Spatial Proteomics Reveals Alcohol-Induced Damages to the Crypts and Villi of the Mouse Small Intestine.
Patil Shivprasad SureshXinguo SunZhanxiang ZhouQibin ZhangPublished in: Journal of proteome research (2024)
Alcohol consumption perturbs the gut immune barrier and ultimately results in alcoholic liver diseases, but little is known about how immune-related cells in the gut are perturbed in this process. In this study, we employed laser capture microdissection and a label-free proteomics approach to investigate the consequences of alcohol exposure to the proteomes of crypts and villi in the proximal small intestine. Intestinal tissues from alcohol-fed and pair-fed mice were microdissected to selectively capture cells in the crypts and villi regions, followed by one-pot protein digestion and data-independent LC-MS/MS analysis. We successfully identified over 3000 proteins from each of the crypt or villi regions equivalent to ∼3000 cells. Analysis of alcohol-treated tissues indicated an enhanced alcohol metabolism and reduced levels of α-defensins in crypts, alongside increased lipid metabolism and apoptosis in villi. Immunofluorescence imaging further corroborated the proteomic findings. Our work provides a detailed profiling of the proteomic changes in the compartments of the mouse small intestine and aids in molecular-level understanding of alcohol-induced tissue damage.
Keyphrases
- alcohol consumption
- label free
- cell cycle arrest
- induced apoptosis
- cell death
- endoplasmic reticulum stress
- oxidative stress
- gene expression
- mass spectrometry
- pi k akt
- skeletal muscle
- type diabetes
- high resolution
- machine learning
- adipose tissue
- metabolic syndrome
- drug induced
- cell proliferation
- insulin resistance
- single cell
- photodynamic therapy
- fatty acid
- protein protein
- stress induced
- high fat diet induced