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reelin
ProteinQ13561329· pop 22· linked from 215 articles

Also known as uniprot:P78509, RELN

Reelin, encoded by the RELN gene, is a large secreted extracellular matrix glycoprotein that helps regulate processes of neuronal migration and positioning in the developing brain by controlling cell–cell interactions. Besides this important role in early development, reelin continues to work in the adult brain. It modulates synaptic plasticity by enhancing the induction and maintenance of long-term potentiation. It also stimulates dendrite and dendritic spine development in the hippocampus, and regulates the continuing migration of neuroblasts generated in adult neurogenesis sites of the subv

Protein · UniProt

Reelin

Gene
RELN
Organism
Homo sapiens (Human)
Length
3,460 aa
Molecular mass
388,388 Da
Evidence
1: Evidence at protein level

Extracellular matrix serine protease secreted by pioneer neurons that plays a role in layering of neurons in the cerebral cortex and cerebellum by coordinating cell positioning during neurodevelopment. Regulates microtubule function in neurons and neuronal migration. Binding to the extracellular domains of lipoprotein receptors VLDLR and LRP8/APOER2 induces tyrosine phosphorylation of DAB1 and modulation of TAU phosphorylation. Affects migration of sympathetic preganglionic neurons in the spinal cord, where it seems to act as a barrier to neuronal migration. Enzymatic activity is important …

3D-structureAlternative splicingCalciumCell adhesionDevelopmental proteinDisease variantDisulfide bondEGF-like domain
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Swiss-Prot (reviewed) · via UniProt

Wikidata facts

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Commons category
Reelin
EC enzyme number
3.4.21.-
Sources (4)

via Wikidata · CC0

~43 min read

Article

26 sections
Contents
  • Discovery
  • Tissue distribution and secretion
  • Structure
  • Function
  • During development
  • In adults
  • Evolutionary significance
  • Mechanism of action
  • Receptors
  • Signaling cascades
  • Complexes
  • Interaction with Cdk5
  • Possible pathological role
  • Lissencephaly
  • Schizophrenia
  • Bipolar disorder
  • Autism
  • Temporal lobe epilepsy: granule cell dispersion
  • Alzheimer's disease
  • Cancer
  • Other conditions
  • Factors affecting reelin expression
  • Psychotropic medication
  • References
  • Further reading
  • External links

Reelin, encoded by the RELN gene, is a large secreted extracellular matrix glycoprotein that helps regulate processes of neuronal migration and positioning in the developing brain by controlling cell–cell interactions. Besides this important role in early development, reelin continues to work in the adult brain. It modulates synaptic plasticity by enhancing the induction and maintenance of long-term potentiation. It also stimulates dendrite and dendritic spine development in the hippocampus, and regulates the continuing migration of neuroblasts generated in adult neurogenesis sites of the subventricular and subgranular zones. It is found not only in the brain but also in the liver, thyroid gland, adrenal gland, fallopian tube, breast and in comparatively lower levels across a range of anatomical regions.

Reelin has been suggested to be implicated in pathogenesis of several brain diseases. The expression of the protein has been found to be significantly lower in schizophrenia and psychotic bipolar disorder, but the cause of this observation remains uncertain, as studies show that psychotropic medication itself affects reelin expression. Moreover, epigenetic hypotheses aimed at explaining the changed levels of reelin expression are controversial. Total lack of reelin causes a form of lissencephaly. Reelin may also play a role in Alzheimer's disease, temporal lobe epilepsy and autism.

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