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Updated: Jul 15, 2026

Generation and Manipulation of Rat Intestinal Organoids
Published on: June 23, 2023
Acylase 1 expression in rat intestinal crypt--villus axis
Natacha Cigna1, Cendrine Nicoletti, Anne Durand
1BiosCiences FRE CNRS 3005, Université Paul Cézanne - Aix-Marseille III, Faculté des Sciences, 13397 Marseille Cedex 20, France.
Acylase 1 (ACY 1) activity and mRNA expression are significantly higher in rat intestinal crypt cells compared to differentiated villus cells. This suggests ACY 1 is a novel marker for intestinal absorbing cells, regulated at the mRNA level.
Area of Science:
- Cell Biology
- Gastroenterology
- Molecular Biology
Background:
- The small intestine's epithelial lining undergoes continuous renewal through cell differentiation.
- Understanding gene expression patterns during enterocyte differentiation is crucial for intestinal health research.
Purpose of the Study:
- To investigate the cellular localization and expression regulation of Acylase 1 (ACY 1) in the rat small intestine.
- To determine if ACY 1 can serve as a marker for specific intestinal cell types.
Main Methods:
- Separation of rat jejunal villus tip and crypt cells using the Weiser method.
- Measurement of ACY 1 activity in isolated cell populations.
- Quantitative analysis of ACY 1 mRNA expression via RT-PCR.
- Immunohistochemical localization of ACY 1 protein.
Main Results:
- Undifferentiated crypt cells exhibited significantly higher ACY 1 activity (6.4-fold decrease along differentiation axis) and mRNA levels (12-fold higher in crypt cells) compared to villus cells.
- ACY 1 expression is primarily regulated at the mRNA level in intestinal crypt cells.
- Immunohistochemistry confirmed ACY 1 expression in absorbing lineage cells of ileal and colonic crypts, but not in goblet cells.
Conclusions:
- Acylase 1 (ACY 1) is highly expressed in rat intestinal crypt cells and its expression is regulated at the mRNA level.
- ACY 1 is proposed as a novel marker transcript for intestinal absorbing cells.
- This finding aids in monitoring intestinal N-alpha-acetylated protein metabolism.
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