Table 1.
Summary of current intestine models.
Intestinal models | Advantage | Limitation | Ref. |
---|---|---|---|
Intestine animal models | Traditional model; Technology maturity; Approaching the stage of clinical studies. | long time cycles; expensive; racial differences from human; subject to animal ethics. | [15, 16] |
2D intestine cellular model | The culture is simple, the technology is mature, the cost is low, and it is adapted to simple preclinical studies. | Planar culture environment, monolayer cell culture, gradually planarizing and losing differentiation phenotype, inability to form intestinal epithelial structures. | [168–173] |
3D intestine organoid model | 3D culture environment that mimics the growth environment of ISCs in vivo, forms intestinal epithelial structures, and maintains stable phenotypic and genetic characteristics. | Culture process and technology is relatively complex, and cost is relatively high. There are still limitations that hinder clinical translation. | [174–178] |
Intestine Organoid microarray | More precise regulation of the cultivation environment, simulating the physical and microbial environment in the body. | The culture system and process lack standards, the culture technology needs to be improved, and the cost is high. | [179–184] |