RT Journal Article
T1 A non‐fluorescent immunohistochemistry method for measuring autophagy flux using MAP1LC3/LC3 and SQSTM1 as core markers
A1 Shojaei, Shahla
A1 Barzegar Behrooz, Amir
A1 Cordani, Marco
A1 Aghaei, Mahmoud
A1 Azarpira, Negar
A1 Klionsky, Daniel J.
A1 Ghavami, Saeid
AB Macroautophagy/autophagy is a crucial cellular process for degrading and recycling damaged proteins and organelles, playing a significant role in diseases such as cancer and neurodegeneration. Evaluating autophagy flux, which tracks autophagosome formation, maturation, and degradation, is essential for understanding disease mechanisms. Current fluorescence-based methods are resource-intensive, requiring advanced equipment and expertise, limiting their use in clinical laboratories. Here, we introduce a non-fluorescent immunohistochemistry (IHC) method using MAP1LC3/LC3 and SQSTM1 as core markers for autophagy flux assessment. LC3 levels reflect autophagosome formation, whereas SQSTM1 degradation and a decrease in the number of its puncta indicate active flux (i.e., lysosomal turnover). We optimized chromogenic detection using diaminobenzidine (DAB) staining and developed a scoring system based on puncta number and the percentage of stained cells. This accessible, cost-effective method enables reliable autophagy quantification using a standard light microscope, bridging the gap between experimental research and clinical diagnostics. Our protocol allows accurate autophagy evaluation in fixed tissues, offering practical applications in biomedical research and clinical pathology assessment.
PB John Wiley & Sons
SN 2211-5463
YR 2025
FD 2025-04-03
LK https://hdl.handle.net/20.500.14352/120134
UL https://hdl.handle.net/20.500.14352/120134
LA eng
NO Shojaei, S., Barzegar Behrooz, A., Cordani, M., Aghaei, M., Azarpira, N., Klionsky, D. J., & Ghavami, S. (2025). A non-fluorescent immunohistochemistry method for measuring autophagy flux using MAP1LC3/LC3 and SQSTM1 as core markers. FEBS Open Bio . https://doi.org/10.1002/2211-5463.70014
NO M.C. is supported by grant RYC2021-031003I funded by MICIU/AEI/https://doi.org/10.13039/501100011033 and, by European Union NextGenerationEU/PRTR; DJK is funded by National Institutes of Health/https://doi.org/10.13039/100000002 grant GM131919. SG was supported by CCMF Operating grant (763117252).
NO Ministerio de Ciencia, Innovación y Universidades (España)
NO European Commission
NO Universidad Complutense de Madrid
DS Docta Complutense
RD 17 may 2025