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Células del músculo liso de la arteria pulmonar humana (HPASMC)
Pañuelo de papel
Lung (pulmonary artery
Enfermedad
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Lugar de metástasis
Not applicable (normal, non-tumorigenic primary cell)
Sinónimos
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Documentos

Células del músculo liso de la arteria pulmonar humana (HPASMC)

Primary cell · Número de producto 300706

Músculo liso vascular pulmonar para la investigación sobre la HAP

€1,490.00sin impuestos ni gastos de envío

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01Descripción

02Información general

Descripción

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.

Pañuelo de papel
Lung (pulmonary artery
Enfermedad
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Lugar de metástasis
Not applicable (normal, non-tumorigenic primary cell)
Aplicaciones
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
Sinónimos
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Donante

Edad del donante
Lot-specific (see CoA)
Origen étnico
Lot-specific (see CoA)

04Clasificación

Organismo
Humano
Sexo
Específico de cada lote
Propiedades de crecimiento
Adherente
Situación respecto a los OMG
Sin OGM
Detalles sobre la presencia de OMG
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Nivel de bioseguridad
1

05Características

Morfología
Spindle-shaped (smooth muscle)
Tipo de célula
Primary smooth muscle cells
Tumorigénico
No
Tiempo de duplicación
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Manejo y cultivo

Medio de cultivo
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Atmósfera de incubación

37°C, 5% CO2, saturated humidity.

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

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.

Relación de división
1 to 3
Densidad de siembra
More than 4,000 cells/cm²
Renovación de fluidos
24 hours after seeding, then every 48 to 72 hours
Recuperación tras la descongelación

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

Descongelación y cultivo
  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.

07Control de calidad y criopreservación

Esterilidad

Mycoplasma contamination is excluded by PCR.

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

Medio de congelación
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Condiciones de almacenamiento

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.

Condiciones de envío

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

08Expresión y susceptibilidad

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

09Identificadores

Referencia
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
N.º de identificación fiscal del NCBI
9606
Cellosaurus
Not assigned

11Detalles del producto

Tabla de composición