CN354-05

Sigma-Aldrich

Canine Aortic Smooth Muscle Cells: CnAOSMC (Cryovial)

biological source

canine aorta (normal, tunica intima and media)

packaging

pkg of 500,000 cells

growth mode

Adherent

karyotype

2n = 78

morphology

smooth muscle

application(s)

cell culture | mammalian: suitable

relevant disease(s)

cardiovascular diseases

shipped in

dry ice

storage temp.

−196°C

Related Categories

General description

Canine Aortic Smooth Muscle Cells (CnAOSMC) are derived from tunica intima and tunica media of normal canine aorta. They are cryopreserved at second passage and can be cultured and propagated at least 10 population doublings. Platelet-derived growth factor (PDGF) is a potent mitogen and chemotactic agent which may be involved in intimal hyperplasia and atherosclerosis. It was shown that significant regional difference in PDGF production in normal canine aorta, and that SMC are a significant contributor to the regional variation in PDGF production.

1. It was also shown that nebivolol relaxes vascular smooth muscle by NO- and cyclic GMP-dependent mechanisms.
2. Graft SMCs are functionally altered producing more platelet-derived growth factor (PDGF) than aortic SMCs. PDGF produced by graft SMCs may contribute to the development of intimal hyperplasia.
3. Graft SMCs have decreased proliferation response, but have similar migratory response to PDGF compared with aortic SMCs.
4. Intrinsic differences in endothelial cells from proximal aorta versus the distal aorta have different capacity to produce PDGF in response to stimulants whereas unstimulated SMCs did not exhibit regional variation in PDGF production and did not increase PDGF secretion after PMA or thrombin treatment.
5. Identification of the cDNA for canine isoform of nitric oxide synthase (iNOS) can be used in the study of allograft rejection and cardiovascular disease.

RECENT PUBLICATIONS Kiyan, Y., S. Tkachuk, D. Hilfker-Kleiner, H. Haller, B. Fuhrman, and Inna Dumler. 2014. oxLDL induces inflammatory responses in vascular smooth muscle cells via urokinase receptor association with CD36 and TLR4. J Molec and Cell Cardiol, 66:72-82.

Ignarro, L.J. et al, Nitric Oxide. 7(2):75-82 (2002).
Madura, J.A. et al, J. Vas Res. 33(1):53-61 (1996).
Pitsch, R.J. et al, J. Vasc. Surg. 26(1):70-8 (1997).
Minion, D.J. et al, J. Vasc. Surg. 31(5):953-9 (2000).
Van Aalst, J.A. et al, J. Vasc. Surg. 32(3):584-92 (2000).
Wang, X. et al, Am. J. Physiol. 275(4 Pt 2):H1122-9 (1998).

Products are for research use only. They are not intended for human, animal, or diagnostic applications.

Cell Line Origin

Aorta

Application

aortic wall contraction, role of smc under normal conditions, blood pressure, distribution of oxygenated blood through systemic circulation

Components

Canine Smooth Muscle Cell Basal Medium containing 10% FBS & 10% DMSO

Preparation Note

  • 2nd passage, >500,000 cells in Canine Smooth Muscle Cell Basal Medium containing 10% FBS & 10% DMSO
  • Can be cultured at least 10 doublings

Subculture Routine

Please refer to the CnAOSMC Culture Protocol.

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis
Certificate of Origin
Protocols
Technical information for working with Canine Aortic Smooth Muscle Cells including thawing, subculturing and cryopreservation
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