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. 2023 Sep 22;23:326. doi: 10.1186/s12876-023-02944-8

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© The Author(s) 2023

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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — mRNA expression and protein levels of autophagic core proteins in AGS cells infected with Helicobacter pylori. A Western blotting analysis of autophagy-related proteins in AGS cells infected with Hp-WT and Hp-ΔcagA. Quantification of ATG5, ATG7, Beclin1, and ULK1 signal intensity (n = 4, mean ± SD, *P < 0.05). B) mRNA expression levels of ATG5 and BECN1 in AGS cells infected with Hp-WT and Hp-ΔcagA analysed using q-RT PCR (n = 6, mean ± SD, *P < 0.05). ATG5, autophagy related 5; Hp-WT, wild-type cagA-positive H. pylori; Hp-ΔcagA, cagA-knockout H. Pylori; q-RT PCR, quantitative reverse transcription-polymerase chain reaction; SD, standard deviation