TY - JOUR
T1 - Detecting host responses to microbial stimulation using primary epithelial organoids
AU - Bornholdt, Jette
AU - Müller, Christina V
AU - Nielsen, Maria Juul
AU - Strickertsson, Jesper
AU - Rago, Daria
AU - Chen, Yun
AU - Maciag, Grzegorz
AU - Skov, Jonathan
AU - Wellejus, Anja
AU - Schweiger, Pawel J
AU - Hansen, Stine L
AU - Broholm, Christa
AU - Gögenur, Ismail
AU - Maimets, Martti
AU - Sloth, Stine
AU - Hendel, Jakob
AU - Baker, Adam
AU - Sandelin, Albin
AU - Jensen, Kim B
PY - 2023/12
Y1 - 2023/12
N2 - The intestinal epithelium is constantly exposed to microbes residing in the lumen. Traditionally, the response to microbial interactions has been studied in cell lines derived from cancerous tissues, e.g. Caco-2. It is, however, unclear how the responses in these cancer cell lines reflect the responses of a normal epithelium and whether there might be microbial strain-specific effects. To address these questions, we derived organoids from the small intestine from a cohort of healthy individuals. Culturing intestinal epithelium on a flat laminin matrix induced their differentiation, facilitating analysis of microbial responses via the apical membrane normally exposed to the luminal content. Here, it was evident that the healthy epithelium across multiple individuals (n = 9) demonstrates robust acute both common and strain-specific responses to a range of probiotic bacterial strains (BB-12Ⓡ, LGGⓇ, DSM33361, and Bif195). Importantly, parallel experiments using the Caco-2 cell line provide no acute response. Collectively, we demonstrate that primary epithelial cells maintained as organoids represent a valuable resource for assessing interactions between the epithelium and luminal microbes across individuals, and that these models are likely to contribute to a better understanding of host microbe interactions.
AB - The intestinal epithelium is constantly exposed to microbes residing in the lumen. Traditionally, the response to microbial interactions has been studied in cell lines derived from cancerous tissues, e.g. Caco-2. It is, however, unclear how the responses in these cancer cell lines reflect the responses of a normal epithelium and whether there might be microbial strain-specific effects. To address these questions, we derived organoids from the small intestine from a cohort of healthy individuals. Culturing intestinal epithelium on a flat laminin matrix induced their differentiation, facilitating analysis of microbial responses via the apical membrane normally exposed to the luminal content. Here, it was evident that the healthy epithelium across multiple individuals (n = 9) demonstrates robust acute both common and strain-specific responses to a range of probiotic bacterial strains (BB-12Ⓡ, LGGⓇ, DSM33361, and Bif195). Importantly, parallel experiments using the Caco-2 cell line provide no acute response. Collectively, we demonstrate that primary epithelial cells maintained as organoids represent a valuable resource for assessing interactions between the epithelium and luminal microbes across individuals, and that these models are likely to contribute to a better understanding of host microbe interactions.
KW - Intestinal organoids
KW - bacterial–epithelial interactions
KW - intestinal epithelium
KW - microbiome
KW - probiotics
UR - https://www.scopus.com/pages/publications/85177660872
U2 - 10.1080/19490976.2023.2281012
DO - 10.1080/19490976.2023.2281012
M3 - Journal article
C2 - 37992398
SN - 1949-0976
VL - 15
SP - 2281012
JO - Gut Microbes
JF - Gut Microbes
IS - 2
M1 - 2281012
ER -