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L Segel

Publications and source records attributed to L Segel.

14 recordsLinked to original sources
PubMed2000

Autoreceptors, membrane potential and the regulation of transmitter release.

It has been suggested that depolarization per se can control neurotransmitter release, in addition to its role in promoting Ca2+ influx. The 'Ca2+ hypothesis' has provided an essential framework for understanding how Ca2+ entry and accumulation in nerve terminals controls transmitter release. Yet, increases in intracellular Ca2+ levels alone cannot account for the initiation and termination of release; some additional mechanism is needed. Several experiments from various laboratories indicate that membrane potential has a decisive role in controlling this release. For example, depolarization causes release when Ca2+ entry is blocked and intracellular Ca2+ levels are held at an elevated level. The key molecules that link membrane potential with release control have not yet been identified: likely candidates are presynaptic autoreceptors and perhaps the Ca2+ channel itself.

Animals↗
PubMed1998

The diffusion of molecules in axonal plasma membranes: the sites of insertion of new membrane molecules and their distribution along the axon surface.

The neuronal cell surface consists of two domains, the somatodendritic and axonal plasma membranes. Each domain serves different functions, and has a different complement of membrane molecules. Since membrane molecules are able to diffuse in the plane of the plasma membrane lipid bilayer, with diffusion coefficients ranging from 10-8 cm 2 s-1 for lipids to 10-10 cm 2 s-1 for proteins, mechanisms must exist to prevent as intermixing of membrane molecules from each domain by diffusion. Presented here is a theoretical analysis of the distribution of axonal molecules in both growing and non-growing axons based on two models for the insertion of these molecules into the axonal membrane, namely insertion exclusively at the distal end of the axon, or insertion with equal probability all along the axon. In all cases, assuming that the molecules have a finite half-life in the axonal membrane, compositional differences between the axonal and somatodendritic membranes can be obtained that are similar to those observed in other polarized cells, even in the absence of a physical barrier to prevent the intermixing of membrane molecules. Moreover, our analyses demonstrate that the diffusion of membrane molecules in the plane of the axonal lipid bilayer is a sufficiently slow process to preclude the possibility that membrane molecules are inserted into axonal membranes at a site remote from their final location, and then move to their final locations for diffusion. Thus, in long axons, for membrane molecules that are localized all along the length of the axon, mechanisms must exist for their insertion in the axonal membrane at sites all along the axon, and not just at the distal end.

Animals↗
PubMed1998

MHC-linked syngeneic developmental preference in thymic lobes colonized with bone marrow cells: a mathematical model.

Reconstitution of the T-cell compartment after bone marrow transplantation depends on successful colonization of the thymus by bone-marrow-derived progenitor cells. Recent studies compared the development of syngeneic and allogeneic bone-marrow-derived cells in co-cultures with lymphoid-depleted fetal thymus explants, leading to the discovery of MHC-linked syngeneic developmental preference (SDP) in the thymus. To determine the nature of cell interactions among the bone marrow and thymic elements that might underlie SDP, we analyzed this phenomenon by mathematical modeling. The results indicate that syngeneic mature T cells, responsible for inducing this preference, probably interfere both with the seeding of allogeneic bone-marrow-derived thymocyte progenitors in the thymic stroma and with their subsequent proliferation. In addition, the possibility of augmented death among the developing allogeneic thymocytes cannot be ruled out.

Bone Marrow Transplantation↗
PubMed1997

"First step" negative feedback accounts for inhibition of fast neurotransmitter release.

This paper is concerned with feedback inhibition of neurotransmitter release by the neurotransmitter itself. We put forward the idea that, similar to multistep biochemical processes, feedback inhibition acts on the initial step in the chain of events that lead to release. Using experimental results carried out on glutamatergic synapses in crayfish, we show that the "first step" hypothesis can account for all experimental results. Our modeling suggests that the biochemical implementation of this inhibition involves the formation of a second messenger, whose production is triggered by binding of transmitter to the autoreceptor. We argue that the autoreceptor is a key part of the release-inducing machinery.

Animals↗
PubMed1997

A mechanism for discharge of charged excitatory neurotransmitter.

Excitatory neurotransmitter is charged, so that emptying of a transmitter-containing vesicle (discharge) would seem to require considerable energy. Even if the energy problem is surmounted and discharge thereby made possible, there is still a problem of making the discharge fast enough (considerably less than 1 ms). Proposed here is a mechanism wherein discharge of charged transmitter is accompanied by the influx of cocharged ions or coefflux of counter-charged particles (ion interchange). It is shown theoretically that ion interchange obviates the necessity for a separate energy source and can provide the observed rapid vesicle discharge.

Acetylcholine↗
PubMed1995

Lymphocyte development in irradiated thymuses: dynamics of colonization by progenitor cells and regeneration of resident cells.

Lymphocyte development in irradiated thymuses was analyzed using two complementary strategies: an in vitro experimental model and computer simulations. In the in vitro model, fetal thymus lobes were irradiated and the regeneration of cells that survived irradiation were examined, with the results compared to those of reconstitution of the thymus by donor bone marrow cells and their competition with the thymic resident cells. In vitro measurements of resident cell kinetics showed that cell proliferation is slowed down significantly after a relatively low (10 Gy) irradiation dose. Although the number of thymocytes that survived irradiation remained low for several days post-irradiation, further colonization by donor cells was not possible, unless performed within 6 h after irradiation. These experimental results, coupled with the analysis by computer simulations, suggest that bone marrow cell engraftment in the irradiated thymus may be limited by the presence of radiation-surviving thymic resident cells and the reduced availability of seeding niches.

Animals↗
PubMed1995

Modulated excitability: a new way to obtain bursting neurons.

Classical burster models are based on a fast system that either oscillates or is quiescent, depending on temporarily fixed values of slow variables. In a study of the lobster heart ganglion, we found a new type of burster for which the fast system is globally stable for all relevant fixed values of the slow variables. We describe how this burster works and speculate on its biological significance.

Animals↗
PubMed1994

Colonization of the thymus by T cell progenitors: models for cell-cell interactions.

The early events of T-cell generation, i.e. seeding of bone marrow-derived progenitor cells onto the thymic stroma, involve a small fraction (up to 1%) of thymus cells and are not presently observable. However, these events are crucial in determining the outcome of thymic colonization. In previous studies we utilized an experimental in vitro model of thymic reconstitution by bone marrow cells to compare normal thymocyte development with the development in conditions of T-cell deficiency, and, in particular, in aging. These studies showed that progenitor cells from old donor bone marrow are deficient in their ability to colonize the thymus, in spite of their ability to divide earlier upon seeding. In this study we apply mathematical and computer modelling in order to analyse early T-cell development and the causes for the developmental disadvantage of old donor bone marrow cells. The results indicate that the competition for seeding niches in the thymic stroma determines the outcome of colonization.

Aging↗
PubMed1994

Diffusion cannot govern the discharge of neurotransmitter in fast synapses.

In the present work we show that diffusion cannot provide the observed fast discharge of neurotransmitter from a synaptic vesicle during neurotransmitter release, mainly because it is not sufficiently rapid nor is it sufficiently temperature-dependent. Modeling the discharge from the vesicle into the cleft as a continuous point source, we have determined that discharge should occur in 50-75 microseconds, to provide the observed high concentrations of transmitter at the critical zone.

Animals↗
PubMed1993

A new method for expressing axonal size: rat optic nerve analysis.

Analysis of the shape of the cross sections of adult rat optic nerve axons reveals that the majority of axons do not have a true circular shape. Therefore, determination of axonal size has to utilize methods of approximation. The method presented here utilizes three calculated parameters for expression of axonal size: (i) axonal diameter, as calculated from its area, or (ii) axonal diameter, as calculated from its perimeter, both assuming axonal shape to be a perfect circle and (iii) axonal shape factor, which represents the divergence of the axon from a perfect circular shape. The use of the calculated axonal diameter, with a correction for its shape factor, provides a normalized way of expressing axonal size.

Animals↗
PubMed1990

Release kinetics as a tool to describe drug effects on neurotransmitter release.

A procedure is developed wherein the time course of neurotransmitter release is used to discern the mechanism of effects of drugs on the release process. It is shown, in agreement with experiments, that the time course of release is insensitive to the temporal distribution of intracellular Ca2+ concentration. The time course is also invariant to the steps in the release process that are Ca2+ dependent. The most influential events in determining the time course of release are shown to be the steps associated with the slowest forward rate constant and all the backward steps. The procedure was examined for its ability to explain the effects on release of the poison curare and those of temperature. It appears that curare probably blocks release by lowering the rate constant associated with the rate limiting step in release. Increasing temperature is predicted to increase both the forward and the backward rate constants, but not to the same extent.

Animals↗
PubMed1986

A new method for determining co-operativity in neurotransmitter release.

It has been accepted for some time that neurotransmitter release exhibits a co-operative dependence on calcium. Here we suggest a new procedure for estimating the co-operativity, based on the early rise of synaptic delay histograms of induced release at low quantal content. Measurements of such histograms at the lobster neuromuscular junction are reported. On the basis of this data, and also of data from the literature for other species, a re-examination is made of the conventional hypothesis that the kinetics of release is primarily determined by the time course of entry and removal of calcium ions. Two major new hypotheses for the nature of co-operativity are discussed, both containing the additional feature that membrane depolarization activates a molecule or complex that only then can bind calcium and induce release. The measurements confirm the hypothesis that the co-operativity arises from the action of several complexes between calcium and a depolarization-activated molecule to initiate the release of a vesicle. The co-operativity exponent is estimated to be between three and five in lobster neuromuscular junction and also in crayfish, macrobrachium, and frog.

Allosteric Regulation↗