Provisional mapping of the gene for a cell surface marker, GA-1, in the red-necked wallaby Macropus rufogriseus

A series of M. rufogriseus-mouse somatic cell hybrids was constructed and analysed cytologically, enzymatically and immunologically. A monoclonal antibody, GA-1, was prepared against an M. rufogriseus cell surface antigen on an M. rufogriseus-mouse somatic cell hybrid. A gene determining the expression of this antigen was provisionally assigned to the long arm of the M. rufogriseus chromosome 3. The monoclonal antibody also reacted with an M. rufus (red kangaroo)-mouse somatic cell hybrid containing only the M. rufus chromosome 5, the G-banded chromosome identical to M. rufogriseus 3q. The results also suggest synteny of the genes for the marsupial enzymes hypoxanthine phosphoribosyltransferase and phosphoglycerate kinase-A.     

Efficacy of Translators for Establishing Mercury Total Maximum Daily Loads

In Oregon's Willamette River, methylmercury levels in fish triggered health advisories and the need for a mercury Total Maximum Daily Load (TMDL). A translator was used to relate surface water total mercury (C_THg) to dissolved methylmercury concentrations (C_DMeHg). The USEPA's Spreadsheet-based Ecological Risk Assessment for the Fate of Mercury (SERAFM) was used to elucidate the annual relationship between mercury loads, C_THg, and C_DMeHg, to investigate whether C_THg is a reasonable predictor for C_DMeHg, and to consider how load reductions may be affected by the differing annual trajectories of total and methylmercury concentrations. Modeling and observations suggest that C_THg and C_DMeHg are not directly proportional, that C_THg is an inconsistent predictor of C_DMeHg, that a single point estimate translator could easily misjudge their relationship, and that C_DMeHg may be more responsive to environmental factors than to load alone. While a translator is convenient for relating C_THg and C_DMeHg for regulatory purposes, it may not, due to environmental factors unrelated to loading, be the most efficacious means for this purpose. TMDLs relying on a translator are advised to conduct co-located total and methylmercury sampling with sufficient frequency to provide information on the watershed-specific annual relationship between total mercury and methylmercury.     

Intervesicular exchange of lipids with weak acid and weak base characteristics: influence of transmembrane pH gradients

Transmembrane pH gradients have previously been shown to induce an asymmetric transmembrane distribution of simple lipids that exhibit weak acid or basic characteristics (Hope, M.J. and Cullis, P.R. (1987) J. Biol. Chem. 262, 4360-4366). In the present study we have examined the influence of proton gradients on the inter-vesicular exchange of stearylamine and oleic acid. We show that vesicles containing stearylamine immediately aggregate with vesicles containing phosphatidylserine and that disaggregation occurs subsequently as stearylamine equilibrates between the two vesicle populations. Despite visible flocculation during the aggregation phase, vesicle integrity is maintained. Stearylamine is the only lipid to exchange, fusion does not occur and vesicles are able to maintain a proton gradient. When stearylamine is sequestered to the inner monolayer in response to a transmembrane pH gradient (inside acidic) aggregation is not observed and diffusion of stearylamine to acceptor vesicles is greatly reduced. The ability of delta pH-dependent lipid asymmetry to modulate lipid exchange is also demonstrated for fatty acids. Oleic acid can be induced to transfer from one population of vesicles to another by maintaining a basic interior pH in the acceptor vesicles. Moreover, it is shown that the same acceptor vesicles are capable of depleting serum albumin of bound fatty acid. These results are discussed with respect to the mechanism and modulation of lipid flow between membranes both in vitro and in vivo.     

Adult human dermal fibroblasts exposed to nanosecond electrical pulses exhibit genetic biomarkers of mechanical stress

BackgroundExposure of cells to very short (<1 µs) electric pulses in the megavolt/meter range have been shown to cause a multitude of effects, both physical and molecular in nature. Physically, nanosecond electrical pulses (nsEP) can cause disruption of the plasma membrane, cellular swelling, shrinking and blebbing. Molecularly, nsEP have been shown to activate signaling pathways, produce oxidative stress, stimulate hormone secretion and induce both apoptotic and necrotic death. We hypothesize that studying the genetic response of primary human dermal fibroblasts exposed to nsEP, will gain insight into the molecular mechanism(s) either activated directly by nsEP, or indirectly through electrophysiology interactions.MethodsMicroarray analysis in conjunction with quantitative real time polymerase chain reaction (qRT-PCR) was used to screen and validate genes selectively upregulated in response to nsEP exposure.ResultsExpression profiles of 486 genes were found to be significantly changed by nsEP exposure. 50% of the top 20 responding genes coded for proteins located in two distinct cellular locations, the plasma membrane and the nucleus. Further analysis of five of the top 20 upregulated genes indicated that the HDFa cells’ response to nsEP exposure included many elements of a mechanical stress response.ConclusionsWe found that several genes, some of which are mechanosensitive, were selectively upregulated due to nsEP exposure. This genetic response appears to be a primary response to the stimuli and not a secondary response to cellular swelling.General significanceThis work provides strong evidence that cells exposed to nsEP interpret the insult as a mechanical stress.     

The Meaning of Time

Abstract

Jeremy Rifkin. Time Wars. New York: Touchstone Books, Simon & Schuster, 1989. 302 pp. $9.95 paperback.