T lymphocyte subsets in patients with malignant melanoma

Summary T lymphocyte subset profiles were determined by monoclonal antibodies on cryopreserved peripheral blood lymphocytes from 57 patients with malignant melanoma and 19 healthy controls. Quantitation of percentages of total T cells (OKT3.PAN), helper (OKT4.IND) or suppressor (OKT8.SUP) cells, and the ratio of helper/suppressor subsets revealed no correlation of these markers with stage of disease or clinical outcome. A sequential study of these markers on peripheral blood lymphocytes from three stage I melanoma patients with subsequent recurrent disease showed no fluctuations that could be correlated to tumor progression. This study indicates that there is no systemic imbalance in T cell subsets in malignant melanoma and that quantitation of these subsets cannot predict the clinical course of this disease.     

Mass spectrometry investigation of glycosylation on the NXS/T sites in recombinant glycoproteins

We used a targeted proteomics approach to investigate whether introduction of new N-linked glycosylation sites in a chimeric protein influence the glycosylation of the existing glycosylation sites. To accomplish our goals, we over-expressed and purified a chimeric construct that contained the Fc region of the IgG fused to the exons 7 & 8 of mouse ZP3 (IgG-Fc-ZP3E7 protein). Immunoglobulin heavy chain (IgG-HC protein) was used as control. We then analyzed the IgG-HC and IgG-Fc-ZP3E7 proteins by liquid chromatography-tandem mass spectrometry (LC–MS/MS) and by Western blotting (WB). We concluded that in control experiments, the glycosylation site was occupied as expected. However, in the IgG-Fc-ZP3E7 protein, we concluded that only one out of three NXS/T glycosylation sites is occupied by N-linked oligosaccharides. We also concluded that in the IgG-Fc-ZP3E7 protein, upon introduction of additional potential NXS/T glycosylation sites within its sequence, the original NST/S glycosylation site from the Fc region of the IgG-Fc-ZP3E7 protein is no longer glycosylated. The biomedical significance of our findings is discussed.     

Susceptibility of California gastropods to an introduced South African sabellid polychaete, Terebrasabella heterouncinata

Abstract. The outer surfaces of the shells of living marine gastropods are often colonized by other organisms. However, only one species, the sabellid worm Terebrasabella heterouncinata , is able to settle in the aperture of living gastropods. Native to South Africa, and introduced to California, this worm is a pest of abalone aquaculture and has been a threat to native gastropods in California. We investigated the intrinsic susceptibility of 15 marine gastropods from California to this apertural fouling organism. Intrinsic susceptibility was significantly different among gastropod species. Overall, caenogastropods tended to be more resistant than were the vetigastropods and patellogastropods. This suggests that variability in susceptibility could be due to characteristics associated with closely related gastropod hosts. However, this only partially explained the variation in susceptibility to individuals of T. heterouncinata . Intrinsic susceptibility was not associated with potential host species from similar habitats. We discuss host susceptibility to T. heterouncinata , including implications for potential control of this pest species, and for understanding factors enabling this polychaete to inhabit the apertural region, an area typically free of all other epibionts.     

Quelques apports à la théorie de l’Évolution,de la « Synthèse orthodoxe » à la « Super synthèse évo-dévo » 1970–2009 : un point de vue

Some contributions to evolutionary theory, from the “orthodox” Synthesis to the “Evo-devo Super synthesis” 1970–2009: A point of view. The “Modern Synthesis” of evolutionary biology coalesced and revitalized evolutionary theory beginning in the 1930s. It stressed the explanatory power of natural selection and gradual change to account for the processes that govern natural populations today, as well as patterns in the history of life. In the past 40 years, the synthesis has been challenged on various fronts ranging from paleontology to developmental biology, systematics, biogeography, and molecular and developmental biology. Several of its central propositions have been modified and expanded as a result. How well the synthesis continues to be effective will depend on its continued ability to test its central propositions and the efficacy of its central mechanisms, particularly on the basis of new evidence from emerging fields of study.