Integrating levels of bone growth control: From stem cells to body proportions.

Q1 Biochemistry, Genetics and Molecular Biology
Brett J Kagan, Alberto Rosello-Diez
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引用次数: 2

Abstract

The study of the mechanisms controlling organ size during development and regeneration is critical to understanding how complex life arises from cooperating single cells. Long bones are powerful models in this regard, as their size depends on a scaffold made from another tissue (cartilage, composed of chondrocytes), and both tissues interact during the growth period. Investigating long bone growth offers a valuable window into the processes that integrate internal and external cues to yield finely controlled size of organs. Within the cellular and molecular pathways that control bone growth, the regulation of stem-cell renewal, along with amplification and differentiation of their progeny, are key to understanding normal and perturbed long-bone development. The phenomenon of "catch-up" growth-where cellular hyperproliferation occurs following injury to restore a normal growth trajectory-reveals key aspects of this regulation, such as the fact that bone growth is target-seeking. The control mechanisms that lead to this behavior are either bottom-up or top-down, and the interaction between these modes is likely critical to achieve a highly nuanced, yet flexible, degree of control. The role of cartilage-intrinsic mechanisms has been well studied, establishing a very solid groundwork for this field. However, addressing the unanswered questions of bone growth arguably requires new hypotheses and approaches. Future research could for example address to what extent extrinsic signals and cells, as well as communication with other tissues, modulate intra-limb and inter-organ growth coordination. This article is categorized under: Adult Stem Cells, Tissue Renewal, and Regeneration > Tissue Stem Cells and Niches Establishment of Spatial and Temporal Patterns > Regulation of Size, Proportion, and Timing Vertebrate Organogenesis > Musculoskeletal and Vascular.

骨生长控制的整合水平:从干细胞到身体比例。
研究发育和再生过程中控制器官大小的机制对于理解复杂生命是如何从合作的单细胞中产生的至关重要。在这方面,长骨是强有力的模型,因为它们的大小取决于由另一种组织(软骨,由软骨细胞组成)制成的支架,两种组织在生长期间相互作用。研究长骨生长提供了一个有价值的窗口,了解整合内部和外部线索以产生精细控制的器官大小的过程。在控制骨生长的细胞和分子途径中,干细胞更新的调节及其后代的扩增和分化是理解正常和受干扰的长骨发育的关键。“追赶”生长现象——细胞在损伤后发生过度增殖以恢复正常生长轨迹——揭示了这种调节的关键方面,例如骨骼生长是寻找目标的事实。导致这种行为的控制机制要么是自底向上的,要么是自顶向下的,这些模式之间的交互可能是实现高度微妙但灵活的控制程度的关键。软骨内在机制的作用已经得到了很好的研究,为这一领域奠定了非常坚实的基础。然而,解决骨生长的悬而未决的问题可能需要新的假设和方法。例如,未来的研究可以解决外在信号和细胞,以及与其他组织的交流,在多大程度上调节肢体内和器官间的生长协调。本文分类如下:成体干细胞、组织更新和再生>组织干细胞和生态位建立的时空模式>脊椎动物器官发生的大小、比例和时间调节>肌肉骨骼和血管。
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期刊介绍: Developmental biology is concerned with the fundamental question of how a single cell, the fertilized egg, ultimately produces a complex, fully patterned adult organism. This problem is studied on many different biological levels, from the molecular to the organismal. Developed in association with the Society for Developmental Biology, WIREs Developmental Biology will provide a unique interdisciplinary forum dedicated to fostering excellence in research and education and communicating key advances in this important field. The collaborative and integrative ethos of the WIREs model will facilitate connections to related disciplines such as genetics, systems biology, bioengineering, and psychology. The topical coverage of WIREs Developmental Biology includes: Establishment of Spatial and Temporal Patterns; Gene Expression and Transcriptional Hierarchies; Signaling Pathways; Early Embryonic Development; Invertebrate Organogenesis; Vertebrate Organogenesis; Nervous System Development; Birth Defects; Adult Stem Cells, Tissue Renewal and Regeneration; Cell Types and Issues Specific to Plants; Comparative Development and Evolution; and Technologies.
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