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Células del músculo liso urotelial humano (HUSMC)
Pañuelo de papel
Bladder
Enfermedad
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Lugar de metástasis
Not applicable (normal, non-tumorigenic primary cell)
Sinónimos
HBdSMC, HUSMC, Human urothelial smooth muscle cells, provitro 1210631

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Células del músculo liso urotelial humano (HUSMC)

Primary cell · Número de producto 300707

Músculo liso del tracto urinario para la investigación en urología

€1,220.00sin impuestos ni gastos de envío

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01Descripción

02Información general

Descripción

Primary Human Bladder Smooth Muscle Cells (HBdSMC) are isolated from the smooth muscle layer of the urinary tract. They are used to study the response of the bladder wall to mechanical stretch and as a building block for engineered bladder tissue.

HBdSMC respond to cyclic stretch and hydrostatic pressure that mimic bladder filling with increased proliferation and altered contractility, involving muscarinic receptor signaling. This makes them a model for detrusor remodeling in bladder outlet obstruction and for conditioning cells in bladder tissue engineering.

Pañuelo de papel
Bladder
Enfermedad
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Lugar de metástasis
Not applicable (normal, non-tumorigenic primary cell)
Aplicaciones
Cyclic stretch of the bladder wall, muscarinic receptors and proliferation; Hydrostatic pressure in bladder outlet obstruction: proliferation and contractility; Hypoxia and oxidative stress in bladder ischemia; Rac1 signaling as a target in overactive bladder; Bladder tissue engineering with urothelial and smooth muscle cells
Sinónimos
  • HBdSMC
  • HUSMC
  • Human urothelial smooth muscle cells
  • provitro 1210631

03Donante

Edad del donante
Lot-specific (see CoA)
Origen étnico
Lot-specific (see CoA)

04Clasificación

Organismo
Humano
Sexo
Específico de cada lote
Propiedades de crecimiento
Adherente
Situación respecto a los OMG
Sin OGM
Detalles sobre la presencia de OMG
No genetic modification; primary human bladder smooth muscle cells. Not transformed or immortalized. Confirmed negative for mycoplasma, bacteria, yeast, HIV-1, HBV, HCV.
Nivel de bioseguridad
1

05Características

Morfología
Spindle-shaped (smooth muscle)
Tipo de célula
Primary smooth muscle cells
Tumorigénico
No
Tiempo de duplicación
approx. 18 to 36 hours (lot-specific; AcceGen equivalent: ~13 population doublings guaranteed)

06Manejo y cultivo

Medio de cultivo
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Atmósfera de incubación

37°C, 5% CO2, saturated humidity.

Suplementos
Supplement per AcceGen medium kit instructions. Standard SMC growth medium contains FBS (5–10%), EGF, FGF, and insulin as major components. Refer to product-specific CoA.
Reactivo de disociación
Subculture reagents as recommended on the certificate of analysis
Subcultivo

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.

Relación de división
1 to 3
Densidad de siembra
More than 4,000 cells/cm²
Renovación de fluidos
24 hours after seeding, then every 48 to 72 hours
Recuperación tras la descongelación

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

Descongelación y cultivo
  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.

07Control de calidad y criopreservación

Esterilidad

Mycoplasma contamination is excluded by PCR.

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

Medio de congelación
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Condiciones de almacenamiento

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.

Condiciones de envío

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

08Expresión y susceptibilidad

Antígenos de superficie
α-smooth muscle actin (α-SMA) +; Desmin +; Calponin (CNN1) +; SM-MHC (MYH11) + (differentiated); h-caldesmon + (differentiated); γ-smooth muscle actin + (differentiated); Connexin 43 +
Receptores expresados
Muscarinic acetylcholine receptor M2 (CHRM2) +; Muscarinic receptor M3 (CHRM3) +; PDGFR-β (CD140b); Adrenergic receptors (β1, β3)
Virus
Free of HIV-1, HBV, HCV (confirmed negative; AcceGen ABC-TC3862 QC)

09Identificadores

Referencia
Human urothelial smooth muscle cells (HUSMC) (Cytion catalog number 300707)
N.º de identificación fiscal del NCBI
9606
Cellosaurus
Not assigned

11Detalles del producto

Tabla de composición