Vai al contenuto
Cellule muscolari lisce dell'arteria polmonare umana (HPASMC)
Tessuto
Lung (pulmonary artery
Malattia
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Sito metastatico
Not applicable (normal, non-tumorigenic primary cell)
Sinonimi
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Documenti

Cellule muscolari lisce dell'arteria polmonare umana (HPASMC)

Primary cell · Codice prodotto 300706

Muscolatura liscia vascolare polmonare per la ricerca sull’ipertensione arteriosa polmonare

€1,490.00IVA e spese di spedizione escluse

Personalizzazione / Suggerimenti

Su ordinazione
1

01Descrizione

02Informazioni generali

Descrizione

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.

Tessuto
Lung (pulmonary artery
Malattia
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Sito metastatico
Not applicable (normal, non-tumorigenic primary cell)
Applicazioni
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
Sinonimi
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Donatore

Età dei donatori
Lot-specific (see CoA)
Etnia
Lot-specific (see CoA)

04Classificazione

Organismo
Umano
Sesso
Specifico per lotto
Proprietà di crescita
Aderente
Presenza di OGM
Senza OGM
Dettagli sullo stato degli OGM
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Livello di biosicurezza
1

05Caratteristiche

Morfologia
Spindle-shaped (smooth muscle)
Tipo di cellula
Primary smooth muscle cells
Tumorigenico
No
Tempo di raddoppio
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Manipolazione e coltura

Terreno di coltura
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Atmosfera di incubazione

37°C, 5% CO2, saturated humidity.

Integratori
Supplement as specified in the AddexBio SMC supplement kit (refer to specification sheet). For cryopreservation: complete culture medium + 5% (v/v) DMSO.
Reagente di dissociazione
Subculture reagents as recommended on the certificate of analysis
Subcoltura

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.

Rapporto di frazionamento
1 to 3
Densità di semina
More than 4,000 cells/cm²
Rinnovo dei fluidi
24 hours after seeding, then every 48 to 72 hours
Recupero post-scongelamento

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

Scongelamento e coltura
  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.

07Controllo di qualità e crioconservazione

Sterilità

Mycoplasma contamination is excluded by PCR.

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

Terreno di coltura congelato
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Condizioni di conservazione

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.

Condizioni di spedizione

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

08Espressione e suscettibilità

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

09Identificatori

Riferimento bibliografico
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
Codice fiscale NCBI
9606
Cellosaurus
Not assigned

11Dettagli sul prodotto

Tabella delle composizioni