The ups and downs of growth hormone secretagogue receptor signaling. (2nd March 2021)
- Record Type:
- Journal Article
- Title:
- The ups and downs of growth hormone secretagogue receptor signaling. (2nd March 2021)
- Main Title:
- The ups and downs of growth hormone secretagogue receptor signaling
- Authors:
- Cornejo, María P.
Mustafá, Emilio R.
Cassano, Daniela
Banères, Jean‐Louis
Raingo, Jesica
Perello, Mario - Abstract:
- Abstract : The growth hormone secretagogue receptor (GHSR) has emerged as one of the most fascinating molecules from the perspective of neuroendocrine control. GHSR is mainly expressed in the pituitary and the brain, and plays key roles regulating not only growth hormone secretion but also food intake, adiposity, body weight, glucose homeostasis and other complex functions. Quite atypically, GHSR signaling displays a basal constitutive activity that can be up‐ or downregulated by two digestive system‐derived hormones: the octanoylated‐peptide ghrelin and the liver‐expressed antimicrobial peptide 2 (LEAP2), which was recently recognized as an endogenous GHSR ligand. The existence of two ligands with contrary actions indicates that GHSR activity can be tightly regulated and that the receptor displays the capability to integrate such opposing inputs in order to provide a balanced intracellular signal. This article provides a summary of the current understanding of the biology of ghrelin, LEAP2 and GHSR and discusses the reconceptualization of the cellular and physiological implications of the ligand‐regulated GHSR signaling, based on the latest findings. Abstract : The growth hormone secretagogue receptor (GHSR) is a fascinating molecule that controls numerous neuroendocrine functions and behaviors. GHSR activity is up‐ and downregulated by two digestive system‐derived peptides, ghrelin and liver‐expressed antimicrobial peptide 2 (LEAP2), respectively, that, in turn, integrateAbstract : The growth hormone secretagogue receptor (GHSR) has emerged as one of the most fascinating molecules from the perspective of neuroendocrine control. GHSR is mainly expressed in the pituitary and the brain, and plays key roles regulating not only growth hormone secretion but also food intake, adiposity, body weight, glucose homeostasis and other complex functions. Quite atypically, GHSR signaling displays a basal constitutive activity that can be up‐ or downregulated by two digestive system‐derived hormones: the octanoylated‐peptide ghrelin and the liver‐expressed antimicrobial peptide 2 (LEAP2), which was recently recognized as an endogenous GHSR ligand. The existence of two ligands with contrary actions indicates that GHSR activity can be tightly regulated and that the receptor displays the capability to integrate such opposing inputs in order to provide a balanced intracellular signal. This article provides a summary of the current understanding of the biology of ghrelin, LEAP2 and GHSR and discusses the reconceptualization of the cellular and physiological implications of the ligand‐regulated GHSR signaling, based on the latest findings. Abstract : The growth hormone secretagogue receptor (GHSR) is a fascinating molecule that controls numerous neuroendocrine functions and behaviors. GHSR activity is up‐ and downregulated by two digestive system‐derived peptides, ghrelin and liver‐expressed antimicrobial peptide 2 (LEAP2), respectively, that, in turn, integrate different types of metabolic, autonomic, and endocrine signals. This article summarizes the biology of ghrelin, LEAP2 and GHSR and discusses the cellular and physiological implications of GHSR signaling. … (more)
- Is Part Of:
- FEBS journal. Volume 288:Number 24(2021)
- Journal:
- FEBS journal
- Issue:
- Volume 288:Number 24(2021)
- Issue Display:
- Volume 288, Issue 24 (2021)
- Year:
- 2021
- Volume:
- 288
- Issue:
- 24
- Issue Sort Value:
- 2021-0288-0024-0000
- Page Start:
- 7213
- Page End:
- 7229
- Publication Date:
- 2021-03-02
- Subjects:
- food intake regulation -- ghrelin -- GHSR -- glucose homeostasis -- LEAP2
Biochemistry -- Periodicals
Molecular biology -- Periodicals
Pathology, Molecular -- Periodicals
572 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=01038983-000000000-00000 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=ejb ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=ejb ↗ - DOI:
- 10.1111/febs.15718 ↗
- Languages:
- English
- ISSNs:
- 1742-464X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3901.578500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26853.xml