Liu Xiao, Xie Furong, Lai Guangyun, Wang Jun
Department of Pediatric Dentistry, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine, China; National Clinical Research Center for Oral Diseases, China; Shanghai Key Laboratory of Stomatology and Shanghai Research Institute of Stomatology, Shanghai, 200011, China.
Department of Pediatric Dentistry, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine, China; National Clinical Research Center for Oral Diseases, China; Shanghai Key Laboratory of Stomatology and Shanghai Research Institute of Stomatology, Shanghai, 200011, China.
Arch Oral Biol. 2020 Dec;120:104933. doi: 10.1016/j.archoralbio.2020.104933. Epub 2020 Oct 7.
We aimed to explore the role of Heterogeneous Nuclear Ribonucleoprotein L(hnRNP L) in enamel organ development through hnRNP L conditional knockout mice and knockdown of hnRNP L expression in mouse ameloblast-lineage cells (mALCs) METHODS: We created K14cre-mediated hnRNP L conditional knockout mice (hnRNP L) and silenced the expression of hnRNP L in mALCs to investigate the role of hnRNP L in enamel organ development.
We found that hnRNP L mice presented enamel organ development defects with reduced number of inner enamel epithelium (IEE) cells. The proliferation and differentiation of the IEE cells/ameloblasts were suppressed. The cell proliferation and mineralization ability were also decreased after hnRNP L knockdown. Further studies showed that Bone Morphogenetic Protein (BMP) signaling pathway was attenuated after the knockdown of hnRNP L expression both in vivo and in vitro.
These findings suggest that hnRNP L plays a critical role in enamel organ development by promoting the IEE cell/ameloblast proliferation and differentiation. BMP signaling pathway may be involved in the process.
我们旨在通过hnRNP L条件性敲除小鼠以及敲低小鼠成釉细胞系细胞(mALCs)中hnRNP L的表达,来探究不均一核核糖核蛋白L(hnRNP L)在釉器发育中的作用。方法:我们构建了K14cre介导的hnRNP L条件性敲除小鼠(hnRNP L),并使mALCs中hnRNP L的表达沉默,以研究hnRNP L在釉器发育中的作用。
我们发现hnRNP L小鼠出现釉器发育缺陷,内釉上皮(IEE)细胞数量减少。IEE细胞/成釉细胞的增殖和分化受到抑制。敲低hnRNP L后,细胞增殖和矿化能力也降低。进一步研究表明,在体内和体外敲低hnRNP L表达后,骨形态发生蛋白(BMP)信号通路均被减弱。
这些发现表明,hnRNP L通过促进IEE细胞/成釉细胞的增殖和分化,在釉器发育中起关键作用。BMP信号通路可能参与了这一过程。