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Glatte Muskelzellen der menschlichen Lungenarterie (HPASMC)
Gewebe
Lung (pulmonary artery
Krankheit
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Metastasenherd
Not applicable (normal, non-tumorigenic primary cell)
Synonyme
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Dokumente

Glatte Muskelzellen der menschlichen Lungenarterie (HPASMC)

Primary cell · Artikelnummer 300706

Glatte Muskulatur der Lungengefäße für die PAH-Forschung

€1,490.00zzgl. MwSt. und Versandkosten

Anpassung / Empfehlungen

Auftragsfertigung
1

01Beschreibung

02Allgemeine Informationen

Beschreibung

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.

Gewebe
Lung (pulmonary artery
Krankheit
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Metastasenherd
Not applicable (normal, non-tumorigenic primary cell)
Anwendungen
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
Synonyme
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Spender

Alter des Spenders
Lot-specific (see CoA)
Ethnische Zugehörigkeit
Lot-specific (see CoA)

04Klassifizierung

Organismus
Mensch
Sex
Los-spezifisch
Wachstumseigenschaften
Anhänger
GVO-Status
Ohne Gentechnik
Angaben zum GVO-Status
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Biologische Sicherheitsstufe
1

05Merkmale

Morphologie
Spindle-shaped (smooth muscle)
Zelltyp
Primary smooth muscle cells
Tumorauslösend
No
Verdopplungszeit
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Handhabung und Kultur

Nährmedium
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Inkubationsatmosphäre

37°C, 5% CO2, saturated humidity.

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

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.

Split-Verhältnis
1 to 3
Aussaatdichte
More than 4,000 cells/cm²
Flüssigkeitswechsel
24 hours after seeding, then every 48 to 72 hours
Erholung nach dem Auftauen

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

Auftauen und Kultivierung
  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.

07Qualitätskontrolle und Kryokonservierung

Sterilität

Mycoplasma contamination is excluded by PCR.

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

Gefriermedium
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Lagerbedingungen

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.

Versandbedingungen

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

08Expression und Anfälligkeit

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

09Bezeichner

Quellenangabe
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
NCBI-Steuer-ID
9606
Cellosaurus
Not assigned

11Produktdetails

Zusammensetzungstabelle