Coyle-Thompson Cathy, Oppenheimer Steven B
Center for Cancer and Developmental Biology, California State University Northridge, 18111 Nordhoff St. Northridge, CA 91330-8303, USA.
Acta Histochem. 2005;107(4):243-51. doi: 10.1016/j.acthis.2005.06.009. Epub 2005 Sep 21.
For decades most investigations into mechanisms of adhesive interactions have examined whole organisms or single cells. Results using whole organisms are often unclear because it may not be known if a probe used in an experiment is directly affecting the cellular interaction under study or if it is an indirect effect resulting from action on some other structure or pathway. Here we develop a novel approach to isolate the structural components of a cellular interaction by dissecting them out of the organism to study them in a pristine environment away from all confounding factors. We used the adhesion between the archenteron and blastocoel roof of the sea urchin gastrula stage embryo as a model that can be replicated in many other developmental and pathological systems. The isolated components of the cellular interaction and those in the whole organism possessed identical cell surface receptors and adhesive affinities.
几十年来,大多数关于黏附相互作用机制的研究都聚焦于完整生物体或单个细胞。使用完整生物体的研究结果往往不明确,因为在实验中使用的探针可能直接影响正在研究的细胞相互作用,也可能是对其他一些结构或途径产生作用而导致的间接影响,这一点并不清楚。在此,我们开发了一种新方法,通过从生物体中分离出细胞相互作用的结构成分,在远离所有混杂因素的纯净环境中对其进行研究。我们以海胆原肠胚阶段胚胎的原肠与囊胚腔顶之间的黏附作为模型,该模型可在许多其他发育和病理系统中复制。细胞相互作用的分离成分与完整生物体中的成分具有相同的细胞表面受体和黏附亲和力。