A mitogen gradient of dorsal midline Wnts organizes growth in the CNS
SG Megason, AP McMahon - 2002 - journals.biologists.com
2002•journals.biologists.com
Cell cycle progression and exit must be precisely patterned during development to generate
tissues of the correct size, shape and symmetry. Here we present evidence that dorsal-
ventral growth of the developing spinal cord is regulated by a Wnt mitogen gradient. Wnt
signaling through the β-catenin/TCF pathway positively regulates cell cycle progression and
negatively regulates cell cycle exit of spinal neural precursors in part through transcriptional
regulation of cyclin D1 and cyclin D2. Wnts expressed at the dorsal midline of the spinal …
tissues of the correct size, shape and symmetry. Here we present evidence that dorsal-
ventral growth of the developing spinal cord is regulated by a Wnt mitogen gradient. Wnt
signaling through the β-catenin/TCF pathway positively regulates cell cycle progression and
negatively regulates cell cycle exit of spinal neural precursors in part through transcriptional
regulation of cyclin D1 and cyclin D2. Wnts expressed at the dorsal midline of the spinal …
Cell cycle progression and exit must be precisely patterned during development to generate tissues of the correct size, shape and symmetry. Here we present evidence that dorsal-ventral growth of the developing spinal cord is regulated by a Wnt mitogen gradient. Wnt signaling through the β-catenin/TCF pathway positively regulates cell cycle progression and negatively regulates cell cycle exit of spinal neural precursors in part through transcriptional regulation of cyclin D1 and cyclin D2. Wnts expressed at the dorsal midline of the spinal cord, Wnt1 and Wnt3a, have mitogenic activity while more broadly expressed Wnts do not. We present several lines of evidence suggesting that dorsal midline Wnts form a dorsal to ventral concentration gradient. A growth gradient that correlates with the predicted gradient of mitogenic Wnts emerges as the neural tube grows with the proliferation rate highest dorsally and the differentiation rate highest ventrally. These data are rationalized in a ‘mitogen gradient model’ that explains how proliferation and differentiation can be patterned across a growing field of cells. Computer modeling demonstrates this model is a robust and self-regulating mechanism for patterning cell cycle regulation in a growing tissue.
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