Ga naar de inhoud
Gladde spiercellen uit de menselijke longslagader (HPASMC)
Weefsel
Lung (pulmonary artery
Ziekte
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Plaats van uitzaaiingen
Not applicable (normal, non-tumorigenic primary cell)
Synoniemen
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Documenten

Gladde spiercellen uit de menselijke longslagader (HPASMC)

Primary cell · Productnummer 300706

Gladde spiercellen uit de longvaten voor onderzoek naar pulmonale arteriële hypertensie (PAH)

€1,490.00excl. btw en verzendkosten

Maatwerk / Aanbevelingen

Op bestelling gemaakt
1

01Beschrijving

02Algemene informatie

Beschrijving

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.

Weefsel
Lung (pulmonary artery
Ziekte
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Plaats van uitzaaiingen
Not applicable (normal, non-tumorigenic primary cell)
Toepassingen
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
Synoniemen
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Donateur

Leeftijd van de donor
Lot-specific (see CoA)
Etnische afkomst
Lot-specific (see CoA)

04Classificatie

Organisme
Mens
Seks
Lot-specifiek
Groei-eigenschappen
Aanhanger
GGO-status
Zonder genetisch gemodificeerde organismen
Details over de GGO-status
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Bioveiligheidsniveau
1

05Kenmerken

Morfologie
Spindle-shaped (smooth muscle)
Celtype
Primary smooth muscle cells
Tumorverwekkend
No
Verdubbelingstijd
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Behandeling en kweek

Kweekmedium
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Incubatieomgeving

37°C, 5% CO2, saturated humidity.

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

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.

Splitsingsverhouding
1 to 3
Zaaidichtheid
More than 4,000 cells/cm²
Vloeistofverversing
24 hours after seeding, then every 48 to 72 hours
Herstel na ontdooiing

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

Ontdooien en kweken
  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.

07Kwaliteitscontrole en cryopreservatie

Onvruchtbaarheid

Mycoplasma contamination is excluded by PCR.

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

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

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.

Verzendvoorwaarden

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

08Expressie en vatbaarheid

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

09Identificatiegegevens

Bronvermelding
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
NCBI-belastingnummer
9606
Cellosaurus
Not assigned

11Productgegevens

Overzichtstabel