Spatiotemporal expression profiles of c-Mpl mRNA in the tooth germ: Comparative expression dynamics of vascularization-related genes

IF 2 3区 医学 Q2 ANATOMY & MORPHOLOGY
Masataka Sunohara , Shigeru Morikawa , Kazuto Shimada , Kingo Suzuki
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Abstract

Background

Vascularization is an essential event for both embryonic organ development and tissue repair in adults. During mouse tooth development, endothelial cells migrate into dental papilla during the cap stage, and form blood vessels through angiogenesis. Megakaryocytes and/or platelets, as other hematopoietic cells, express angiogenic molecules and can promote angiogenesis in adult tissues. However, it remains unknown which cells are responsible for attracting and leading blood vessels through the dental papilla during tooth development.

Methods

Here we analyzed the spatiotemporal expression of c-Mpl mRNA in developing molar teeth of fetal mice. Expression patterns were then compared with those of several markers of hematopoietic cells as well as of angiogenic elements including CD41, erythropoietin receptor, CD34, angiopoietin-1 (Ang-1), Tie-2, and vascular endothelial growth factor receptor2 (VEGFR2) through in situ hybridization or immunohistochemistry.

Results

Cells expressing c-Mpl mRNA was found in several parts of the developing tooth germ, including the peridental mesenchyme, dental papilla, enamel organ, and dental lamina. This expression occurred in a spatiotemporally controlled fashion. CD41-expressing cells were not detected during tooth development. The spatiotemporal expression pattern of c-Mpl mRNA in the dental papilla was similar to that of Ang-1, which preceded invasion of endothelial cells. Eventually, at the early bell stage, the c-Mpl mRNA signal was detected in morphologically differentiating odontoblasts that accumulated in the periphery of the dental papilla along the inner enamel epithelium layer of the future cusp region.

Conclusion

During tooth development, several kinds of cells express c-Mpl mRNA in a spatiotemporally controlled fashion, including differentiating odontoblasts. We hypothesize that c-Mpl-expressing cells appearing in the forming dental papilla at the cap stage are odontoblast progenitor cells that migrate to the site of odontoblast differentiation. There they attract vascular endothelial cells into the forming dental papilla and lead cells toward the inner enamel epithelium layer through production of angiogenic molecules (e.g., Ang-1) during migration to the site of differentiation. C-Mpl may regulate apoptosis and/or proliferation of expressing cells in order to execute normal development of the tooth.

牙胚中 c-Mpl mRNA 的时空表达谱:血管形成相关基因的比较表达动态。
背景:血管形成是胚胎器官发育和成人组织修复的重要环节。在小鼠牙齿发育过程中,内皮细胞在牙帽期迁移到牙乳头,并通过血管生成形成血管。巨核细胞和/或血小板与其他造血细胞一样,表达血管生成分子,可促进成人组织的血管生成。方法:在此,我们分析了c-Mpl mRNA在胎鼠臼齿发育过程中的时空表达。然后通过原位杂交或免疫组织化学方法,将 c-Mpl mRNA 的表达模式与几种造血细胞和血管生成因子标记物(包括 CD41、红细胞生成素受体、CD34、血管生成素-1(Ang-1)、Tie-2 和血管内皮生长因子受体 2(VEGFR2))的表达模式进行比较:结果:在发育中的牙胚的多个部位都发现了表达 c-Mpl mRNA 的细胞,包括牙周间质、牙乳头、釉质器官和牙层。这种表达是以时空控制的方式出现的。在牙齿发育过程中未检测到表达 CD41 的细胞。c-Mpl mRNA在牙乳头的时空表达模式与Ang-1相似,后者先于内皮细胞入侵。最终,在早期钟期,c-Mpl mRNA信号在形态分化的牙本质细胞中被检测到,这些牙本质细胞沿着未来尖突区域的内釉上皮层聚集在牙乳头的外围:结论:在牙齿发育过程中,多种细胞以时空可控的方式表达c-Mpl mRNA,包括正在分化的牙本质细胞。我们推测,在牙帽期出现在成形牙乳头中的c-Mpl表达细胞是迁移到牙本质分化部位的牙本质祖细胞。在那里,它们吸引血管内皮细胞进入形成中的牙乳头,并在向分化部位迁移的过程中通过产生血管生成分子(如 Ang-1)将细胞引向内釉上皮层。C-Mpl 可调节表达细胞的凋亡和/或增殖,以保证牙齿的正常发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Anatomy-Anatomischer Anzeiger
Annals of Anatomy-Anatomischer Anzeiger 医学-解剖学与形态学
CiteScore
4.40
自引率
22.70%
发文量
137
审稿时长
33 days
期刊介绍: Annals of Anatomy publish peer reviewed original articles as well as brief review articles. The journal is open to original papers covering a link between anatomy and areas such as •molecular biology, •cell biology •reproductive biology •immunobiology •developmental biology, neurobiology •embryology as well as •neuroanatomy •neuroimmunology •clinical anatomy •comparative anatomy •modern imaging techniques •evolution, and especially also •aging
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