Journal Article

Neural EGFL-like 1, a craniosynostosis-related osteochondrogenic molecule, strikingly associates with neurodevelopmental pathologies

Jiang, Wenlu, Ting, Kang, Li, Chenshuang, Ha, Pin, Soo, Chia, Zheng, Zhong

2023

Overview

Various craniofacial syndromes cause skeletal malformations and are accompanied by neurological abnormalities at different levels, leading to tremendous biomedical, financial, social, and psychological burdens. Accumulating evidence highlights the importance of identifying and characterizing the genetic basis that synchronously modulates musculoskeletal and neurobehavioral development and function. Particularly, previous studies from different groups have suggested that neural EGFL-like-1 (Nell-1), a well-established osteochondrogenic inducer whose biopotency was initially identified in the craniofacial tissues, may also play a vital role in the central nervous system, particularly regarding neurological disorder pathologies. To provide first-hand behavior evidence if Nell-1 also has a role in central nervous system abnormalities, we compared the Nell-1-haploinsufficient ( Nell-1 +/6R ) mice with their wild-type counterparts regarding their repetitive, social communication, anxiety-related, locomotor, sensory processing-related, motor coordination, and Pavlovian learning and memory behaviors, as well as their hippocampus transcriptional profile. Interestingly, Nell-1 +/6R mice demonstrated core autism spectrum disorder-like deficits, which could be corrected by Risperidone, an FDA-approved anti-autism, anti-bipolar medicine. Besides, transcriptomic analyses identified 269 differential expressed genes, as well as significantly shifted alternative splicing of ubiquitin B pseudogene Gm1821 , in the Nell-1 +/6R mouse hippocampus, which confirmed that Nell-1 plays a role in neurodevelopment. Therefore, the current study verifies that Nell-1 regulates neurological development and function for the first time. Moreover, this study opens new avenues for understanding and treating craniofacial patients suffering from skeletal deformities and behavior, memory, and cognition difficulties by uncovering a novel bone-brain-crosstalk network. Furthermore, the transcriptomic analysis provides the first insight into deciphering the mechanism of Nell-1 in neurodevelopment.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Abnormalities / Alternative splicing / Autism / Autism spectrum disorder / Behavior / Biomedical and Life Sciences / Birth defects / Bone-brain-crosstalk / Cell Biology / Central nervous system / Cognition / Craniofacial syndromes / Craniosynostosis / Disability / Enzymes / Females / Genes / Hair loss / Hippocampus / Information processing / Letter to the Editor / Life Sciences / Memory / Microbiology / Motor skill learning / Nervous system / Nervous system diseases / Neural EGFL-like 1 / Neurobiology / Neurodevelopment / Neurodevelopmental / Proteomics / Risperidone / Sensory integration / Social interaction / Stem Cells / Transcriptomics / Ubiquitin