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Ha vsmcs

Manufactured by ScienCell
Sourced in United States

HA-VSMCs are primary human aortic vascular smooth muscle cells. They are isolated from the human aorta and are cryopreserved at the end of the primary culture. HA-VSMCs retain their normal morphology and functionality.

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4 protocols using ha vsmcs

1

Modulation of VSMC Calcification by Exosomes

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Human aortic vascular smooth muscle cells (HA-VSMCs, ScienCell, USA) were cultured in SMC medium (ScienCell, USA) supplemented with 2% FBS. Human BMSCs were cultured in MSC medium supplemented with 5% exosome-depleted FBS (ScienCell, USA).
To induce calcification, HA-VSMCs were treated with 2.5 mmol/L Pi for 14 days. To observe the contribution of exosomes and NONHSAT 084969.2 on calcification, HA-VSMCs were treated with 100 μg/ml BMSC-Exos or small interfering RNA NONHSAT 084969.2 (si-NONHSAT 084969.2) for 14 days. Finally, calcification and osteogenic transdifferentiation were evaluated.
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2

Inorganic Phosphate-Induced VSMC Calcification

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HA-VSMCs were obtained from ScienCell Research Laboratories (CA, USA), and were cultured in SMC medium containing 2% fetal bovine serum (FBS). HA-VSMCs were stimulated with inorganic phosphate (final concentration 2.5 mM, pH 7.4) (Sigma-Aldrich, MI, USA) to induce calcification [41 (link)]. Cells in our experiments were all tested for short tandem repeat analysis and were free of mycoplasma contamination.
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3

Aortic Smooth Muscle Cell Calcification

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Human aortic smooth muscle cells (HA-VSMCs) was purchased from ScienCell (USA). An VSMC culture medium containing 10% fetal bovine serum, 1% penicillin-streptomycin and 1% growth supplement (ScienCell, USA) was cultured in incubators with 5% CO2 at 37 °C. Once cells had grown to 90% confluence in the Petri dish, 0.25% trypsin (Sigma, USA) was added for harvesting. The passage ratio was 1:3. HA-VSMCs from the fourth to sixth passage were used in subsequent experiments. The cells were cultured in Dulbecco’s Modified Eagle’s Medium (contained 2.5 mM Na2HPO4) for 7 days to induce calcification. The medium was replaced every other day.
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4

HA-VSMC Culture and Oxidized LDL Exposure

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HA-VSMCs were provided by the American Type Culture Collection (ATCC; Rockville, MD, USA). HA-VSMCs were maintained in SMC medium (SMCM; ScienCell, Carlsbad, CA, USA) and cultured in an incubator containing 5% CO2 at 37 ℃. HA-VSMCs were passaged every 3–4 days. The medium was added with 1% penicillin-streptomycin and 2% fetal bovine serum (Gibco, Thermo Fisher Scientific, Waltham, MA, USA). HA-VSMCs were incubated for 24 h. Oxidized LDL (ox-LDL) was prepared at concentrations of 25, 50, 75, and 100 µg/mL.
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