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GIP
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2L71, 2B4N, 2OBU, 2QKH, 2L70, 1T5Q
Identifiers
Aliases	GIP, gastric inhibitory polypeptide
External IDs	OMIM: 137240; MGI: 107504; HomoloGene: 3043; GeneCards: GIP; OMA:GIP - orthologs
Gene location (Human) Chr. Chromosome 17 (human) Band 17q21.32 Start 48,958,554 bp End 48,968,596 bp
Gene location (Mouse) Chr. Chromosome 11 (mouse) Band 11|11 D Start 95,915,371 bp End 95,921,657 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in jejunal mucosa duodenum gonad testicle buccal mucosa cell pancreatic ductal cell stromal cell of endometrium sural nerve placenta liver Top expressed in duodenum crypt of lieberkuhn of small intestine jejunum intestinal epithelium epithelium of small intestine intestinal villus embryo retinal pigment epithelium morula corneal stroma More reference expression data BioGPS n/a
Gene ontology Molecular function hormone activity protein binding signaling receptor binding Cellular component cytoplasm endoplasmic reticulum lumen extracellular region soma secretory granule lumen extracellular space Biological process response to selenium ion response to amino acid response to organic cyclic compound digestive system development regulation of insulin secretion adult locomotory behavior female pregnancy response to peptide hormone positive regulation of cAMP-mediated signaling memory response to glucose response to lipid response to nutrient levels positive regulation of synaptic transmission exploration behavior response to axon injury response to starvation sensory perception of pain positive regulation of glucagon secretion positive regulation of glucose transmembrane transport response to carbohydrate triglyceride homeostasis signal transduction response to acidic pH endocrine pancreas development positive regulation of insulin secretion long-term potentiation regulation of signaling receptor activity G protein-coupled receptor signaling pathway regulation of fatty acid biosynthetic process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 2695 14607 Ensembl ENSG00000159224 ENSMUSG00000014351 UniProt P09681 P48756 RefSeq (mRNA) NM_004123 NM_008119 RefSeq (protein) NP_004114 NP_032145 Location (UCSC) Chr 17: 48.96 – 48.97 Mb Chr 11: 95.92 – 95.92 Mb PubMed search
Wikidata
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Gastric inhibitory polypeptide (GIP), also known as glucose-dependent insulinotropic polypeptide, is an inhibiting hormone of the secretin family of hormones. While it is a weak inhibitor of gastric acid secretion, its main role, being an incretin, is to stimulate insulin secretion.

GIP, along with glucagon-like peptide-1 (GLP-1), belongs to a class of molecules referred to as incretins, which stimulate insulin release on oral food intake.

Synthesis and transport

GIP is derived from a 153-amino acid proprotein encoded by the GIP gene and circulates as a biologically active 42-amino acid peptide. It is synthesized by K cells, which are found in the mucosa of the duodenum and the jejunum of the gastrointestinal tract.

Like all endocrine hormones, it is transported by blood.

Gastric inhibitory polypeptide receptors are seven-transmembrane proteins (GPCRs) found on beta-cells in the pancreas.

Functions

It has traditionally been named gastrointestinal inhibitory peptide or gastric inhibitory peptide and was found to decrease the secretion of stomach acid to protect the small intestine from acid damage, reduce the rate at which food is transferred through the stomach, and inhibit the GI motility and secretion of acid. However, this is incorrect, as it was discovered that these effects are achieved only with higher-than-normal physiological level, and that these results naturally occur in the body through a similar hormone, secretin.

It is now believed that the function of GIP is to induce insulin secretion, which is stimulated primarily by hyperosmolarity of glucose in the duodenum. After this discovery, some researchers prefer the new name of glucose-dependent insulinotropic peptide, while retaining the acronym "GIP." The amount of insulin secreted is greater when glucose is administered orally than intravenously.

In addition to its role as an incretin, GIP is known to inhibit apoptosis of the pancreatic beta cells and to promote their proliferation. It also stimulates glucagon secretion and fat accumulation. GIP receptors are expressed in many organs and tissues including the central nervous system enabling GIP to influence hippocampal memory formation and regulation of appetite and satiety.

GIP recently appeared as a major player in bone remodeling. Researchers at Universities of Angers and Ulster evidenced that genetic ablation of the GIP receptor in mice resulted in profound alterations of bone microarchitecture through modification of the adipokine network. Furthermore, the deficiency in GIP receptors has also been associated in mice with a dramatic decrease in bone quality and a subsequent increase in fracture risk. However, the results obtained by these groups are far from conclusive because their animal models give discordant answers and these works should be analysed very carefully.

Pathology

It has been found that type 2 diabetics are not responsive to GIP and have lower levels of GIP secretion after a meal when compared to non-diabetics. In research involving knockout mice, it was found that absence of the GIP receptors correlates with resistance to obesity.

References

1. ^ GRCh38: Ensembl release 89: ENSG00000159224 – Ensembl, May 2017
2. ^ GRCm38: Ensembl release 89: ENSMUSG00000014351 – Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Meier JJ, Nauck MA (2005). "Glucagon-like peptide 1(GLP-1) in biology and pathology". Diabetes/Metabolism Research and Reviews. 21 (2): 91–117. doi:10.1002/dmrr.538. PMID 15759282. S2CID 39547553.
6. Pederson RA, McIntosh CH (2016). "Discovery of gastric inhibitory polypeptide and its subsequent fate: Personal reflections". Journal of Diabetes Investigation. 7 (Suppl 1): 4–7. doi:10.1111/jdi.12480. PMC 4854497. PMID 27186348.
7. Efendic S, Portwood N (2004). "Overview of incretin hormones". Hormone and Metabolic Research. 36 (11–12): 742–6. doi:10.1055/s-2004-826157. PMID 15655702. S2CID 11634548.
8. Costanzo L (2014). Physiology. Philadelphia, PA: Saunders/Elsevier. p. 337. ISBN 9781455708475.
9. Kim W, Egan JM (Dec 2008). "The role of incretins in glucose homeostasis and diabetes treatment". Pharmacological Reviews. 60 (4): 470–512. doi:10.1124/pr.108.000604. PMC 2696340. PMID 19074620.
10. Creutzfeldt W, Ebert R, Ørskov C, Bartels E, Nauck MA (1992). "Lack of Effect of Synthetic Human Gastric Inhibitory Polypeptide and Glucagon-LikePeptide 1 [7-36 Amide] Infused at Near-Physiological Concentrations on Pentagastrin-Stimulated Gastric Acid Secretion in Normal Human Subjects". Digestion. 52 (3–4): 214–221. doi:10.1159/000200956. ISSN 0012-2823. PMID 1459356.
11. Thorens B (Dec 1995). "Glucagon-like peptide-1 and control of insulin secretion". Diabète & Métabolisme. 21 (5): 311–8. PMID 8586147.
12. Boron WF, Boulpaep EL (2009). Medical physiology: a cellular and molecular approach (2nd International ed.). Philadelphia, PA: Saunders/Elsevier. ISBN 9781416031154.
13. Seino Y, Fukushima M, Yabe D (2010). "GIP and GLP-1, the two incretin hormones: Similarities and differences". Journal of Diabetes Investigation. 1 (1–2): 8–23. doi:10.1111/j.2040-1124.2010.00022.x. PMC 4020673. PMID 24843404.
14. Gaudin-Audrain C, Irwin N, Mansur S, Flatt PR, Thorens B, Baslé M, Chappard D, Mabilleau G (Mar 2013). "Glucose-dependent insulinotropic polypeptide receptor deficiency leads to modifications of trabecular bone volume and quality in mice" (PDF). Bone. 53 (1): 221–30. doi:10.1016/j.bone.2012.11.039. PMID 23220186. S2CID 36280105. Archived from the original (PDF) on 2018-07-21. Retrieved 2018-11-20.
15. Mieczkowska A, Irwin N, Flatt PR, Chappard D, Mabilleau G (Oct 2013). "Glucose-dependent insulinotropic polypeptide (GIP) receptor deletion leads to reduced bone strength and quality" (PDF). Bone. 56 (2): 337–42. doi:10.1016/j.bone.2013.07.003. PMID 23851294. S2CID 19296511.
16. Skrha J, Hilgertová J, Jarolímková M, Kunešová M, Hill M (2010). "Meal test for glucose-dependent insulinotropic peptide (GIP) in obese and type 2 diabetic patients". Physiological Research. 59 (5): 749–55. doi:10.33549/physiolres.931893. PMID 20406045.
17. Yamada Y, Seino Y (2004). "Physiology of GIP--a lesson from GIP receptor knockout mice". Hormone and Metabolic Research. 36 (11–12): 771–4. doi:10.1055/s-2004-826162. PMID 15655707. S2CID 262453421.

External links

• Gastric+inhibitory+polypeptide at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
• King MW (16 November 2006). "Gastrointestinal Hormones and Peptides". Indiana University – Purdue University Indianapolis School of Medicine. Archived from the original on 6 December 2007. Retrieved 1 October 2006.
• Overview of all the structural information available in the PDB for UniProt: P09681 (Gastric inhibitory polypeptide) at the PDBe-KB.

• Genes on human chromosome 17
• Gastroenterology
• Intestinal hormones
• Diabetes