Price J S, Oyajobi B O, Russell R G
Department of Human Metabolism and Clinical Biochemistry, Sheffield University Medical School, UK.
Eur J Clin Nutr. 1994 Feb;48 Suppl 1:S131-49.
The field of bone cell biology is clearly of relevance to the problem of stunting in children, as in the final analysis the cells of the growing long bone are the ultimate 'regulators'. It is the alterations in the functions of these cells that manifests as a reduction in height. Normal longitudinal growth is achieved by the coordinated recruitment, proliferation, differentiation, maturation and eventual death of the cells of growth plate and bone. Cellular activity is closely regulated by endocrine factors acting directly or indirectly, with factors produced locally and stored within the bone and cartilage microenvironment having a critical role in intercellular communication. Disruption of any of these processes can lead to growth disturbances, since it only requires a defect in a single gene to have profound effects. Studies in recent years have shed light on the biochemical and molecular effects of cytokines and growth factors and have shown that these regulatory molecules may mediate the effects of certain hormones important in controlling growth. However, the complex interrelationship of these molecules is still not clear. Notwithstanding, understanding of the mechanisms involved in bone remodelling is increasing, as this area attracts much research because of the high incidence of metabolic bone disease in Western society. Although studies of adult bone remodelling are of relevance, there is a requirement for increased research directed specifically at the mechanisms of endochondral ossification and its regulation. Longitudinal bone growth is a challenge to the cell biologist, since it is an accelerated cycle of cellular division and differentiation, within which it is not easy to separate events temporally and spatially. In addition, different regulatory mechanisms are probably important at different stages of growth. Another difficulty impeding progress in this field is the lack of appropriate animal models for research. Much information has come from studies involving rodents, and species differences must always be taken into account. Larger mammals such as the growing piglet or the calf are probably more appropriate for the study of postnatal longitudinal growth in man. If the mechanisms of stunting are to be established at a cellular level, a number of approaches need to be considered. Studies need to be designed using more appropriate animal models, and conditions such as nutritional intake, immunological challenges, chronic intestinal diseases and mechanical loading need to be manipulated. Any effects on longitudinal growth may then be studied temporally and correlated with non-invasive measurements including assays of hormones, cytokines, growth factors and proteins known to regulate their activity.(ABSTRACT TRUNCATED AT 400 WORDS)
骨细胞生物学领域显然与儿童发育迟缓问题相关,因为归根结底,正在生长的长骨细胞是最终的“调节者”。正是这些细胞功能的改变表现为身高降低。正常的纵向生长是通过生长板和骨骼细胞的协同募集、增殖、分化、成熟以及最终死亡来实现的。细胞活动受到直接或间接作用的内分泌因子的密切调节,骨骼和软骨微环境中产生并储存的局部因子在细胞间通讯中起关键作用。这些过程中任何一个的破坏都可能导致生长紊乱,因为只需一个基因缺陷就能产生深远影响。近年来的研究揭示了细胞因子和生长因子的生化及分子效应,并表明这些调节分子可能介导某些对控制生长很重要的激素的作用。然而,这些分子之间复杂的相互关系仍不清楚。尽管如此,由于西方社会代谢性骨病的高发病率,这个领域吸引了大量研究,人们对骨重塑所涉及机制的理解也在不断增加。虽然对成人骨重塑的研究有相关性,但需要增加专门针对软骨内成骨机制及其调节的研究。纵向骨生长对细胞生物学家来说是一项挑战,因为它是细胞分裂和分化的加速循环,在这个循环中,很难在时间和空间上区分各个事件。此外,不同的调节机制可能在生长的不同阶段很重要。阻碍该领域进展的另一个困难是缺乏合适的研究动物模型。很多信息来自涉及啮齿动物的研究,必须始终考虑物种差异。较大的哺乳动物,如正在生长的仔猪或小牛,可能更适合研究人类出生后的纵向生长情况。如果要在细胞水平上确定发育迟缓的机制,需要考虑多种方法。研究需要使用更合适的动物模型进行设计,并且需要控制营养摄入、免疫挑战、慢性肠道疾病和机械负荷等条件。然后可以在时间上研究对纵向生长的任何影响,并将其与包括激素、细胞因子、生长因子和已知调节其活性的蛋白质检测在内的非侵入性测量结果相关联。(摘要截选至400字)