Intestinal crypts
Glandulae intestinales
Also known as: crypts of Lieberkühn, intestinal glands
Intestinal crypts (of Lieberkühn) are simple tubular glands that dip from the mucosal surface down to the muscularis mucosae. They hold the stem cells that renew the epithelium, and they secrete fluid, mucus and antimicrobial proteins.
Overview
In the small intestine the crypts open between the bases of the villi. In the large intestine they open on the flat mucosal surface, where they are straight, closely packed and very rich in goblet cells.
At the crypt base, Lgr5⁺ crypt-base columnar stem cells sit between Paneth cells, which secrete antimicrobial proteins and supply niche signals (Wnt, EGF and Notch ligands). Above them, rapidly dividing transit-amplifying cells produce all the epithelial lineages: enterocytes, goblet cells, enteroendocrine cells (I, S, K, L and serotonin-secreting enterochromaffin cells) and tuft cells. This is the fastest-renewing tissue in the adult body.
Crypt enterocytes are the main secretory cells of the intestine. Cl⁻ enters basolaterally on the Na⁺-K⁺-2Cl⁻ co-transporter (NKCC1) and leaves apically through CFTR. Na⁺ and water follow through the paracellular pathway. The result is about 1.8 L a day of isotonic, slightly alkaline intestinal juice, which keeps luminal contents fluid and flushes the crypts.
- Location
Throughout the mucosa of the small and large intestine and the appendix, between and below the villi.
Parts & subdivisions
- Lgr5⁺ stem cells at the crypt base, alternating with Paneth cells.
- Granule-filled defensive cells at the crypt base of the small intestine.
- Transit-amplifying zoneRapidly proliferating progenitors in the lower and middle crypt.
- Enteroendocrine cellsScattered hormone-secreting cells (CCK, secretin, GIP, GLP-1, serotonin and others).
Anatomy
- Histology
Simple tubular glands lined by simple columnar epithelium, with Paneth cells at the base in the small intestine and many goblet cells in the colon.
Function
- Renew the intestinal epithelium every 3–5 days.
- Secrete about 1.8 L of intestinal juice a day (CFTR-dependent Cl⁻ and water).
- Antimicrobial defence (Paneth cells) and mucus production (goblet cells).
- Endocrine signalling.
Clinical significance
Cholera and secretory diarrhoea
Cholera toxin ADP-ribosylates Gsα, which permanently activates adenylate cyclase. The rise in cAMP opens CFTR, causing massive Cl⁻ and water secretion ("rice-water" stools, up to tens of litres a day). Because Na⁺–glucose co-transport (SGLT1) still works, oral rehydration solution is life-saving.
Cystic fibrosis
Defective CFTR leaves the crypt and duct secretions dehydrated and viscous. This causes meconium ileus in newborns, distal intestinal obstruction syndrome and pancreatic insufficiency.
Crypt pathology
Crypt abscesses are typical of ulcerative colitis, and crypt hyperplasia of coeliac disease. Mucositis is the price of the rapid crypt cell division that cytotoxic chemotherapy targets.
Compiled from standard anatomy and physiology references — see the Digestive System sources. For education only; not medical advice.