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Células do músculo liso da artéria pulmonar humana (HPASMC)
Tecido
Lung (pulmonary artery
Doença
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Local da metástase
Not applicable (normal, non-tumorigenic primary cell)
Sinónimos
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

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Células do músculo liso da artéria pulmonar humana (HPASMC)

Primary cell · Número do produto 300706

Músculo liso vascular pulmonar para investigação sobre a HAP

€1,490.00sem impostos nem portes de envio

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01Descrição

02Informações gerais

Descrição

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.

Tecido
Lung (pulmonary artery
Doença
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Local da metástase
Not applicable (normal, non-tumorigenic primary cell)
Aplicações
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

03Doador

Idade do dador
Lot-specific (see CoA)
Etnia
Lot-specific (see CoA)

04Classificação

Organismo
Humano
Sexo
Específico do lote
Propriedades de crescimento
Aderente
Estatuto em matéria de OGM
Sem OGM
Detalhes sobre o estatuto dos OGM
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Nível de biossegurança
1

05Características

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

06Manuseamento e cultura

Meio de cultura
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Atmosfera de incubação

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.
Reagente de dissociação
Subculture reagents as recommended on the certificate of analysis
Subcultura

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.

Rácio de divisão
1 to 3
Densidade de sementeira
More than 4,000 cells/cm²
Renovação de fluidos
24 hours after seeding, then every 48 to 72 hours
Recuperação após o descongelamento

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

Descongelamento e cultura
  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.

07Controlo de qualidade e criopreservação

Esterilidade

Mycoplasma contamination is excluded by PCR.

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

Meio de congelação
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Condições de armazenamento

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.

Condições de envio

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

08Expressão e suscetibilidade

Expressão proteica
Smooth muscle α-actin; calponin; smooth muscle myosin heavy chain
Vírus
Free of HIV, Hepatitis B, Hepatitis C (confirmed negative by AddexBio)

09Identificadores

Referência
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
Número de identificação fiscal do NCBI
9606
Cellosaurus
Not assigned

11Detalhes do produto

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