of Pennsylvania,Department of Cell Biology
[4] Allergy,undefined
[5] and Critical Care Medicine,undefined
[6] Duke Medicine,undefined
[7] Duke Medicine,undefined
[8] Present address: Department of Cardiovascular Medicine,undefined
[9] The University of Tokyo Hospital,undefined
[10] 7-3-1 Hongo,undefined
[11] Bunkyo,undefined
[12] Tokyo 113-8655,undefined
[13] Japan.,undefined
[14] Present address: Massachusetts General Hospital,undefined
[15] 55 Fruit Street,undefined
[16] Boston,undefined
[17] Massachusetts 02114,undefined
[18] USA.,undefined
[19] Present address: University of Massachusetts Medical School,undefined
[20] 368 Plantation Street,undefined
[21] Worcester,undefined
[22] Massachusetts 01605,undefined
[23] USA.,undefined
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摘要
The plasticity of differentiated cells in adult tissues undergoing repair is an area of intense research. Pulmonary alveolar type II cells produce surfactant and function as progenitors in the adult, demonstrating both self-renewal and differentiation into gas exchanging type I cells. In vivo, type I cells are thought to be terminally differentiated and their ability to give rise to alternate lineages has not been reported. Here we show that Hopx becomes restricted to type I cells during development. However, unexpectedly, lineage-labelled Hopx+ cells both proliferate and generate type II cells during adult alveolar regrowth following partial pneumonectomy. In clonal 3D culture, single Hopx+ type I cells generate organoids composed of type I and type II cells, a process modulated by TGFβ signalling. These findings demonstrate unanticipated plasticity of type I cells and a bidirectional lineage relationship between distinct differentiated alveolar epithelial cell types in vivo and in single-cell culture.
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