Hinterberger T J, Cameron J A
University of Michigan, Ann Arbor.
Ontogenez. 1990 Jul-Aug;21(4):341-57.
A possibility of tissue metaplasia (transformation of one cell type into another) during limb regeneration in lower vertebrates has been a matter of vivid arguments over the last decades. These discussions are rather irreconcilable in character mainly due to the lack of reliable cell markers which permit to follow all the stages of cell transformation during metaplasia. The final conclusions can be made only if any artifacts of cell labelling are excluded. Latest findings obtained using nuclear and cytoplasmic markers are presented which suggest that many data interpreted previously as a convincing proof of metaplasia may be a consequence of the involvement of nondifferentiated cells in regeneration. Molecular biological approaches are believed to be most promising for the solution of disputable problems of tissue metaplasia. However, recent findings about actin gene hypomethylation are insufficient for any final conclusions about the possibility of metaplasia during limb regeneration. The answer to many unsolved questions of developmental biology can be made only when combined use is made of modern methods of cell and molecular biology.
在过去几十年里,低等脊椎动物肢体再生过程中组织化生(一种细胞类型转变为另一种细胞类型)的可能性一直是激烈争论的话题。这些讨论在性质上相当难以调和,主要原因是缺乏可靠的细胞标记物,无法追踪化生过程中细胞转化的所有阶段。只有排除细胞标记的任何假象,才能得出最终结论。本文介绍了使用核标记和细胞质标记获得的最新发现,这些发现表明,许多以前被解释为化生的确凿证据的数据,可能是未分化细胞参与再生的结果。分子生物学方法被认为是解决组织化生争议问题最有前景的方法。然而,最近关于肌动蛋白基因低甲基化的发现,不足以就肢体再生过程中化生的可能性得出任何最终结论。只有结合使用现代细胞和分子生物学方法,才能回答发育生物学中许多未解决的问题。