PUBLICATION

Secretoneurin is a secretogranin-2 derived hormonal peptide in vertebrate neuroendocrine systems

Authors
Mitchell, K., Mikwar, M., Da Fonte, D., Lu, C., Tao, B., Peng, D., Udeesha Erandani, W.K.C., Hu, W., Trudeau, V.L.
ID
ZDB-PUB-200825-3
Date
2020
Source
General and comparative endocrinology   299: 113588 (Journal)
Registered Authors
Trudeau, V.L.
Keywords
feeding, gonadotropin-releasing hormone, hypothalamus, neurogenesis, neuroinflammation, neuropeptide, pituitary, reproduction, secretogranin-2, secretoneurin
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Female
  • Goldfish
  • Humans
  • Male
  • Mice
  • Neuropeptides/metabolism*
  • Secretogranin II/metabolism*
  • Zebrafish
PubMed
32828813 Full text @ Gen. Comp. Endocrinol.
Abstract
Secretogranin-2 (SCG2) is a granin-derived precursor protein that is processed into several potentially bioactive peptides, with the 30-43 amino acid central domain called secretoneurin (SN) being clearly evolutionary conserved in vertebrates. Secretoneurin exerts a diverse array of biological functions including regulating nervous, endocrine, and immune systems in part due to its wide tissue distribution. Expressed in some neuroendocrine neurons and pituitary cells, SN is a stimulator of the synthesis and release of luteinizing hormone from both goldfish pituitary cells and the mouse LβT2 cell line. Neuroendocrine, paracrine and autocrine signaling pathways for the regulation of luteinizing hormone release indicate hormone-like activities to regulate reproduction. Mutation of the scg2a and scg2b genes using TALENs in zebrafish reduces sexual behavior, ovulation, oviposition, and fertility. A single injection of the SNa peptide enhanced reproductive outcomes in scg2a/scg2b double mutant zebrafish fish. Evidence in goldfish suggests a new role for SN to stimulate food intake by actions on other feeding-related neuropeptides. Expression and regulation of the Scg2a precursor mRNA in goldfish gut also supports a role in feeding. In rodent models, SN has trophic-like properties promoting both neuroprotection and neuronal plasticity and has chemoattractant properties that regulate neuroinflammation. Data obtained from several cellular models suggest that SN binds to and activates a G-protein coupled receptor (GPCR), but a bona fide SN receptor protein needs to be identified. Other signaling pathways for SN have been reported which provides alternatives to the GPCR hypothesis. These include AMP-activated protein kinase (AMPK), extracellular signal-regulated kinases (ERK), mitogen-activated protein kinase (MAPK)and calcium/calmodulin-dependent protein kinase II in cardiomyocytes, phosphatidylinositol 3-kinase (PI3K) and Akt/Protein Kinase B (AKT, and MAPK in endothelial cells and Janus kinase 2/signal transducer and activator of transcription protein (JAK2-STAT) signaling in neurons. Some studies in cardiac cells provide evidence for cellular internalization of SN by an unknown mechanism. Many of the biological functions of SN remain to be fully characterized, which could lead to new and exciting applications.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping