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Biotech / Medical : Cortex (Cor) [formerly CORX] -- Ignore unavailable to you. Want to Upgrade?

To: mammoth who wrote (589)	10/19/1998 5:53:00 PM
From: Mike McFarland	Respond to of 1255

hehe, yup, now that risk is only -100% a good time to load up! One of the biotech fellas supplied me with part of an article on one of the other threads, enjoy. J Comp Neurol 1998 Jul 20;397(1):139-47 Amyloid beta protein is internalized selectively by hippocampal field CA1 and causes neurons to accumulate amyloidogenic carboxyterminal fragments of the amyloid precursor protein. Bahr BA, Hoffman KB, Yang AJ, Hess US, Glabe CG, Lynch G Cortex Pharmaceuticals, Inc., Irvine, California 92618, USA. bahr@uconnvm.uconn.edu A critical issue concerning Alzheimer's disease is its selectivity, which leads to cellular degeneration in certain brain areas but not in others, and whether this pathogenic selectivity involves products of the amyloid precursor protein APP). Here, we show that the amyloid beta protein Abeta1-42 is accumulated gradually and is retained intact by field CA1, but not by other subdivisions, of organotypic hippocampal slice cultures. In contrast, the slightly shorter Abeta1-40 peptide was not sequestered selectively. Sequestration of Abeta1-42 was followed by the build-up of carboxyterminal fragments of the endogenous precursor protein that were identified by immunoprecipitation. Unlike the peptide uptake, this induction appeared to be stochastic at the cellular level. In addition, the APP fragments were distributed more broadly within the CA1 pyramidal neurons than the sequestered Abeta1-42, and they appeared to be localized to synaptic terminals in the molecular layer of the dentate gyrus and in the stratum lacunosum-moleculare of the subfield CA3. Concentrations of synaptophysin, a presynaptic marker, decreased as the number of neurons producing amyloidogenic species increased. These results indicate that exogenous Abeta1-42 sets into motion a sequence that involves 1) selective uptake of the peptide by vulnerable cells at risk in Alzheimer's disease, 2) markedly enhanced production of amyloidogenic precursor material, and 3) slow deterioration of central synapses. Sorry, I'm not qualified to decode all that, but it's fun to run through the index of a text book and do some reading. That's all I do lately--my biotech stocks get me interested in the science, and whether they're good investments or not I end up learning something. Lame way to invest, but fun for hobby. -MM