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Serum deprivation induced in human lymphoblastoid Raji cells oxidative stress-associated apoptotic death and G0/G1 cell cycle arrest. Addition into culture medium of the immunomodulatory protein Seminal vesicle protein 4 (SV-IV) protected these cells against apoptosis but not against cycle arrest. The antiapoptotic activity was related to: (1) decrease of endocellular reactive Oxygen species (ROS) (2) increase of mRNAs encoding anti-oxidant enzymes (catalase, G6PD) and antiapoptotic proteins (survivin, cox-1, Hsp70, c-Fos); (3) decrease of mRNAs encoding proapoptotic proteins (c-myc, Bax, caspase-3, Apaf-1). The biochemical changes underlaying these effects were probably induced by a protein tyrosine kinase (PTK) activity triggered by the binding of SV-IV to its putative plasma membrane receptors. The ineffectiveness of SV-IV to abrogate the cycle arrest was accounted for by its downregulating effects on D1,3/E G1-cyclins and CdK2/4 gene expression, ppRb/pRb ratio, and intracellular ROS concentration. In conclusion, these experiments: (1) prove that SV-IV acts as a cell survival factor; (2) suggest the involvement of a PTK in SV-IV signaling; (3) point to cell cycle-linked enzyme inhibition as responsible for cycle arrest; (4) provide a model to dissect the cycle arrest and apoptosis induced by serum withdrawal; (5) imply a possible role of SV-IV in the survival of hemiallogenic implanting embryos.

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Cytochemical analyses was used to study the organization and content of cortical alveoli in eight species of Antarctic teleosts belonging to three different families of notothenioids: nototheniids, bathydraconids and channichthyids. Results indicated differences existed among the various species in alveolar size and distribution and in their content. In nototheniids, in particular, typical nucleoids were formed that could be large and single or small and multiple, according to the species considered. As demonstrated by the affinity to periodic acid‐Schiff (PAS) and lectin staining, these nucleoids were rich in glycoconjugates, whose nature was extremely varied in the different species, but not in lipo‐ or acidic proteins as indicated by Sudan Black B and silver salts staining. Protein extracts, electrophoresed and stained with Sudan, PAS and two lectins demonstrated that the alveoli in the two species, Trematomus bernacchii and Trematomus newnesi, contained c. 80 kDa protein rich in N‐acetylglucosamine groups. By contrast, the typical hyosophorins, described as the major alveolar content in other fishes, were apparently present only in T. newnesi

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