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by neuroguy
4883 days ago
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From the FAQ -
Why not begin with simple organisms like C.elegans? There are two problems here. The first is feasibility; the second is the relevance of our results.
Feasibility. Neuroscientists have mapped all of C.elegans’ 300 or so neurons. However, enormous amounts of key data needed are still missing. For instance we do not have enough data on the physiology and pharmacology of C. Elegans neurons and synapses. And we still have limited data on the distribution of ion channels, receptors and other proteins on neurons, synapses and glia. Without this data we cannot build unifying models. A second problem is how easy it is to obtain the data. The crucial requirement for unifying models is the ability to access the data needed. Obtaining a deep understanding of the molecular machinery of a single neuron or a single synapse is just as difficult in C. Elegans as in human beings. And many datasets – particularly data on cognition - are actually easier to acquire in rodents, or even in humans. So we can’t just say: “let’s do this quickly in worms and do complex brains later”: we have to solve the same basic challenges, whatever brain we model. What we are actually doing is building a generic strategy we can use to reconstruct any brain. Relevance: Studying the “simple” nervous systems of organisms like C.elegans or drosophila, is obviously very important, particularly for molecular and genetic studies. However the organization, electrophysiology and function of the mammalian brain are quite different. One of the HBP’s most important goals is to contribute to the development of new treatments for brain disease. But pharmaceutical companies already have great difficulties in translating results from mouse to human beings; with simpler organisms these problems become much worse. If we want to make a real contribution to clinical research, it is probably unwise to invest heavily in simple systems, so distant from the human brain. |
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