Search

We use simultaneous measurements from the Wind and ACE spacecraft to determine the spatial properties of both interplanetary (IP) shocks and the shock-associated energetic particle events. We combine plasma, magnetic field and energetic particle data from ACE and Wind for 124 energetic storm particle (ESP) events from 1998 to 2003 and examine the spatial and temporal variations of these events in the Earth's vicinity. We find that even though the two spacecraft were occasionally separated by more than 400 RE, the plasma, field, and energetic particle time-intensity profiles during the events were very similar. In addition, we find that the ion composition and energy spectra in individual IP shock events are identical at the two spacecraft locations. We also use the fitted shock velocity along the normal from ACE and estimate the shock transit time to Wind location. In general, there is poor agreement between the estimated transit time and the actual measured transit time. Hence, our assumptions that a) the IP shock at 1 AU propagates radially, and/or b) the IP shock is spherically symmetric at 1 AU are not valid. In this paper, we will also study, for the first time, the anisotropy measurements of low-energy IP shock-associated ions at both ACE and Wind. We will then compare these new anisotropy analyses with locally measured shock parameters and identify possible signatures of different shock acceleration processes as predicted by the first-order Fermi and shock-drift models.

Cardiac myocytes maintained in cell culture develop hypertrophy both in response to mechanical loading as well as to receptor-mediated signaling mechanisms. However, it has been shown that the hypertrophic response to these stimuli may be modulated through effects of intercellular contact achieved by maintaining cells at different plating densities. In this study, we show that the myocyte plating density affects not only the hypertrophic response and features of the differentiated phenotype of isolated adult myocytes, but also plays a significant role influencing myocyte survival in vitro. The native rod-shaped phenotype of freshly isolated adult myocytes persists in an environment which minimizes myocyte attachment and spreading on the substratum. However, these conditions are not optimal for long-term maintenance of cultured adult cardiac myocytes. Conditions which promote myocyte attachment and spreading on the substratum, on the other hand, also promote the re-establishment of new intercellular contacts between myocytes. These contacts appear to play a significant role in the development of spontaneous activity, which enhances the redevelopment of highly differentiated contractile, junctional, and sarcoplasmic reticulum structures in the cultured adult cardiomyocyte. Although it has previously been shown that adult cardiac myocytes are typically quiescent in culture, the addition of beta-adrenergic agonists stimulates beating and myocyte hypertrophy, and thereby serves to increase the level of intercellular contact as well. However, in densely-plated cultures with intrinsically high levels of intercellular contact, spontaneous contractile activity develops without the addition of beta-adrenergic agonists. In this study, we compare the function, morphology, and natural history of adult feline cardiomyocytes which have been maintained in cultures with different levels of intercellular contact, with and without the addition of beta-adrenergic agonists. Intercellular contact, communication, and transmission of contractile forces between myocytes appears to play a primary role in remodeling the 2-dimensional cell layer into a parallel alignment of elongated myocytes with highly developed intercalated disk-like junctions. This highly differentiated state is very stable, and cultures which achieve this state exhibit significantly greater longevity than more sparsely plated myocytes. These myocytes typically continue beating, and survive from 6 to more than 12 weeks in culture. When this level of contact and differentiation are not achieved, even among beta-adrenergic stimulated myocytes, contractile activity is not sustained, myofibrils atrophy, there is little or no development of junctional complexes, and the period of myocyte viability is typically no more than 5 weeks in vitro.

Fluctuations in hemodynamic load have been documented to modulate contractile protein turnover and myofibrillar structure in the heart; however, the relative importance of active and passive loading in regulating adult cardiocyte growth remains unresolved. To address this issue at the cellular level, adult feline cardiocytes were cultured either on Silastic membranes or plastic surfaces. Cardiocyte-laden membranes were stretched 10% of their rest length to enhance passive loading, whereas heart cells cultured on plastic or Silastic were field stimulated at 1 Hz to mimic active loading. Turnover of contractile proteins and structural integrity of the contractile-cytoskeletal apparatus were monitored for periods ranging from 4 to 72 h. Active and passive loading elevated contractile protein synthesis nearly equally (approximately 50%) and promoted the attachment of remodeled myofibrils to vinculin-positive focal contacts and/or costameres during the first 24 h of loading. Thereafter, rates of contractile protein synthesis returned to control values in passively stretched heart cells but remained elevated in field-stimulated cultures. The fractional rate of growth was increased significantly (approximately 8%/day) in electrically paced cells, whereas in passively stretched cardiocytes the growth rate rose only modestly (approximately 2%/day). Changes in the rate of myocyte growth appeared more closely correlated with the development of focal contacts and myofibril remodeling than with changes in myofibrillar protein turnover per se. 2,3-Butanedione monoxime, nifedipine, and, to a lesser extent, ryanodine blocked field-stimulated contractile protein synthesis and myofibrillar remodeling but had no impact on protein turnover or myofibril reassembly in passively loaded cardiocytes. The results of these experiments imply that both active and passive loading stimulate contractile protein turnover and myofibril remodeling, but the generation of active tension accelerates cardiocyte growth to a greater extent than passive loading. Furthermore, pharmacological interventions suggest that unique pathways may mediate these cellular events in actively and passively loaded adult cardiocytes.

Cultured adult rabbit cardiac myocytes treated with recombinant growth factors display enhanced rates of protein accumulation (ie, growth) in response to insulin and insulin-like growth factors (IGFs), but epidermal growth factor, acidic or basic fibroblast growth factor, and platelet-derived growth factor failed to increase contractile protein synthesis or growth of the heart cells. Insulin and IGF-1 increased growth rates by stimulating anabolic while simultaneously inhibiting catabolic pathways, whereas IGF-2 elevated growth modestly by apparently inhibiting lysosomal proteolysis. Neutralizing antibodies directed against either IGF-1 or IGF-2 or IGF binding protein 3 blocked protein accumulation. A monoclonal antibody directed against the IGF-1 receptor also inhibited changes in protein turnover provoked by recombinant human IGF-1 but not IGF-2. Of the other growth factors tested, only transforming growth factor-beta 1 increased the fractional rate of myosin heavy chain (MHC) synthesis, with beta-MHC synthesis being elevated and alpha-MHC synthesis being suppressed. However, the other growth factors were able to modestly stimulate the rate of DNA synthesis in this preparation. Bromodeoxyuridine labeling revealed that these growth factors increased DNA synthesis in myocytes and nonmyocytes alike, but the heart cells displayed neither karyokinesis or cytokinesis. In contrast, cocultures of cardiac myocytes and nonmyocytes and nonmyocyte-conditioned culture medium failed to enhance the rate of cardiac MHC synthesis or its accumulation, implying that quiescent heart cells do not respond to "conditioning" by cardiac nonmyocytes. These findings demonstrated that insulin and the IGFs promote passively loaded cultured adult rabbit heart cells to hypertrophy but suggest that other growth factors tested may be limited in this regard.

Escape of neutral hydrogen (H) and nitrogen (N) from Triton's maintains a large neutral cloud, called the Triton torus, in Neptune's magnetosphere. We have developed the first detailed Monte Carlo simulation model of the Triton torus that includes the collisionality, the complex geometry, the injection of two neutral species from Triton (H and N), and the combined effects of photoionization, electron impact ionization, and charge exchange. Ionization in Neptune's plasma sheet was modeled using Voyager plasma observations. Collisions cause both the H and N neutral clouds to become more radially extended, both toward Neptune and out beyond the magnetopause, as well as more extended in latitude, when compared with collisionless models. Moreover, collisions of H with the much more massive N greatly enhance the collisional ejection of H from the system and into Neptune's atmosphere. This effect decreases the probability of H ionization within the magnetosphere relative to that for N, and furthermore causes model results for two-species injection from Triton to differ significantly from those for H injection alone. For a hydrogen escape rate from Triton of 5 x 10(exp 25)/s, as given by photo-chemical models of Triton's upper atmosphere, a nitrogen escape rate of 5 x 10(exp 24)/s gives proton and N(+) sources of 5.6 x 10(exp 24)/s and 3.3 x 10(exp 24)/s, respectively, whose ratio is close to the observed ratio of protons to heavies. A nitrogen escape rate of 2 x 10(exp 25)/s, yields an N(+) source more than twice that of protons, inconsistent with the Voyager data.