Developmental activities of the complement pathway in migrating neurons.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28462915.
- Also identified by DOI 10.1038/ncomms15096 and PMC identifier 5418580.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
In recent years the notion that malfunctioning of the immune system may result in developmental brain diseases has emerged. However, the role of immune molecules in the developing brain has not been well explored. The complement pathway converges to cleave C3. Here we show that key proteins in the lectin arm of this pathway, MASP1, MASP2 and C3, are expressed in the developing cortex and that neuronal migration is impaired in knockout and knockdown mice. Molecular mimics of C3 cleavage products rescue the migration defects that have been seen following knockdown of C3 or Masp2. Pharmacological activation of the downstream receptors rescue Masp2 and C3 knockdown as well as C3 knockout. Therefore, we propose that the complement pathway is functionally important in migrating neurons of the developing cortex.
Medical subject headings
- Complement C3
- Complement Pathway, Mannose-Binding Lectin
- Gene Expression Regulation, Developmental
- Mannose-Binding Protein-Associated Serine Proteases
- Neurons