# A Quantity-Dependent Nonlinear Model of Sodium Cromoglycate Suppression on Beta-Conglycinin Transport

**Authors:** Ziang Zheng, Junfeng Han, Xinyi Chen, Shugui Zheng

PMC · DOI: 10.3390/ijms25126636 · 2024-06-17

## TL;DR

This study explores how a substance called sodium cromoglycate can block the absorption of a soybean allergen in intestinal cells.

## Contribution

The study reveals a new nonlinear model of suppression by sodium cromoglycate on allergen transport.

## Key findings

- Beta-conglycinin hydrolysates are absorbed through a transcellular pathway in IPEC-J2 monolayers.
- Sodium cromoglycate suppresses allergen transport in a quantity-dependent nonlinear manner.
- Clathrin-mediated and caveolae-dependent endocytosis mechanisms are involved in allergen transport.

## Abstract

Understanding the transport mechanism is crucial for developing inhibitors that block allergen absorption and transport and prevent allergic reactions. However, the process of how beta-conglycinin, the primary allergen in soybeans, crosses the intestinal mucosal barrier remains unclear. The present study indicated that the transport of beta-conglycinin hydrolysates by IPEC-J2 monolayers occurred in a time- and quantity-dependent manner. The beta-conglycinin hydrolysates were absorbed into the cytoplasm of IPEC-J2 monolayers, while none were detected in the intercellular spaces. Furthermore, inhibitors such as methyl-beta-cyclodextrin (MβCD) and chlorpromazine (CPZ) significantly suppressed the absorption and transport of beta-conglycinin hydrolysates. Of particular interest, sodium cromoglycate (SCG) exhibited a quantity-dependent nonlinear suppression model on the absorption and transport of beta-conglycinin hydrolysates. In conclusion, beta-conglycinin crossed the IPEC-J2 monolayers through a transcellular pathway, involving both clathrin-mediated and caveolae-dependent endocytosis mechanisms. SCG suppressed the absorption and transport of beta-conglycinin hydrolysates by the IPEC-J2 monolayers by a quantity-dependent nonlinear model via clathrin-mediated and caveolae-dependent endocytosis. These findings provide promising targets for both the prevention and treatment of soybean allergies.

## Linked entities

- **Chemicals:** methyl-beta-cyclodextrin (PubChem CID 51051622), chlorpromazine (PubChem CID 2726), sodium cromoglycate (PubChem CID 27503)

## Full-text entities

- **Diseases:** allergic reactions (MESH:D004342)
- **Chemicals:** MbetaCD (MESH:C108732), CPZ (MESH:D002746), SCG (MESH:D004205)
- **Species:** Glycine max (soybean, species) [taxon 3847]
- **Cell lines:** IPEC-J2 — Sus scrofa (Pig), Spontaneously immortalized cell line (CVCL_2246)

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11204204/full.md

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Source: https://tomesphere.com/paper/PMC11204204