Science and Research

Death-associated protein kinase 1 prevents hypoxia-induced metabolic shift and pulmonary arterial smooth muscle cell proliferation in PAH

Pulmonary hypertension (PH) is a general term used to describe high blood pressure in the lungs from any cause. Pulmonary arterial hypertension (PAH) is a progressive, and fatal disease that causes the walls of the pulmonary arteries to tighten and stiffen. One of the major characteristics of PAH is the hyperproliferation and resistance to apoptosis of vascular cells, which trigger excessive pulmonary vascular remodeling and vasoconstriction. The death-associated protein DAP-kinase (DAPK) is a tumor suppressor and Ser/Thr protein kinase, which was previously shown to regulate the hypoxia inducible factor (HIF)-1

  • Seidel, L. M.
  • Thudium, J.
  • Smith, C.
  • Sapehia, V.
  • Sommer, N.
  • Wujak, M.
  • Weissmann, N.
  • Seeger, W.
  • Schermuly, R. T.
  • Novoyatleva, T.

Keywords

  • Dapk1
  • Hif
  • Metabolic shift
  • Mitochondrial respiration
  • Proliferation
  • Pulmonary artery smooth muscle cells
Publication details
DOI: 10.1016/j.cellsig.2024.111527
Journal: Cell Signal
Pages: 111527 
Work Type: Original
Location: UGMLC
Disease Area: PH
Partner / Member: JLU, MPI-BN
Access-Number: 39622428

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