Boyan B D, Sylvia V L, Dean D D, Schwartz Z
Department of Orthopaedics, University of Texas Health Science Center, San Antonio 78284-7774, USA.
Connect Tissue Res. 1996;35(1-4):63-70. doi: 10.3109/03008209609029175.
Interpretation of the cell biology literature, as it relates to formation and mineralization of calcifying tissues, is complicated by the plethora of models available. Some culture models use heterogeneous populations of cells while others use relatively homogeneous populations. The issues are further confused by comparison of monolayer and three dimensional cultures. In addition, transformed and nontransformed cell lines are also used. As little clinical data about the age and sex of the original donor for many of these cell lines is lacking, it is impossible to know where in the cell lineage the cells were when they were isolated, yet this information can have a direct impact on the data obtained and their interpretation. Furthermore, many responses are attributed to the cell, while much of the effect observed may be targeted to the matrix. These issues are discussed and a potential mechanism explaining how cells can modulate events in the matrix nongenomically is presented.
由于存在大量可用模型,与钙化组织的形成和矿化相关的细胞生物学文献的解读变得复杂。一些培养模型使用异质细胞群体,而另一些则使用相对同质的细胞群体。单层培养和三维培养的比较进一步混淆了这些问题。此外,还使用了转化细胞系和未转化细胞系。由于许多这些细胞系缺乏关于原始供体年龄和性别的临床数据,因此无法知道细胞在分离时处于细胞谱系的哪个位置,但这些信息可能会对获得的数据及其解读产生直接影响。此外,许多反应归因于细胞,而观察到的许多效应可能针对的是基质。本文讨论了这些问题,并提出了一种潜在机制,解释细胞如何通过非基因组方式调节基质中的事件。