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Glatte muskelceller fra menneskelig lungearterie (HPASMC)
Vev
Lung (pulmonary artery
Sykdom
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Metastaseområde
Not applicable (normal, non-tumorigenic primary cell)
Synonymer
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Dokumenter

Glatte muskelceller fra menneskelig lungearterie (HPASMC)

Primary cell · Produktnummer 300706

Glatt muskulatur i lungekarene til forskning på pulmonal arteriell hypertensjon (PAH)

€1,490.00ekskl. mva. og frakt

Tilpasning / Anbefalinger

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01Beskrivelse

02Generell informasjon

Beskrivelse

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.

Vev
Lung (pulmonary artery
Sykdom
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Metastaseområde
Not applicable (normal, non-tumorigenic primary cell)
Søknader
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
Synonymer
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Donor

Donorens alder
Lot-specific (see CoA)
Etnisitet
Lot-specific (see CoA)

04Klassifisering

Organisme
Menneske
Sex
Tomtespesifikk
Vekstegenskaper
Tilhenger
GMO-status
Uten GMO
Detaljer om GMO-status
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Biosikkerhetsnivå
1

05Egenskaper

Morfologi
Spindle-shaped (smooth muscle)
Celletype
Primary smooth muscle cells
Tumorinduserende
No
Fordoblingstid
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Håndtering og kultur

Næringsmedium
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Inkubasjonsatmosfære

37°C, 5% CO2, saturated humidity.

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

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.

Oppdelingsforhold
1 to 3
Såtetthet
More than 4,000 cells/cm²
Væskefornyelse
24 hours after seeding, then every 48 to 72 hours
Gjenoppretting etter tining

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

Tining og dyrking
  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.

07Kvalitetskontroll og kryokonservering

Sterilitet

Mycoplasma contamination is excluded by PCR.

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

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

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.

Fraktvilkår

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

08Uttrykk og mottakelighet

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

09Identifikatorer

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

11Produktdetaljer

Sammensetningstabell