Effects of prolonged mitosis on neural stem cells in vivo during development
Microcephaly patients are born with a brain size >3 standard deviations below normal and have mild to severe cognitive deficits. 12 microcephaly-linked genes identified in human genetics studies encode microtubule/centrosome-associated proteins and mutations in these genes are strongly tied to disrupted mitotic processes in neural stem cells during cortical development. Yet, how perturbed neural stem cell mitosis kinetics affects cell fate following neural stem cell division is not well understood. Our lab recently discovered prolonging mitosis of mouse neural progenitors, either ex vivo or in vitro, alters fate decisions forcing early increased neurogenic divisions at the expense of maintaining the stem cell pool. Yet, the consequences of prolonged mitosis in vivo, and directly in human stem cells, remain unexplored. Additionally, how prolonged mitosis mechanistically affects cell stress response and cell fate decisions during development is not well-studied.
Through in vivo pharmacological approaches, and in vitro culture of human neural progenitors, I provide evidence that prolonged mitosis in vivo directly alters cell fate, and that this consequence of prolonged mitosis is conserved from mice to humans. I find prolonged mitosis of neural stem cells in vivo results in increased phosphorylation of H2AX in mitosis, and increased pATR in a subset of newborn cells. P53 is then activated in a subset of daughter cells and upregulates downstream target genes. Within approximately the first cell cycle, prolonged mitosis results in an increase in neurogenic fates in the daughter cell population at the expense of progenitor renewal. Conditional loss of P53 rescues these effects on cell fate, while loss of BAX does not. Additionally, I find that time to cell death occurs on a log-normal distribution within the population. These experiments suggest that identifying the factors sensitive to prolonged prometaphase/mitosis arrest that transduce P53 activating signals is critical for our understanding of microcephaly etiologies. Together, data presented in this thesis suggest prolonged mitosis directly alters cell fate in vivo during cortical development and in human neural stem cells, that response to prolonged mitosis is relatively specific, involving P53 signaling, and that prolonged mitosis is a main contributing factor to microcephaly as a result of mitotic gene disruption.
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.
Rights for Collection: Duke Dissertations
Works are deposited here by their authors, and represent their research and opinions, not that of Duke University. Some materials and descriptions may include offensive content. More info