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. 2022 Aug 16;8:364. doi: 10.1038/s41420-022-01144-9

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© The Author(s) 2022

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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Fig. 4 — a RNA pulldown assays were performed, and the lnc5745-related proteins were determined with SDS-polyacrylamide gel electrophoresis (SDS–PAGE) and Coomassie brilliant blue staining. b List of lnc5745-related proteins identified by mass spectrometry (MS). c Western blot analysis confirmed the existence of Rab2A in lnc5745-related proteins. d, e Binding of Rab2A to lnc5745 was confirmed by qPCR and PCR after RNA immunoprecipitation (RIP). f–h Rab2A levels were negatively affected by lnc5745 in NMVCs. i Effect of lnc5745 overexpression on Rab2A expression after CHX treatment for 0, 4, 8, 12 and 16 hours. j Effect of lnc5745 knockdown on Rab2A expression after CHX treatment for 0, 4, 8, 12 and 16 hours. k Effect of MG132 treatment for 12 hours on the stability of Rab2A protein. The results are from three independent experiments, *P < 0.05. Variables are presented as the mean ± SD.