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Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties

Authors :
Stefka Mincheva-Tasheva
Chandran Pfitzner
Raman Kumar
Idha Kurtsdotter
Michaela Scherer
Tarin Ritchie
Jonas Muhr
Jozef Gecz
Paul Q. Thomas
Source :
Open Biology, Vol 14, Iss 4 (2024)
Publication Year :
2024
Publisher :
The Royal Society, 2024.

Abstract

Non-clustered protocadherins (ncPcdhs) are adhesive molecules with spatio-temporally regulated overlapping expression in the developing nervous system. Although their unique role in neurogenesis has been widely studied, their combinatorial role in brain physiology and pathology is poorly understood. Using probabilistic cell typing by in situ sequencing, we demonstrate combinatorial inter- and intra-familial expression of ncPcdhs in the developing mouse cortex and hippocampus, at single-cell resolution. We discovered the combinatorial expression of Protocadherin-19 (Pcdh19), a protein involved in PCDH19-clustering epilepsy, with Pcdh1, Pcdh9 or Cadherin 13 (Cdh13) in excitatory neurons. Using aggregation assays, we demonstrate a code-specific adhesion function of PCDH19; mosaic PCDH19 absence in PCDH19+9 and PCDH19 + CDH13, but not in PCDH19+1 codes, alters cell–cell interaction. Interestingly, we found that PCDH19 as a dominant protein in two heterophilic adhesion codes could promote trans-interaction between them. In addition, we discovered increased CDH13-mediated cell adhesion in the presence of PCDH19, suggesting a potential role of PCDH19 as an adhesion mediator of CDH13. Finally, we demonstrated novel cis-interactions between PCDH19 and PCDH1, PCDH9 and CDH13. These observations suggest that there is a unique combinatorial code with a cell- and region-specific characteristic where a single molecule defines the heterophilic cell–cell adhesion properties of each code.

Details

Language :
English
ISSN :
20462441
Volume :
14
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Open Biology
Publication Type :
Academic Journal
Accession number :
edsdoj.1be471afb0de4b3196a50568149a88fa
Document Type :
article
Full Text :
https://doi.org/10.1098/rsob.230383