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Mesenchyme-derived vertebrate lonesome kinase controls lung organogenesis by altering the matrisome


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Date

2023-04

Publication Type

Journal Article

ETH Bibliography

yes

Citations

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Data

Abstract

Vertebrate lonesome kinase (VLK) is the only known secreted tyrosine kinase and responsible for the phosphorylation of a broad range of secretory pathway-resident and extracellular matrix proteins. However, its cell-type specific functions in vivo are still largely unknown. Therefore, we generated mice lacking the VLK gene (protein kinase domain containing, cytoplasmic (Pkdcc)) in mesenchymal cells. Most of the homozygous mice died shortly after birth, most likely as a consequence of their lung abnormalities and consequent respiratory failure. E18.5 embryonic lungs showed a reduction of alveolar type II cells, smaller bronchi, and an increased lung tissue density. Global mass spectrometry-based quantitative proteomics identified 97 proteins with significantly and at least 1.5-fold differential abundance between genotypes. Twenty-five of these had been assigned to the extracellular region and 15 to the mouse matrisome. Specifically, fibromodulin and matrilin-4, which are involved in extracellular matrix organization, were significantly more abundant in lungs from Pkdcc knockout embryos. These results support a role for mesenchyme-derived VLK in lung development through regulation of matrix dynamics and the resulting modulation of alveolar epithelial cell differentiation.

Publication status

published

Editor

Book title

Volume

80 (4)

Pages / Article No.

89

Publisher

Springer

Event

Edition / version

Methods

Software

Geographic location

Date collected

Date created

Subject

Pkdcc; Lung organogenesis; Collagen; Skull; Proteomics

Organisational unit

03520 - Werner, Sabine / Werner, Sabine check_circle

Notes

Funding

ETH-25 17-1 - Role of extracellular tyrosine phosphorylation in collagen processing and wound healing (ETHZ)

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