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Cellules musculaires lisses de l'artère pulmonaire humaine (HPASMC)
Tissu
Lung (pulmonary artery
Maladie
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Site métastatique
Not applicable (normal, non-tumorigenic primary cell)
Synonymes
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Documents

Cellules musculaires lisses de l'artère pulmonaire humaine (HPASMC)

Primary cell · Référence du produit 300706

Muscle lisse vasculaire pulmonaire destiné à la recherche sur l'HTAP

€1,490.00hors taxes et frais de port

Personnalisation / Recommandations

Fabriqué sur commande
1

01Description

02Informations générales

Description

Primary Human Pulmonary Artery Smooth Muscle Cells (HPASMC) are isolated from the pulmonary artery. They are a key model for pulmonary arterial hypertension, including hypoxia-driven proliferation and vascular remodeling.

Hypoxia drives the proliferation of HPASMC, and PDGF-BB shifts them toward a synthetic, migratory phenotype, reproducing key features of pulmonary vascular remodeling. Because the balance of BMP and TGF-β signaling is central to pulmonary arterial hypertension, the cells are also used to study BMPR2-related mechanisms.

Tissu
Lung (pulmonary artery
Maladie
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Site métastatique
Not applicable (normal, non-tumorigenic primary cell)
Applications
Pulmonary arterial hypertension: BMP/TGF-β balance, proliferation and migration; Hypoxia-induced proliferation, PPARγ and microRNA-21; Long non-coding RNA regulation of migration in pulmonary arterial hypertension; Functional testing of BMPR2 promoter variants in reporter assays; PDGF-BB-induced phenotype switching and metabolomics; Endothelin-1 signaling and proteomics of BMPR2-mutant cells
Synonymes
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Donateur

Âge du donneur
Lot-specific (see CoA)
Origine ethnique
Lot-specific (see CoA)

04Classification

Organisme
Humain
Sexe
Spécifique au lot
Propriétés de croissance
Adepte
Statut OGM
Sans OGM
Informations détaillées sur le statut OGM
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Niveau de biosécurité
1

05Caractéristiques

Morphologie
Spindle-shaped (smooth muscle)
Type de cellule
Primary smooth muscle cells
Tumorigène
No
Temps de doublement
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Manipulation et culture

Milieu de culture
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Atmosphère d'incubation

37°C, 5% CO2, saturated humidity.

Compléments alimentaires
Supplement as specified in the AddexBio SMC supplement kit (refer to specification sheet). For cryopreservation: complete culture medium + 5% (v/v) DMSO.
Réactif de dissociation
Subculture reagents as recommended on the certificate of analysis
Repiquage

Subculture the cells at about 75 % confluence. Denser cultures undergo irreversible contact inhibition and stop proliferating. Use the subculture reagents recommended on the certificate of analysis.

Rapport de fractionnement
1 to 3
Densité de semis
More than 4,000 cells/cm²
Renouvellement des fluides
24 hours after seeding, then every 48 to 72 hours
Récupération après le dégel

Post-thaw viability ≥ 70 % viable cells. More than 80 % confluence within the expected recovery period.

Décongélation et mise en culture
  1. Thaw the cryovial quickly in a 37 °C water bath, swirling gently. Just before the last ice has melted, move the vial to a laminar flow hood and decontaminate its outer surface.

  2. Transfer the cell suspension into a 15 ml centrifuge tube, add 10 ml of Smooth Muscle Cell Growth Medium and centrifuge at 250 × g for 5 minutes.

  3. Remove the supernatant and resuspend the cell pellet in 10 ml of Smooth Muscle Cell Growth Medium. Check cell number and viability.

  4. Divide the suspension between two 25 cm² culture flasks (5 ml each). Using two flasks reduces the risk of losing all cells if a passage fails.

  5. Incubate at 37 °C, 5 % CO₂ and saturated humidity, with the screw caps opened by half a turn for gas exchange.

  6. Change the medium after 24 hours to remove unattached cells, then every 48 to 72 hours, using pre-warmed medium only.

  7. Subculture the cells at about 75 % confluence. Denser cultures undergo irreversible contact inhibition and stop proliferating. Use the subculture reagents recommended on the certificate of analysis.

  8. Recommended seeding density: more than 4,000 cells/cm².

07Contrôle qualité et cryoconservation

Stérilité

Mycoplasma contamination is excluded by PCR.

To ensure there is no bacterial, fungal or yeast contamination, cultures are subjected to visual inspection.

Milieu de congélation
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Conditions de stockage

For long-term preservation, store vials in liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable for up to one week only.

Conditions de livraison

Cryopreserved primary cells are shipped on dry ice. On receipt, check the cryovial for damage and transfer it without delay to appropriate storage.

08Expression et sensibilité

Expression des protéines
Smooth muscle α-actin; calponin; smooth muscle myosin heavy chain
Virus
Free of HIV, Hepatitis B, Hepatitis C (confirmed negative by AddexBio)

09Identifiants

Référence
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
Numéro d'identification fiscale NCBI
9606
Cellosaurus
Not assigned

11Détails du produit

Tableau de composition