Host-microbiota interaction in intestinal stem cell homeostasis

Gut Microbes. 2024 Jan-Dec;16(1):2353399. doi: 10.1080/19490976.2024.2353399. Epub 2024 May 17.

Abstract

Intestinal stem cells (ISCs) play a pivotal role in gut physiology by governing intestinal epithelium renewal through the precise regulation of proliferation and differentiation. The gut microbiota interacts closely with the epithelium through myriad of actions, including immune and metabolic interactions, which translate into tight connections between microbial activity and ISC function. Given the diverse functions of the gut microbiota in affecting the metabolism of macronutrients and micronutrients, dietary nutrients exert pronounced effects on host-microbiota interactions and, consequently, the ISC fate. Therefore, understanding the intricate host-microbiota interaction in regulating ISC homeostasis is imperative for improving gut health. Here, we review recent advances in understanding host-microbiota immune and metabolic interactions that shape ISC function, such as the role of pattern-recognition receptors and microbial metabolites, including lactate and indole metabolites. Additionally, the diverse regulatory effects of the microbiota on dietary nutrients, including proteins, carbohydrates, vitamins, and minerals (e.g. iron and zinc), are thoroughly explored in relation to their impact on ISCs. Thus, we highlight the multifaceted mechanisms governing host-microbiota interactions in ISC homeostasis. Insights gained from this review provide strategies for the development of dietary or microbiota-based interventions to foster gut health.

Keywords: Intestinal stem cells; dietary nutrients; gut homeostasis; immune homeostasis; intestinal organoid; metabolic interaction; microbiome; micronutrients.

Publication types

  • Review

MeSH terms

  • Animals
  • Bacteria / classification
  • Bacteria / metabolism
  • Gastrointestinal Microbiome* / physiology
  • Homeostasis*
  • Host Microbial Interactions*
  • Humans
  • Intestinal Mucosa* / metabolism
  • Intestinal Mucosa* / microbiology
  • Intestines / microbiology
  • Stem Cells* / metabolism

Grants and funding

This work was supported by the National Natural Science Foundation of China [under Grant number 32030104] and the National Key R&D Program of China [under Grant number 2022YFD1300402].