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pulmonary artery smooth muscle cells (smcs)  (Lonza)


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    Lonza pulmonary artery smooth muscle cells (smcs)
    Pulmonary Artery Smooth Muscle Cells (Smcs), supplied by Lonza, 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/pulmonary+artery+smc/pulmonary+artery+smooth+muscle+cells/pmc11110101-112-3-8
    Average 90 stars, based on 1 article reviews
    pulmonary artery smooth muscle cells (smcs) - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Hypoxia-induced endothelial CX3CL1 triggers lung smooth muscle cell phenotypic switching and proliferative expansion
    Article Snippet: Human pulmonary MVEC, pulmonary artery endothelial cells, and pulmonary artery SMC were purchased from Lonza and propagated in monolayer cultures as described by Zhang et al. ( 59 , 62 ).



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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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    PM 2.5 and PM 2.5-10 induced cell migration in HPASMCs, <t>MPASMCs,</t> 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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    Image Search Results


    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

    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: Mouse pulmonary artery SMCs (MPASMCs) were purchased from Cell Biologics Inc. (Chicago, IL, USA; cat# C57-6083) and cultured in SMC medium (Cell Biologics Inc., Chicago, IL, USA; cat# M2268).

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