Recent advances in our understanding of the mechanisms of late lung development and bronchopulmonary dysplasia

DE Surate Solaligue… - … of Physiology-Lung …, 2017 - journals.physiology.org
The objective of lung development is to generate an organ of gas exchange that provides
both a thin gas diffusion barrier and a large gas diffusion surface area, which concomitantly …

PPARγ links BMP2 and TGFβ1 pathways in vascular smooth muscle cells, regulating cell proliferation and glucose metabolism

L Calvier, P Chouvarine, E Legchenko, N Hoffmann… - Cell metabolism, 2017 - cell.com
BMP2 and TGFβ1 are functional antagonists of pathological remodeling in the arteries,
heart, and lung; however, the mechanisms in VSMCs, and their disturbance in pulmonary …

Phenotypes in pulmonary hypertension

J Weatherald, AR Hemnes, BA Maron… - European …, 2024 - publications.ersnet.org
The clinical classification of pulmonary hypertension (PH) has guided diagnosis and
treatment of patients with PH for several decades. Discoveries relating to underlying …

Pulmonary hypertension secondary to pulmonary fibrosis: clinical data, histopathology and molecular insights

G Ruffenach, J Hong, M Vaillancourt, L Medzikovic… - Respiratory …, 2020 - Springer
Pulmonary hypertension (PH) develo** secondarily in pulmonary fibrosis (PF) patients
(PF-PH) is a frequent co-morbidity. The high prevalence of PH in PF patients is very …

Emerging mechanisms of pulmonary vasoconstriction in SARS-CoV-2-induced acute respiratory distress syndrome (ARDS) and potential therapeutic targets

H Karmouty-Quintana, RA Thandavarayan… - International journal of …, 2020 - mdpi.com
The 1918 influenza killed approximately 50 million people in a few short years, and now, the
world is facing another pandemic. In December 2019, a novel coronavirus named severe …

[HTML][HTML] Lipid nanoparticle-mediated mRNA delivery in lung fibrosis

M Massaro, S Wu, G Baudo, H Liu, S Collum… - European Journal of …, 2023 - Elsevier
Abstract mRNA delivery enables the specific synthesis of proteins with therapeutic potential,
representing a powerful strategy in diseases lacking efficacious pharmacotherapies …

Impairment of the NKT–STAT1–CXCL9 axis contributes to vessel fibrosis in pulmonary hypertension caused by lung fibrosis

K Jandl, LM Marsh, AC Mutgan, S Crnkovic… - American Journal of …, 2022 - atsjournals.org
Rationale: Pulmonary hypertension (PH) is a common, severe comorbidity in interstitial lung
diseases such as pulmonary fibrosis (PF), and it has limited treatment options. Excessive …

Consequences of BMPR2 deficiency in the pulmonary vasculature and beyond: contributions to pulmonary arterial hypertension

A Andruska, E Spiekerkoetter - International journal of molecular sciences, 2018 - mdpi.com
Since its association with familial pulmonary arterial hypertension (PAH) in 2000, Bone
Morphogenetic Protein Receptor II (BMPR2) and its related signaling pathway have become …

BMP type II receptor as a therapeutic target in pulmonary arterial hypertension

M Orriols, MC Gomez-Puerto, P Ten Dijke - Cellular and Molecular Life …, 2017 - Springer
Pulmonary arterial hypertension (PAH) is a chronic disease characterized by a progressive
elevation in mean pulmonary arterial pressure. This occurs due to abnormal remodeling of …

The role of circular RNAs in pulmonary hypertension

MK Ali, K Schimmel, L Zhao, CK Chen… - European …, 2022 - Eur Respiratory Soc
Circular RNAs (circRNAs) are endogenous, covalently circularised, non-protein-coding
RNAs generated from back-splicing. Most circRNAs are very stable, highly conserved, and …