APOPTOTIC CELL-DEATH IN THE LIMB AND ITS RELATIONSHIP TO PATTERN-FORMATION

Citation
Zf. Zakeri et Hs. Ahuja, APOPTOTIC CELL-DEATH IN THE LIMB AND ITS RELATIONSHIP TO PATTERN-FORMATION, Biochemistry and cell biology, 72(11-12), 1994, pp. 603-613
Citations number
60
Categorie Soggetti
Biology
ISSN journal
08298211
Volume
72
Issue
11-12
Year of publication
1994
Pages
603 - 613
Database
ISI
SICI code
0829-8211(1994)72:11-12<603:ACITLA>2.0.ZU;2-O
Abstract
Detection of cell death throughout embryogenesis demonstrates its impo rtance in the normal form and function of the organism. We have examin ed cellular death during normal limb development by use of markers tha t display the morphology of cell death, the presence of phagocytic cel ls, and lysosomal activity. In addition in situ labeling confirms frag mentation of DNA in the mammalian limb. By these criteria, cell death in the developing limb can be categorized as type 1 or apoptotic cell death. However, the signal(s) responsible for cellular destruction and activation of phagocytosis by neighboring cells or recruited macropha ges remain to be identified. The decision for cellular fate during dev elopment and regulation of it once the decision is made are key questi ons. To address the specific question of what determines that one cell will die while its neighbor survives, we have used compounds, such as retinoic acid (RA), that have been shown to alter the pattern of norm al development. We and others have shown that RA does indeed alter the pattern of cell death to the extent of inducing malformations in the limb. The mouse mutant Hammertoe (Hm) provides an abnormal system in w hich the pattern of cell death is specifically altered in the interdig ital regions of the limb. Our preliminary data suggest that RA can als o introduce cell death between digits 2, 3, 4, and 5 of the Hm mutant where there was no cell death to begin with. Our observations of the e ffect of RA on mutant limbs suggest that a direct relationship between RA and cell death does exist and that this interaction may be require d for correct pattern formation. The alteration in the pattern of cell death in the mutant mouse is of great interest, since it would provid e a rare example of specific correction of a birth defect by direct in tercession against the physiological effect of the mutation.