Enteroendocrine cells release hormones and neurotransmitters to regulate nutrient absorption, digestion, motility, feeding behaviours and sensory perception.
One percent of the intestinal epithelium is represented by the Enteroendocrine Cells (EEC)
Based on their cytoarchitecture and location, Enteroendocrine Cells (EEC) are divided into open type, with a bottle-neck shape and a prolongation with microvilli in direct contact with the intestinal lumen, and closed type, strictly linked to the basal membrane, without reaching the intestinal lumen and without microvilli. Open-type cells are activated by luminal content, while closed-type EECs are sensitive to luminal contents through neural or humoral networks
Enteroendocrine cells (EEC) and their secreted product in the gut (aacording to )
| EECs | Location | Secreted products |
|---|---|---|
| A cell / A (X like) cells | Stomach:-:(corpus) (corpus) | Ghrelin |
| D cells | Stomach (pylorum) Proximal segment of the small intestine | Somatostatin |
| Enterochromaffin Cells (EC) | Stomach (pylorum) Small and large intestine | Melatonin, Serotonin, Substance P, in minor amounts: 4-Aminobutyric acid / GABA, Corticotropin-releasing hormone (CRH) (sometimes), Guanylin, Secretin, |
| G cells | Stomach (antrum) Duodenum | Gastrin |
| I cells | Small intestine Distal portion small intestine | Cholecystokinin (CCK) 5-HT / 5-Hydroxytryptamine / Serotonin |
| L cells | Distal portion of small intestine Colon (mainly in the proximal portion) Large intestine | Glucagon Like Peptide 1 (GLP-1) :-:\ Glucagon-like Peptide 2 (GLP-2) Peptide tyrosine tyrosine (Peptide YY / PYY) 5-HT / 5-Hydroxytryptamine / Serotonin |
| K cells | Small intestine | Gastric inhibitory polypeptide (GIP) 5-HT / 5-Hydroxytryptamine / Serotonin |
Enteroendocrine cells sense bacterial Tryptophan metabolites to activate enteric and vagus neuronal pathways
Enteroendocrine Cells sense nutrients and the metabolites from intestinal commensal microbiota and, in turn, coordinate antibacterial, mechanical, and metabolic branches of the host intestinal innate immune response to the commensal microbiota. After activation by various luminal stimuli they secrete hormones or neuronal messengers in a calcium-dependent manner
Short-chain fatty acids and branched-chain fatty acids from microbial carbohydrate and amino acid catabolism can activate Enteroendocrine Cells (EEC) via G protein-coupled receptors, a few studies show
Lu et al. 2018 Endocrinology 159(7): 2826-2835
Enteroendocrine cells (EECs) are not found in a consistent ratio throughout the gastrointestinal (GI) tract. Interestingly, all EECs exhibit plasticity, meaning they have the ability to revert to a stem cell state when there is damage or during treatments like chemotherapy or irradiation. Therefore, they can change their state when necessary.
New technical approaches showed that Enteroendocrine Cells (EEC) are derived from the endoderm and not the neuroectoderm, even if they share features with neurons
They arise from pluripotent stem cells at the base of the gut crypts and migrate up the crypt–villus axis; stem cells differentiate into Enteroendocrine Cells (EEC) over a period of 2–6 days thanks to three basic helix–loop–helix transcription factors. The same stem cells give rise to other epithelial cell types of the gut (enterocytes , Paneth , goblet cells ), and these cells are present in the villi and crypts of the gut
The hormones released by enteroendocrine cells can act locally, on other cells (including immune cells), on nerve endings, or on organs at distant sites, including pancreatic islets and the CNS.
Effects are: changes in food intake (appetite and satiety), changes in gastric emptying and intestinal transit, release of digestive enzymes, induction of nutrient transporters and digestive enzymes, increase in intestinal barrier function, insulin secretion by the pancreas, modulation of immune responses and tissue growth.
Enteroendocrine cells sense the metabolites from gut commensal microbiota. In turn, they coordinate the antibacterial, mechanical, and metabolic branches of the host intestinal innate immune response to the commensal microbiota.
In the year 1960, EECs were found to have markers for neuronal differentiation, and, for this reason, they were believed to originate from the neural crest and were named neuroendocrine cells
see also:
Enteroendocine Cell & G-Protein Coupled Receptor 41 (GPR41)