A new role for PGRP-S (Tag7) in immune defense: lymphocyte migration is induced by a chemoattractant complex of Tag7 with Mts1

PGRP-S (Tag7) is an innate immunity protein involved in the antimicrobial defense systems, both in insects and in mammals. We have previously shown that Tag7 specifically interacts with several proteins, including Hsp70 and the calcium binding protein S100A4 (Mts1), providing a number of novel cellular functions. Here we show that Tag7–Mts1 complex causes chemotactic migration of lymphocytes, with NK cells being a preferred target. Cells of either innate immunity (neutrophils and monocytes) or acquired immunity (CD4⁺ and CD8⁺ lymphocytes) can produce this complex, which confirms the close connection between components of the 2 branches of immune response.     

Changes in the electrical activity of the hippocampus during elaboration of an inhibitory reaction in the dog

A conditioned alimentary instrumental reflex was elaborated in three dogs with chronically implanted electrodes to a consecutive complex conditioned stimulus consisting of two equal acoustic stimuli separated by a pause. At first, the animals reacted with motor reactions during the whole action of the complex signal. Then inhibition of reaction was elaborated at first in pause and then in response to the preparatory stimulus. In the process of stabilization of inhibition, there was an increase of similarity of spectral composition of hippocampal theta-rhythm with the values obtained in the inter-signal period. Conclusion is made that the hippocampus is not a structure necessary for the elaboration of internal inhibition. The frequency of hippocampal theta-rhythm may serve as a characteristic of the property called in Pavlov's school mobility of the nervous system.     

Changes in TNF and IL-6 production after diphtheria toxoid vaccination: drug modulation of the cytokine levels

The effect of vaccination with diphtheria toxoid (AD-M) on TNF and IL-6 production has been studied in humans. In the present study it was demonstrated that immunization with AD-M resulted in changes of in vitro TNF and IL-6 production by peripheral blood mononuclear cells. TNF release was suppressed but IL-6 production was stimulated. On the other hand, serum levels of TNF were markedly increased over a period of 3 weeks. It was also demonstrated that the postvaccinal cytokine production disturbances may be corrected by pretreatment with a new synthetic hexapeptid (Imunofan((R))). It is possible that the imunofan treatment could prevent some postvaccinal complications.     

Plasminogen activator and collagenase production by cultured capillary endothelial cells

Cultured bovine capillary endothelial (BCE) cells produce low levels of collagenolytic activity and significant amounts of the serine protease plasminogen activator (PA). When grown in the presence of nanomolar quantities of the tumor promoter 12-O-tetradecanoyl phorbol-13-acetate (TPA), BCE cells produced 5-15 times more collagenolytic activity and 2-10 times more PA than untreated cells. The enhanced production of these enzymes was dependent on the dose of TPA used, with maximal response at 10(-7) to 10(-8) M. Phorbol didecanoate (PDD), an analog of TPA which is an active tumor promoter, also increased protease production. 4-O-methyl-TPA and 4α-PDD, two analogs of TPA which are inactive as tumor promoters, had no effect on protease production. Increased PA and collagenase activities were detected within 7.5 and 19 h, respectively, after the addition of TPA. The TPA-stimulated BCE cells synthesized a urokinase-type PA and a typical vertebrate collagenase. BCE cells were compared with bovine aortic endothelial (BAE) cells and bovine embryonic skin (BES) fibroblasts with respect to their production of protease in response to TPA. Under normal growth conditions, low levels of collagenolyic activity were detected in the culture fluids from BCE, BAE, and BES cells. BCE cells produced 5-13 times the basal levels of collagenolytic activity in response to TPA, whereas BAE cells and BES fibroblasts showed a minimal response to TPA. Both BCE and BAE cells exhibited relatively high basal levels of PA, the production of which was stimulated approximately threefold by the addition of TPA. The observation that BCE cells and not BAE cells produced high levels of both PA and collagenase activities in response to TPA demonstrates a significant difference between these two types of endothelial cells and suggests that the enhanced detectable activities are a property unique to bovine capillary and microvessel and endothelial cells.     

Separation of dissociated thyroid follicular and parfollicular cells: association of serotonin binding protein with parafollicular cells

Parafollicular cells (PC) of the sheep thyroid gland are neural crest derivatives that synthesize and release the biogenic amine serotonin (5-HT) as well as the hormone calcitonin. The thyroid also contains a highly specific serotonin-binding protein (SBP). Separation of dissociated thyroid cells was done to study the cellular localization of SBP and to develop a means of isolating PC for study. Various methods were used to obtain an enriched and purified population of PC. Minced thyroid glands were enzymatically dissociated and the cells were layered on a Ficoll linear density gradient. Fractions obtained from the gradient were examined for cell number, viability, 5-HT concentration, SBP activity, and morphology by electron microscopy. One of the fractions was found to be enriched in PC. High levels of 5-HT and SBP were also found in this fraction, whereas these levels were low where the majority of cells were found. This PC-rich fraction, however, contained numerous follicular cells (FC); therefore, additional approaches to cell separation were used. FC can be stimulated in vitro with thyroid stimulating hormone (TSH) to become intensely phagocytic. When stimulated cells were incubated in the presence of silica microspheres, the FC engulfed the microspheres, which were toxic to them. PC did not become phagocytic and were unharmed by the microspheres. Suspended cells, after incubation with microspheres, were centrifuged on a discontinuous gradient, and a PC-rich fraction was obtained. Silica, however, interfered with analysis of SBP. Another method to take advantage of the phagocytic potential of FC was therefore used. TSH-stimulated cell suspensions were passed through a column of sepharose to which thyroglobulin had been coupled. Stimulated FC apparently adhered to the beads and were retained by the columns. Fractions eluting from the columns were greatly enriched with PC. These fractions contained high levels of 5-HT and SBP, and considerably reduced FC contamination was found by quantitative electron microscopy. It is concluded that SBP is localized to PC in the sheep thyroid. The idea that these cells resemble serotonergic neurons in their mechanisms of 5-HT storage is supported.     

Structure of arctic fox (Alopex lagopus beringensis) colonies in the northern extremity of Bering Island

Data on the spatial structure of an Arctic fox (Alopex lagopus beringensis) colony were obtained in July-August 1995, using walk counts and observations near living dens around the Northern rookery of the northern fur seals located on Bering Island (Commander Islands). The home ranges of 31 Arctic fox families (61 adults and 145 pups inhabiting 66 dens) were found over 27 km of the coastline. Sixty individuals (3 adults and 57 pups) were marked by color ear-tags. Among adult foxes, 24 (39.3%) were recognized as females and 12 (19.7%) as males; the sex of 25 (41.0%) foxes was not recognized. Among 57 marked cubs, 26 (45.6%) were females and 31 (54.4%) were males. The best studied families (13) had 3–11 pups (6.7 ± 0.7, on average). The survival of cubs at an age younger than 2.0–2.5 months was 82.5%; 30.8% of the families consisted of more than two adults. The distribution of the Arctic fox dens and home ranges along the coastline has been studied; specific features of the location of dens have been described. In the studied area, Arctic foxes have been foraging on birds (67.6% of dens with food remains), northern fur seals (40.5), other marine mammals (13.5), Pacific salmon (29.7), and reindeer (2.7%), as well as on amphipods and voles. Rich constant food sources (rookeries, marine bird colonies, and spawning places of the blueback salmon) were found in 7 home ranges of the Arctic fox; 6 home ranges included temporary food sources (spawning streams of the humpback salmon); and 18 home ranges were poor in food resources. Arctic foxes whose home ranges lie within 6–7 km around a “food patch” used the concentrated food resources together. Food resources are supposed to become important only after the raised pups turn to self-feeding. Differences in the use of space, foraging and breeding of the two Arctic fox subspecies (A. l. beringensis and A. l. semenovi), and arrangement of colonies around the northern fur seal rookeries are discussed.     

Palatability and feeding preferences of Uresiphita maorialis (Lepidoptera: Crambidae) for three Sophora species

In a three-hour bioassay, we tested the palatability and feeding preferences of Uresiphita maorialis (kōwhai moth) for Sophora tetraptera, Sophora microphylla and Sophora prostrata. Palatability tests showed no differences among the Sophora species. Feeding preferences, on the other hand, showed that S. tetraptera and S. microphylla leaves are preferred over S. prostrata leaves. Our results support our field observations in Wellington city parks and gardens showing that S. tetraptera and S. microphylla plants frequently have higher densities of larvae than S. prostrata.