Reddy G V, Rodrigues V
Department of Biological Sciences, Tata Institute of Fundamental Research, Homi Bhabha Rd, Mumbai-400 005 and the National Centre for Biological Sciences, TIFR, Bangalore 560 065, India.
Development. 1999 Oct;126(20):4617-22. doi: 10.1242/dev.126.20.4617.
We have used different cell markers to trace the development of the sensory cells of the thoracic microchaete. Our results dictate a revision in the currently accepted model for cell lineage within the mechanosensory bristle. The sensory organ progenitor divides to form two secondary progenitors: PIIa and PIIb. PIIb divides first to give rise to a tertiary progenitor-PIII and a glial cell. This is followed by division of PIIa to form the shaft and socket cells as described before. PIII expresses high levels of Elav and low levels of Prospero and divides to produce neuron and sheath. Its sibling cell expresses low Elav and high Prospero and is recognized by the glial marker, Repo. This cell migrates away from the other cells of the lineage following differentiation. The proposed modification in lineage has important implications for previous studies on sibling cell fate choice and cell fate specification in sensory systems.
我们使用了不同的细胞标记物来追踪胸部微刚毛感觉细胞的发育。我们的结果表明,目前关于机械感觉刚毛内细胞谱系的公认模型需要修订。感觉器官祖细胞分裂形成两个次级祖细胞:PIIa和PIIb。PIIb首先分裂产生三级祖细胞PIII和一个神经胶质细胞。随后PIIa分裂形成如前所述的毛干和毛窝细胞。PIII高表达Elav且低表达Prospero,并分裂产生神经元和鞘细胞。它的姐妹细胞低表达Elav且高表达Prospero,并被神经胶质标记物Repo识别。该细胞在分化后从谱系中的其他细胞迁移离开。所提出的谱系修改对先前关于感觉系统中姐妹细胞命运选择和细胞命运特化的研究具有重要意义。