TY - JOUR
T1 - Cranial Suture Regeneration Mitigates Skull and Neurocognitive Defects in Craniosynostosis
AU - Yu, Mengfei
AU - Ma, Li
AU - Yuan, Yuan
AU - Ye, Xin
AU - Montagne, Axel
AU - He, Jinzhi
AU - Ho, Thach-Vu
AU - Wu, Yingxi
AU - Zhao, Zhen
AU - Sta Maria, Naomi
AU - Jacobs, Russell
AU - Urata, Mark
AU - Wang, Huiming
AU - Zlokovic, Berislav V
AU - Chen, Jian-Fu
AU - Chai, Yang
N1 - Copyright © 2020 Elsevier Inc. All rights reserved.
PY - 2021/1/7
Y1 - 2021/1/7
N2 - 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.
AB - 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.
U2 - 10.1016/j.cell.2020.11.037
DO - 10.1016/j.cell.2020.11.037
M3 - Article
C2 - 33417861
SN - 0092-8674
VL - 184
SP - 243-256.e18
JO - Cell
JF - Cell
IS - 1
ER -