Optimization of the <i>in</i> <i>vitro</i> culture system for chicken small intestinal organoids.

Jing LI; Liya WANG; Dingyun MA; Senyang LI; Juanfeng LI; Qingda MENG; Junqiang LI; Fuchun JIAN

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Optimization of the in vitro culture system for chicken small intestinal organoids.

Author: Jing LI ¹ ; Liya WANG ¹ ; Dingyun MA ¹ ; Senyang LI ¹ ; Juanfeng LI ¹ ; Qingda MENG ¹ ; Junqiang LI ¹ ; Fuchun JIAN ¹
Author Information

1. College of Veterinary Medicine, Henan Agricultural University, Zhengzhou 450002, Henan, China.
Publication Type:Journal Article
Keywords: chicken small intestinal organoids; crypt; intestinal stem cell; small intestine
MeSH: Animals; Organoids/metabolism*; Intestine, Small/drug effects*; Chickens; Cell Culture Techniques/methods*; Culture Media; Chick Embryo; Tissue Culture Techniques/methods*
From: Chinese Journal of Biotechnology 2024;40(12):4645-4659
CountryChina
Language:Chinese
Abstract: In order to establish a stable in vitro culture platform for chicken small intestine three-dimensional (3D) organoids, in this study, crypt cells were collected from the small intestine of 18-day-old embryos of AA broilers. On the basis of the L-WRN conditioned medium, we optimized the culture conditions of chicken small intestinal organoids by adjusting the proportions of nicotinamide, N-acetylcysteine, LY2157299, CHIR99021, Jagged-1, FGF, and other cytokines to select the medium suitable for the long-term stable growth of the organoids. The optimization results showed that the addition of 1.5 µmol/L CHIR99021 significantly improved the organoid formation efficiency and organoid diameter. When 0.5 µmol/L Jagged-1 was added, a small amount of bud-like tissue appeared in organoids. After the addition of 50 ng/mL FGF-2, the rate of organoid germination was significantly increased. The 1.5 µmol/L CHIR99021, 0.5 µmol/L Jagged-1, and 50 ng/mL FGF-2 added in the medium can cooperate with each other to improve the formation and speed up the proliferation and differentiation of organoids, while improving the stemness maintenance of cells. The morphology, cell types, and culture characteristics of chicken small intestinal organoids were studied by HE staining, transmission electron microscopy, reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR), indirect immunofluorescence, and immunohistochemistry. The results showed that the 3D organoids of the chicken small intestine cultured in vitro were morphologically consistent with the chicken intestinal tissue and contained differentiated epithelial cells. In summary, we successfully established an in vitro culture system for chicken small intestinal organoids, providing a new method for the subsequent research on chicken intestinal physiology, pathology, and host-pathogen interaction mechanism and the development of relevant drugs.