Search bioRxiv⌕ Search

Biology subjects

Rodriguez-Navarro, I.

Publications and source records attributed to Rodriguez-Navarro, I..

2 recordsLinked to original sources

LRRTM4 controls cell migration via Glypican interactions

Leucine-rich-repeat-transmembrane neuronal proteins (LRRTMs) play a major role in neuronal connectivity and synapse formation, but their function during early development remains largely unexplored and roles in cell migration have not been described. Here, we identify LRRTM4 as a major coordinator of cell migration within the developing cortex and in cancer cells. Using structural predictions and site-directed mutagenesis to abolish the LRRTM4-glypican interaction, we show that LRRTMs interact with the core domain of glypicans, which, in the midgestational murine cortex, are presented by radial glia cells. We demonstrate that glypican-bound LRRTM4 mediates contact-repulsion in migrating neurons and cancer cells in vitro. Our results demonstrate that LRRTMs are used by migrating cells responding to glypicans, and that this signaling system is active in migrating cancer cells and during development.

developmental biology↗

A double hit affecting the IKZF1-IKZF2 tandem in immune cells of schizophrenic patients regulate specific symptoms

Schizophrenia is a complex multifactorial disorder and increasing evidence suggests the involvement of immune dysregulations in its pathogenesis. We observed that IKZF1 and IKZF2, classic immune-related transcription factors (TFs), were both downregulated in patients peripheral blood mononuclear cells (PBMCs) but not in their brain. We generated a new mutant mouse model with a reduction in Ikzf1 and Ikzf2 to study the impact of those changes. Such mice developed deficits in the three dimensions (positive-negative-cognitive) of schizophrenic-like phenotypes associated with alterations in structural synaptic plasticity. We then studied the secretomes of cultured PBMCs obtained from human patients and identified potentially secreted molecules, which depended on IKZF1 and IKZF2 levels, and that in turn have an impact on neural synchrony, structural synaptic plasticity and schizophrenic-like symptoms in in vivo and in vitro models. Our results point out that IKZF1-IKZF2-dependent immune signals negatively impact on essential neural circuits involved in schizophrenia.

neuroscience↗