| Literature DB >> 33417861 |
Mengfei Yu1, Li Ma2, Yuan Yuan2, Xin Ye3, Axel Montagne4, Jinzhi He2, Thach-Vu Ho2, Yingxi Wu4, Zhen Zhao4, Naomi Sta Maria4, Russell Jacobs4, Mark Urata5, Huiming Wang3, Berislav V Zlokovic4, Jian-Fu Chen2, Yang Chai6.
Abstract
Craniosynostosis results from premature fusion of the cranial suture(s), which contain mesenchymal stem cells (MSCs) that are crucial for calvarial expansion in coordination with brain growth. Infants with craniosynostosis have skull dysmorphology, increased intracranial pressure, and complications such as neurocognitive impairment that compromise quality of life. Animal models recapitulating these phenotypes are lacking, hampering development of urgently needed innovative therapies. Here, we show that Twist1+/- mice with craniosynostosis have increased intracranial pressure and neurocognitive behavioral abnormalities, recapitulating features of human Saethre-Chotzen syndrome. Using a biodegradable material combined with MSCs, we successfully regenerated a functional cranial suture that corrects skull deformity, normalizes intracranial pressure, and rescues neurocognitive behavior deficits. The regenerated suture creates a niche into which endogenous MSCs migrated, sustaining calvarial bone homeostasis and repair. MSC-based cranial suture regeneration offers a paradigm shift in treatment to reverse skull and neurocognitive abnormalities in this devastating disease.Entities:
Keywords: Twist1; calvarial deformity; mesenchymal stem cells; neurocognitive abnormalities; suture regeneration
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Year: 2021 PMID: 33417861 PMCID: PMC7891303 DOI: 10.1016/j.cell.2020.11.037
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 66.850