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. 2019 Feb 14;9:2059. doi: 10.1038/s41598-019-39515-5

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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. 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/4.0/.

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Thbs4-mediated ER expansion and upregulation of ER stress-associated proteins requires ATF6α. (a) Transmission electron micrograph of sections from Thbs4 DTG, Thbs4 DTG and Atf6^−/−, or Thbs4 DTG and Atf6b^−/− hearts. Arrows mark areas of increased ER and the post ER-vesicular compartment. (b) Representative immunoblots for the indicated ER stress-associated proteins from heart homogenates of control, Atf6^−/−, Thbs4, or Thbs4 Atf6^−/− mice.