Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2018 Mar 6;25(10):1732–1748. doi: 10.1038/s41418-018-0073-z

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© ADMC Associazione Differenziamento e Morte Cellulare 2018

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. If you remix, transform, or build upon this article or a part thereof, you must distribute your contributions under the same license as the original. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/.

PMC Copyright notice

Fig. 7 — In vivo analysis of the myocardin-miR133a-Nix pathway. a–d Sprague Dawley rats were subjected to left coronary artery ligation, or sham operation as a control. Following 4-weeks of recovery, the viable infarct border-zone was harvested from the left ventricle. Extracts were analyzed by real-time PCR for Myocardin (a), or miR-133a (b) expression (n = 4). Protein extracts were immunoblotted for Nix (c) expression and subjected to densitometry (d, n = 3). (E-H) C57BL6 mice received weekly intraperitoneal injections of doxorubicin (Dox; 8 mg/kg), or vehicle control, for 4 weeks. Extracts were analyzed by real-time PCR for Myocardin (e), or miR-133a (f) expression (n = 4). Protein extracts were immunoblotted for Nix (g) expression (n = 4) and subjected to densitometry (h). Data are expressed as mean ± SE. *p < 0.05 compared to control, determined by Student's T-test