Park Sarah S, Beyer Richard P, Smyth Matthew D, Clarke Christine M, Timms Andrew E, Bammler Theo K, Stamper Brendan D, Mecham Brigham H, Gustafson Jennifer A, Cunningham Michael L
Seattle Children's Research Institute, Center for Developmental Biology and Regenerative Medicine, Seattle, WA, USA.
University of Washington, Center for Ecogenetics and Environmental Health, Seattle, WA, USA.
Bone. 2015 Jul;76:169-76. doi: 10.1016/j.bone.2015.03.001. Epub 2015 Mar 7.
Single suture craniosynostosis (SSC) is the premature fusion of one calvarial suture and occurs in 1-1700-2500 live births. Congenital fusion of either the sagittal, metopic, or coronal sutures represents 95% of all cases of SSC. Sagittal and metopic synostosis have a male preponderance (3:1) while premature fusion of the coronal suture has a female preponderance (2:1). Although environmental and genetic factors contribute to SSC, the etiology of the majority of SSC cases remains unclear. In this study, 227 primary calvarial osteoblast cell lines from patients with coronal, metopic, or sagittal synostosis and unaffected controls were established and assayed for ALP activity and BrdU incorporation (n = 226) as respective measures of early stage osteoblast differentiation and proliferation. Primary osteoblast cell lines from individuals with sagittal synostosis demonstrated higher levels of ALP activity and reduced proliferation when compared to control lines. In order to address the sex differences in SSC types, the data was further stratified by sex. Osteoblasts from males and females with sagittal synostosis as well as males with metopic synostosis demonstrated higher levels of ALP activity when compared to sex matched controls, and males with sagittal or metopic synostosis demonstrated reduced levels of proliferation. In order to elucidate genes and pathways involved in these observed phenotypes, correlation analyses comparing ALP activity and proliferation to global gene expression was performed. Transcripts related to osteoblast differentiation were identified both differentially up and downregulated, correlated with ALP activity when compared to controls, and demonstrated a striking sex specific gene expression pattern. These data support that the dysregulation of osteoblast differentiation plays a role in the development of SSC and that genetic factors contribute to the observed sex related differences.
单缝颅缝早闭(SSC)是指一条颅骨缝过早融合,在1 - 1700 - 2500例活产婴儿中发生。矢状缝、额缝或冠状缝的先天性融合占所有SSC病例的95%。矢状缝和额缝早闭以男性居多(3:1),而冠状缝过早融合则以女性居多(2:1)。尽管环境和遗传因素都与SSC有关,但大多数SSC病例的病因仍不清楚。在本研究中,建立了来自冠状缝、额缝或矢状缝早闭患者及未受影响对照的227个原代颅骨成骨细胞系,并检测了碱性磷酸酶(ALP)活性和5-溴脱氧尿嘧啶核苷(BrdU)掺入情况(n = 226),分别作为早期成骨细胞分化和增殖的指标。与对照系相比,来自矢状缝早闭个体的原代成骨细胞系表现出更高水平的ALP活性和增殖减少。为了解决SSC类型中的性别差异问题,数据按性别进一步分层。与性别匹配的对照相比,患有矢状缝早闭的男性和女性以及患有额缝早闭的男性的成骨细胞表现出更高水平的ALP活性,而患有矢状缝或额缝早闭的男性表现出增殖水平降低。为了阐明参与这些观察到的表型的基因和途径,进行了将ALP活性和增殖与全基因组表达进行比较的相关性分析。与成骨细胞分化相关的转录本被鉴定为差异上调和下调,与对照相比与ALP活性相关,并表现出显著的性别特异性基因表达模式。这些数据支持成骨细胞分化失调在SSC的发生中起作用,并且遗传因素导致了观察到的性别相关差异。