Hippocampal Neuron

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In the paper by Goslin and Banker (1989) observations about the modifiable state of axons is presented. While the paper makes useful observations about the hippocampal neurites, the experimentation clearly needed to go further to answer many unanswered questions about neuronal polarity. The study revealed that the closer a cut is made to the soma, the more likely the axon would be to regrow somewhere else. However, this study was mainly observational and there were many questions about neuronal polarity and why the length of the neurite would have an effect on the formation of the axon. Based on observations like these, Toriyama et al. (2010) attempts address the mechanisms of how neurons can sense neurite length in order to identify the longest …show more content…

(2010) did a study to define the role of the centrosome in microtubule nucleation and found that the centrosome loses its function as a microtubule organizing center in hippocampal neurons and axons extend independently of centrosomal microtubule nucleation. This led to the conclusion that the decentralization of microtubule nucleation and the dismantling of the centrosome may be essential in the enabling axon branching. Jacobson et al. (2006) did a study to see where kinesins translocate in developing neurons. This study came to the conclusion that the view that all neurons are morphologically and molecularly identical and a break in symmetry is an indication of axon formation is incorrect. The results suggested that at that stage, growth and molecular differentiation are separate events. After reading this paper along with the controversial study of Calderon de Anda et al. (2005) many questions have arisen about whether the instruction for polarized cell growth is truly determined before the neurons are formed. While Steiss et al. (2010) explores the role of the centrosome during neuronal polarization and the necessity of its positioning during, further studies could still explore the possibility of neuritic fate being predetermined. Future studies can also investigate why Calderon de Anda et al. (2005) saw a phenotype with two long neurites instead of several short neurites when neurons had two centrosomal clusters. Could there have also be other factors being affected during the process of generating neurons with more than one centrosome? Cytochalasin D, which was used to block cytokinesis is an inhibitor of actin polymerization. The role of centrosomes in action polymerization should be further explored to better understand the role centrosomes may play a role in actin nucleation and how that relates to neuritic growth and phenotype. It is clear that the phenotype they saw was due to defects in neuronal polarity and it would be interesting to

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