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Supplementary Figure 3. Traction force microscopy quantification of TGFβ stimulated IMR-90 cells with 5 µM siRNA (non-targeting, ACTA2, CNN1, TAGLN).

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posted on 2021-09-23, 18:43 authored by Patrick LinkPatrick Link, haak.andrew@mayo.edu, Tschumperlin.daniel@mayo.edu, choi.kyoung@mayo.edu, diazespinosa.ana@mayo.edu, Dakota.jones@pennmedicine@upenn.edu, gao.ashley@mayo.edu
A) IMR-90 cells treated for 72 hours +/- 2 ng/ml TGFβ1 in the presence of 5 µM siRNA (non-targeting, ACTA2, CNN1, TAGLN) were passaged onto microsphere and collagen-coated polyacrylamide substrates with an Elastic modulus of 25 kPa overnight before traction-force measurements. Points are individuals cell measurements from 2 independent experiments. B-D) qPCR confirmation of mRNA knockdown for ACTA2 (B), CNN1 (C), and TAGLN (D).

Funding

NIH HL092961

NIH HL105355

Boehringer Ingelheim (BI) Discovery Award in Interstitial Lung Disease

American Lung Association (Lung Association) Catalyst Award

Pulmonary Fibrosis Foundation (PFF) Scholars Award

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