4.6 Article

Upregulation of mechanosensitive channel Piezo1 involved in high shear stress-induced pulmonary hypertension

Journal

THROMBOSIS RESEARCH
Volume 218, Issue -, Pages 52-63

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.thromres.2022.08.006

Keywords

Piezo1; Shear stress; Pulmonary hypertension; Smooth muscle cell; Endothelial cell

Funding

  1. National Natural Science Foundation of China [82120108001, 81970057, 82170065, 82170069, 81960013]
  2. National Key Research and Development Pro-gram of China [2018YFC1311900]
  3. Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01S155]
  4. Guangdong Basic and Applied Basic Research Foun-dation [2021A1515010767, 2019A1515010615]
  5. Guangzhou Basic Research Program Municipal School (Hospital) Joint Funded Founda-tion and Application Basic Research Project [ZNSA-2020003]
  6. Inde-pendent Project of State Key Laboratory of Respiratory Disease [SKLRD-Z-202219, SKLRD-Z-202207, SKLRD-Z-202101]
  7. Independent Project of the State Key Laboratory of Respiratory Disease, Guangdong-Hong Kong-Macao Joint Laboratory of Respiratory Infectious Disease [GHMJLRID-Z-202110, GHMJLRID-Z-202120, 202201-101]
  8. Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences [2019PT350001]
  9. National Natural Sci-ence Foundation of China [202201010152]
  10. Guangzhou Science and Technology Plan [81960013]
  11. Open Project of The Sixth Affiliated Hospital of Guangzhou Medical University
  12. [202201-309]

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Piezo1 plays an important role in pulmonary vascular remodeling during the development of pulmonary hypertension (PH). Upregulation of Piezo1 is associated with inhibited pulmonary vascular contraction and relaxation, and is related to different cell signaling pathways in pulmonary arterial smooth muscle cells (PASMCs) and endothelial cells (ECs).
Introduction: Piezo1 is an important mechanosensitive channel implicated in vascular remodeling. However, the role of Piezo1 in different types of vascular cells during the development of pulmonary hypertension (PH) induced by high shear stress is largely unknown.Materials and methods: We used a rat PH model established by left pulmonary artery ligation (LPAL, for 2-5 weeks), which mimics the high flow and hemodynamic stress, to study Piezo1 contribution to pulmonary vascular remodeling.Results: Right ventricular systolic pressure (RVSP), a surrogate measure for pulmonary arterial systolic pressure, and right ventricular wall thickness, a measure for right ventricular hypertrophy, were significantly increased in LPAL rats compared with Sham-control (SHAM) rats. Rats in LPAL-5w groups developed remarkable pulmonary vascular remodeling, while phenylephrine-induced contraction and acetylcholine-induced relaxation were both significantly inhibited in these rats. Upregulation of Piezo1, in association with increase in cytosolic Ca2+ con-centration ([Ca2+]cyt), was observed in pulmonary arterial smooth muscle cells (PASMCs) from LPAL-2w and LPAL-5w rats in comparison to the SHAM controls. Piezo1 upregulation in PASMCs from LPAL rats was directly related to Yes-associated protein (YAP)/ TEA domain transcription factor 4 (TEAD4). Piezo1 expression was also upregulated in the whole-lung tissue of LPAL rats. The endothelial upregulation of Piezo1 was related to tran-scriptional regulation by RELA (p65) and lung inflammation.Conclusion: The upregulation of Piezo1 in both PASMCs and ECs coordinates with each other via different cell signaling pathways to cause pulmonary vascular remodeling in LPAL-PH rats, providing novel insights into the cell-type specific pathogenic roles of Piezo1 in shear stress-associated experimental PH.

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