Institute of Special Wild Economic Animals and Plants, Chinese Academy of Agricultural Sciences, 4899 Juye Street, Changchun, 130112, China.
AgResearch Ltd, Ruakura Agricultural Centre, 10 Bisley Road, Hamilton, 3214, New Zealand.
Cell Death Dis. 2019 Jun 5;10(6):443. doi: 10.1038/s41419-019-1686-y.
Deer antlers are extraordinary mammalian organs that can fully regenerate annually. Antler renewal is a stem cell-based epimorphic process and antler stem (AS) cells can initiate de novo generation of antlers in postnatal mammals. However, although being called stem cells, the AS cells have not been characterized at molecular level based on the stem cell criteria. Comprehensive characterization of the AS cells would undoubtedly help to decipher the mechanism underlying the full regeneration of deer antlers, the only case of stem cell-based epimorphic regeneration in mammals. In the present study, three types of AS cells (antlerogenic periosteal cells APCs, for initial pedicle and first antler formation; pedicle periosteal cells PPC, for annual antler regeneration; and reserve mesenchyme cells RMCs, for rapid antler growth), were isolated for comprehensive molecular characterization. A horn-growth-related gene, RXFP2, was found to be expressed only in AS cells lineages but not in the facial periosteal cells (FPCs, locates geographically in the vicinity of the APCs or PPCs), suggesting the RXFP2 might be a specific marker for the AS cell lineage in deer. Our results demonstrated that AS cells expressed classic MSC markers including surface markers CD73, CD90, CD105 and Stro-1. They also expressed some of the markers including Tert, Nestin, S100A4, nucleostemin and C-Myc, suggesting that they have some attributes of the ESCs. Microinjection of male APC into deer blastocysts resulted in one female foetus (110 days gestation) recovered with obvious pedicle primordia with both male and female genotype detected in the ovary. In conclusion, the AS cells should be defined as MSCs but with partial attributes of ESCs.
鹿茸是一种非凡的哺乳动物器官,每年可以完全再生。鹿角再生是一种基于干细胞的表型发生过程,并且鹿角干细胞(AS)可以在产后哺乳动物中启动新的鹿角生成。然而,尽管被称为干细胞,但根据干细胞标准,AS 细胞在分子水平上尚未得到表征。AS 细胞的全面表征无疑将有助于破译鹿角完全再生的机制,这是哺乳动物中唯一基于干细胞的表型发生再生的情况。在本研究中,分离了三种类型的 AS 细胞(鹿角形成性骨膜细胞 APCs,用于初始花梗和第一鹿角形成;花梗骨膜细胞 PPCs,用于年度鹿角再生;和储备间充质细胞 RMCs,用于快速鹿角生长),进行了全面的分子表征。发现一个角生长相关基因 RXFP2 仅在 AS 细胞谱系中表达,而不在面部骨膜细胞(FPCs,位于 APCs 或 PPCs 的附近)中表达,这表明 RXFP2 可能是鹿中 AS 细胞谱系的特异性标记物。我们的研究结果表明,AS 细胞表达经典 MSC 标志物,包括表面标志物 CD73、CD90、CD105 和 Stro-1。它们还表达了一些标志物,包括 Tert、Nestin、S100A4、核干细胞和 C-Myc,表明它们具有一些 ESCs 的属性。将雄性 APC 微注射到鹿胚泡中,导致一只雌性胎儿(110 天妊娠)被回收,卵巢中检测到雄性和雌性基因型的明显花梗原基。总之,AS 细胞应定义为 MSC,但具有 ESCs 的部分属性。