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Ludwig Boltzmann Gesellschaft human pulmonary artery smcs
Human Pulmonary Artery Smcs, supplied by Ludwig Boltzmann Gesellschaft, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+pulmonary+artery+smcs/human+pulmonary+artery+smcs/pm32692930-54-0-16
Average 90 stars, based on 1 article reviews
human pulmonary artery smcs - by Bioz Stars, 2026-10
90/100 stars

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Article Title: TWIST1 Drives Smooth Muscle Cell Proliferation in Pulmonary Hypertension via Loss of GATA-6 and BMPR2
Article Snippet: Rationale: The basic helix-loop-helix transcription factor TWIST1 controls cell proliferation and differentiation in tissue development and disease processes.. Recently, endothelial TWIST1 has been linked to pulmonary hypertension (PH) and endothelial-to-mesenchymal transition, yet the role of TWIST1 in smooth muscle cells remains so far unclear.. Objective: To define the role of TWIST1 in smooth muscle cells (SMC) in the pathogenesis of PH.

Article Title: TWIST1 Drives Smooth Muscle Cell Proliferation in Pulmonary Hypertension via Loss of GATA-6 and BMPR2.
Article Snippet: Human pulmonary artery SMCs from patients with idiopathic PAH and donor controls were obtained from the Ludwig Boltzmann Institute for Lung Vascular Research in Graz, Austria.



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PM 2.5 and PM 2.5-10 induced cell migration in <t>HPASMCs,</t> MPASMCs, and MVSMCs. HPASMCs were treated with d 2 H 2 O or 25 μg/mL PM 2.5 or PM 2.5-10 for 48 h. Migration abilities of HPASMCs, MPASMCs, and MVSMCs were measured, quantified and shown as ( A , B , D , E , G , H ). The relative levels of SMA mRNA for HPASMCs, MPASMCs, and MVSMCs were determined using a real-time PCR assay, and shown as ( C , F , I ). ( J ) MVSMCs were stained with Alexa Fluor 546-Phalloidin.(red) to identify lamellipodia (white arrows). The results are presented as the mean ± SD for three or four independent experiments. * p < 0.05, compared with d 2 H 2 O-treated cells. Con: d 2 H 2 O treatment as control.
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Ludwig Boltzmann Gesellschaft human pulmonary artery smcs
PM 2.5 and PM 2.5-10 induced cell migration in <t>HPASMCs,</t> MPASMCs, and MVSMCs. HPASMCs were treated with d 2 H 2 O or 25 μg/mL PM 2.5 or PM 2.5-10 for 48 h. Migration abilities of HPASMCs, MPASMCs, and MVSMCs were measured, quantified and shown as ( A , B , D , E , G , H ). The relative levels of SMA mRNA for HPASMCs, MPASMCs, and MVSMCs were determined using a real-time PCR assay, and shown as ( C , F , I ). ( J ) MVSMCs were stained with Alexa Fluor 546-Phalloidin.(red) to identify lamellipodia (white arrows). The results are presented as the mean ± SD for three or four independent experiments. * p < 0.05, compared with d 2 H 2 O-treated cells. Con: d 2 H 2 O treatment as control.
Human Pulmonary Artery Smcs, supplied by Ludwig Boltzmann Gesellschaft, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+pulmonary+artery+smcs/human+pulmonary+artery+smcs/pm32692930-54-0-16
Average 90 stars, based on 1 article reviews
human pulmonary artery smcs - by Bioz Stars, 2026-10
90/100 stars
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PM 2.5 and PM 2.5-10 induced cell migration in HPASMCs, MPASMCs, and MVSMCs. HPASMCs were treated with d 2 H 2 O or 25 μg/mL PM 2.5 or PM 2.5-10 for 48 h. Migration abilities of HPASMCs, MPASMCs, and MVSMCs were measured, quantified and shown as ( A , B , D , E , G , H ). The relative levels of SMA mRNA for HPASMCs, MPASMCs, and MVSMCs were determined using a real-time PCR assay, and shown as ( C , F , I ). ( J ) MVSMCs were stained with Alexa Fluor 546-Phalloidin.(red) to identify lamellipodia (white arrows). The results are presented as the mean ± SD for three or four independent experiments. * p < 0.05, compared with d 2 H 2 O-treated cells. Con: d 2 H 2 O treatment as control.

Journal: Antioxidants

Article Title: Ambient Particulate Matter Induces Vascular Smooth Muscle Cell Phenotypic Changes via NOX1/ROS/NF-κB Dependent and Independent Pathways: Protective Effects of Polyphenols

doi: 10.3390/antiox10050782

Figure Lengend Snippet: PM 2.5 and PM 2.5-10 induced cell migration in HPASMCs, MPASMCs, and MVSMCs. HPASMCs were treated with d 2 H 2 O or 25 μg/mL PM 2.5 or PM 2.5-10 for 48 h. Migration abilities of HPASMCs, MPASMCs, and MVSMCs were measured, quantified and shown as ( A , B , D , E , G , H ). The relative levels of SMA mRNA for HPASMCs, MPASMCs, and MVSMCs were determined using a real-time PCR assay, and shown as ( C , F , I ). ( J ) MVSMCs were stained with Alexa Fluor 546-Phalloidin.(red) to identify lamellipodia (white arrows). The results are presented as the mean ± SD for three or four independent experiments. * p < 0.05, compared with d 2 H 2 O-treated cells. Con: d 2 H 2 O treatment as control.

Article Snippet: Human pulmonary artery SMCs (HPASMCs) were purchased from Lonza (Walkersville, MD, USA) (Cat# CC2581) and cultured in SMC medium (Lonza, Walkersville, MD, USA; cat# CC3182).

Techniques: Migration, Real-time Polymerase Chain Reaction, Staining, Control