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Heuser, J.

Publications and source records attributed to Heuser, J..

2 recordsLinked to original sources

The structural basis of long-term potentiation in hippocampal synapses, revealed by EM-imaging of lanthanum-induced synaptic vesicle recycling

Hippocampal neurons in tissue-culture were exposed to the trivalent cation lanthanum for short periods (15 to 30 minutes) and prepared for electron microscopy (EM), to evaluate the stimulatory effects of this cation on synaptic ultrastructure. Not only were characteristic ultrastructural changes of exaggerated synaptic vesicle turnover seen within the presynapses of these cultures - - including synaptic vesicle depletion and proliferation of vesicle-recycling structures - - but the overall architecture of a large proportion of the synapses in the cultures was dramatically altered, due to large postsynaptic bulges or herniations into the presynapses. Moreover, in most cases these postsynaptic herniations or protrusions produced by lanthanum were seen by EM to distort or break or perforate the so-called postsynaptic densities (PSDs) that harbor receptors and recognition-molecules essential for synaptic function. These dramatic EM-observations lead us to postulate that such PSD-breakages or perforations could very possibly create essential substrates or tags for synaptic growth, simply by creating fragmented free-edges around the PSDs, into which new receptors and recognition-molecules could be recruited more easily, and thus they could represent the physical substrate for the important synaptic-growth process known as "long-term potentiation" (LTP). All of this was created simply in hippocampal tissue-cultures, and simply by pushing synaptic vesicle recycling way beyond its normal limits with the trivalent cation lanthanum; but we argue in this report that such fundamental changes in synaptic architecture - - given that they can occur at all - - could also occur at the extremes of normal neuronal activity, which are presumed to lead to learning and memory.

neuroscience↗

Contacting domains that segregate lipid from solute transporters in malaria parasites

While membrane contact sites (MCS) between intracellular organelles are abundant1, and cell-cell junctions are classically defined2, very little is known about the contacts between membranes that delimit extracellular junctions within cells, such as those of chloroplasts and intracellular parasites. The malaria parasite replicates within a unique organelle, the parasitophorous vacuole (PV) but the mechanism(s) are obscure by which the limiting membrane of the PV, the parasitophorous vacuolar membrane (PVM), collaborates with the parasite plasma membrane (PPM) to support the transport of proteins, lipids, nutrients, and metabolites between the cytoplasm of the parasite and the cytoplasm of the host erythrocyte (RBC). Here, we demonstrate the existence of multiple micrometer-sized regions of especially close apposition between the PVM and the PPM. To determine if these contact sites are involved in any sort of transport, we localized the PVM nutrient-permeable and protein export channel EXP2, as well as the PPM lipid transporter PfNCR1. We found that EXP2 is excluded from, but PfNCR1 is included within these regions of close apposition. Thus, these two different transport systems handling hydrophilic and hydrophobic substances, respectively, assume complementary and exclusive distributions. This new structural and molecular data assigns a functional significance to a macroscopic membrane domain.

microbiology↗