Shriners Hospitals for Children Portland, Portland, Oregon, United States of America.
PLoS One. 2011 Apr 11;6(4):e18795. doi: 10.1371/journal.pone.0018795.
During limb development, chondrocytes and osteoblasts emerge from condensations of limb bud mesenchyme. These cells then proliferate and differentiate in separate but adjacent compartments and function cooperatively to promote bone growth through the process of endochondral ossification. While many aspects of limb skeletal formation are understood, little is known about the mechanisms that link the development of undifferentiated limb bud mesenchyme with formation of the precartilaginous condensation and subsequent proliferative expansion of chondrocyte and osteoblast lineages. The aim of this study was to gain insight into these processes by examining the roles of c-Myc and N-Myc in morphogenesis of the limb skeleton.
METHODOLOGY/PRINCIPAL FINDINGS: To investigate c-Myc function in skeletal development, we characterized mice in which floxed c-Myc alleles were deleted in undifferentiated limb bud mesenchyme with Prx1-Cre, in chondro-osteoprogenitors with Sox9-Cre and in osteoblasts with Osx1-Cre. We show that c-Myc promotes the proliferative expansion of both chondrocytes and osteoblasts and as a consequence controls the process of endochondral growth and ossification and determines bone size. The control of proliferation by c-Myc was related to its effects on global gene transcription, as phosphorylation of the C-Terminal Domain (pCTD) of RNA Polymerase II, a marker of general transcription initiation, was tightly coupled to cell proliferation of growth plate chondrocytes where c-Myc is expressed and severely downregulated in the absence of c-Myc. Finally, we show that combined deletion of N-Myc and c-Myc in early limb bud mesenchyme gives rise to a severely hypoplastic limb skeleton that exhibits features characteristic of individual c-Myc and N-Myc mutants.
CONCLUSIONS/SIGNIFICANCE: Our results show that N-Myc and c-Myc act sequentially during limb development to coordinate the expansion of key progenitor populations responsible for forming the limb skeleton.
在肢体发育过程中,软骨细胞和成骨细胞从肢体芽间充质的凝聚中出现。这些细胞随后在单独但相邻的隔室中增殖和分化,并通过软骨内骨化过程协同作用促进骨骼生长。虽然肢体骨骼形成的许多方面都已被理解,但对于将未分化的肢体芽间充质的发育与前软骨凝聚的形成以及随后软骨细胞和成骨细胞谱系的增殖扩展联系起来的机制知之甚少。本研究的目的是通过研究 c-Myc 和 N-Myc 在肢体骨骼形态发生中的作用来深入了解这些过程。
方法/主要发现:为了研究 c-Myc 在骨骼发育中的作用,我们用 Prx1-Cre 对未分化的肢体芽间充质中的 floxed c-Myc 等位基因进行了缺失,用 Sox9-Cre 对软骨-成骨祖细胞进行了缺失,用 Osx1-Cre 对成骨细胞进行了缺失,从而对 c-Myc 进行了特征描述。我们表明 c-Myc 促进了软骨细胞和成骨细胞的增殖扩展,因此控制了软骨内生长和骨化过程,并决定了骨骼的大小。c-Myc 对增殖的控制与其对全局基因转录的影响有关,因为 RNA 聚合酶 II C 端结构域(pCTD)的磷酸化,即一般转录起始的标志物,与表达 c-Myc 的生长板软骨细胞的细胞增殖紧密相关,并且在没有 c-Myc 的情况下严重下调。最后,我们表明在早期肢体芽间充质中联合缺失 N-Myc 和 c-Myc 会导致肢体骨骼严重发育不良,表现出单个 c-Myc 和 N-Myc 突变体的特征。
结论/意义:我们的结果表明,N-Myc 和 c-Myc 在肢体发育过程中依次作用,以协调负责形成肢体骨骼的关键祖细胞群体的扩张。