Diss. (sammanfattning) Stockholm : Karol. inst. / Härtill 6 uppsatser.

Thesis (Ph.D.) -- University of Adelaide, Department of Oral Biology, 1980.

Thesis (M.D.)--University of Hong Kong, 2001. / Includes bibliographical references (leaves 130-155) Also available in print.

Natural killer (NK) cells are a small subset of CD3-negative non-T, non-B lymphocytes that display spontaneous cytotoxic activity against a variety of normal, virus-infected, or tumor target cells without previous sensitization and with no requirement for expression of polymorphic MHC determinants on target cells. By using multicolor EPICS Elite Flow Cytometer (Coulter Corporation) and a panel of fluorochrome-conjugated Coulter Clone monoclonal antibodies (CD16-FITC, CD56-RD1, CD3-ECD and CD8-APC) , the present studies were carried out to monitor and measure the peripheral blood NK cells in seven cancer patients during chemotherapy and stem cell harvests. Flow cytometric (FCM) analysis revealed that NK cells were increased during ch'emotherapy, however as expected in many cancer or AIDS patients the immunophenotypic results did correlate poorly with the functional data obtained by 4-hour chromium-51 release cytotoxicity assay. In addition, the present studies provide direct evidence that FCM analysis can be used as a useful tool for rapid identification and purification of NK cells from cancer patients for further clinical study/application.

No description available.

Resident killer whales (Orcinus orca) in the Salish Sea use echolocation clicks to hunt for Chinook salmon, their preferred prey. An increase in underwater anthro- pogenic noise in recent decades has been identified as a threat to their survival due to auditory masking effects on these signals. Studies quantifying the effects of anthro- pogenic noise on echolocation signals have yet to be carried out due to a data gap for echolocation acoustic characteristics. In particular, to date, only one study has reported click characteristics for northern resident killer whales, and no results have been reported for southern residents. This thesis reports on acoustic recordings of resident killer whale echolocation clicks gathered over two summers in several loca- tions around Vancouver Island, and spectral and temporal characteristics extracted from them. Acoustic characteristics are reported separately for southern and north- ern resident killer whales based on 708 clicks from 19 click trains and 1277 clicks from 16 click trains, respectively. Results are further categorized into click type (slow, fast, and buzz clicks) based on inter-click interval, an indicator of foraging phase. Results show no differences in acoustic characteristics between the northern and southern killer whales, suggesting echolocation clicks do not vary between these subspecies. No significant differences are noted between slow- and fast-click characteristics, while buzz clicks appear to have some significant differences in characteristics from the oth- ers. Apparent source level values for northern and southern killer whales vary between 179-221 dB re 1 μPa at 1 m and 192-220 dB re 1 μPa at 1 m, respectively, based on the largest amplitude click from each click train (assumed to be directed towards the recording array). The values reported in this thesis will be used in subsequent noise modelling studies to quantify the effects of anthropogenic noise on resident killer whale ability to hunt for prey via echolocation signals. / Graduate

No abstract available / Dissertation (MSc)--University of Pretoria, 2008. / Zoology and Entomology / unrestricted

Cheng, Siu Fung. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2011. / Includes bibliographical references (leaves 121-141). / Abstracts in English and Chinese. / Abstract (English) --- p.ii / (Chinese) --- p.V / Acknowledgements --- p.viii / List of Abbreviations --- p.x / Table of Contents --- p.xi / Chapter Chapter 1 --- Introduction and Literature Reviews --- p.1 / Chapter 1.1 --- Bacterial Infection in Neonates --- p.1 / Chapter 1.1.1 --- Overview of Bacterial Infection in Neonates --- p.1 / Chapter 1.1.2 --- Gram-Positive Bacteria and Infection in Newborns --- p.2 / Chapter 1.1.3 --- Lipoteichoic Acid - the Immunostumulatory Component of Gram-Positive Bacteria --- p.5 / Chapter Figure 1.1 --- Schematic Representation of Gram-Positive Bacterial Cell Wall --- p.8 / Chapter Figure 1.2 --- Structure of Lipoteichoic Acid Polymer --- p.9 / Chapter 1.2 --- The Immune System of the Neonate --- p.10 / Chapter 1.2.1 --- Overview of the Human Immune System --- p.10 / Chapter 1.2.2 --- Innate Immune System --- p.10 / Chapter 1.2.3 --- Adaptive immune system --- p.13 / Chapter 1.3 --- Macrophages --- p.15 / Chapter 1.3.1 --- Overview of Macrophages --- p.15 / Chapter 1.3.2 --- Functions of Macrophages --- p.16 / Chapter 1.3.3 --- Macrophages in Gram-Positive Bacterial Infection --- p.19 / Chapter 1.4 --- Natural Killer Cells --- p.21 / Chapter 1.4.1 --- Overview of Natural Killer Cells --- p.21 / Chapter 1.4.2 --- Activation of Natural Killer Cells --- p.23 / Chapter 1.4.3 --- Functions of Natural Killer Cells --- p.24 / Chapter 1.4.4 --- Activation Markers on Natural Killer Cell Surface --- p.27 / Chapter Figure 1.3 --- Schematic Diagram of CD 107a Expression in NK Cells During Degranulation --- p.30 / Chapter 1.5 --- Interactions Between Macrophages and Natural Killer Cells --- p.31 / Chapter 1.6 --- Mitogen-Activated Protein Kinases (MAPKs) and Infection --- p.32 / Chapter 1.7 --- ApolipoproteinA-1 (ApoA-1) and Infection --- p.34 / Chapter 1.8 --- Overall Objectives of the Study --- p.36 / Chapter Chapter 2 --- Materials and Methods --- p.37 / Chapter 2.1 --- Reagents Used --- p.37 / Chapter 2.2 --- Sampling Methods --- p.41 / Chapter 2.3 --- Mononuclear Cell Isolation --- p.41 / Chapter 2.4 --- Mononuclear Cell Cryopreservation --- p.42 / Chapter 2.5 --- Induction of Macrophage from MNC culture --- p.42 / Chapter 2.6 --- Enrichment of Natural Killer (NK) Cells from MNC --- p.43 / Chapter 2.7 --- Culture of NK Cells Using Conditioned Medium Collected From LTA-Stimulated Macrophages --- p.45 / Chapter 2.8 --- Western Blotting --- p.46 / Chapter 2.9 --- Cytokines in Culture Supernatant of Macrophages --- p.50 / Chapter 2.10 --- CD107a Assay --- p.51 / Chapter 2.11 --- CD69 Assay --- p.52 / Chapter 2.12 --- Statistical Analysis --- p.53 / Chapter Figure 2.1 --- A Representative Diagram to Show NK Cell Purity After Enrichment by Immuno-Magnetic Beads --- p.55 / Chapter Figure 2.2 --- A Diagram to Illustrate the Gating Method Used in CD 107a Assay --- p.56 / Chapter Figure 2.3 --- A Diagram to Illustrate the Gating Method Used in CD69 Assay --- p.58 / Chapter Chapter 3 --- Lipoteichoic Acid - Induced Inflammatory Responses of Cord Blood Macrophages in vitro --- p.59 / Chapter 3.1 --- LTA-Stimulated Secretion of Tumor Necrosis Factor-Alpha in Cord Blood Macrophages --- p.60 / Chapter 3.2 --- LTA-Stimulated Secretion of Interleukin-6 in Cord Blood Macrophages --- p.61 / Chapter 3.3 --- LTA-Stimulated Secretion of Interleukin-12 in Cord Blood Macrophages --- p.62 / Chapter 3.4 --- LTA-Stimulated Phosphorylation of P44/42 Mitogen-Activated Protein Kinase (ERK1/2) in Cord Blood Macrophages --- p.63 / Chapter 3.5 --- The Effect of Apolipoprotein A-l Pre-Treatment on LTA-Stimulated P44/42 Mitogen-Activated Protein Kinase (Erkl/2) Phosphorylation --- p.64 / Chapter 3.6 --- Discussion --- p.65 / Chapter Figure 3.1 --- LTA-Induced TNFa Secretion by Cord Blood Macrophages --- p.73 / Chapter Figure 3.2 --- LTA-Induced IL-6 Secretion by Cord Blood Macrophages --- p.74 / Chapter Figure 3.3 --- LTA-Induced IL-12 Secretion by Cord Blood Macrophages --- p.75 / Chapter Figure 3.4 --- Phosphorylation of P44/42 MAPK (ERK1/2) Stimulated by LTA in Cord Blood Macrophages --- p.76 / Chapter Figure 3.5 --- The Effect of ApolipoproteinA-1 on LTA-Stimulated P44/42 MAPK Phosphorylation --- p.78 / Chapter Chapter 4 --- Lipoteichoic Acid - Induced Inflammatory Responses of Natural Killer Cells in vitro --- p.80 / Chapter 4.1 --- Dose-Dependent Effect of IL-15 on CD69 Expression --- p.80 / Chapter 4.2 --- Effects of LTA on CD69 Surface Expression in NK Cells --- p.82 / Chapter 4.3 --- Effects of LTA on CD 107a Surface Expression in NK Cells --- p.84 / Chapter 4.4 --- Discussion --- p.87 / Chapter Figure 4.1 --- Dose-Dependent Effect of IL-15 on Cord Blood NK Cells CD69 Surface Expression --- p.93 / Chapter Figure 4.2 --- Effects of LTA and IL-15 on CD69 surface Expression in NK Cells --- p.95 / Chapter Figure 4.3 --- Effects of LTA and IL-15 on CD 107a surface Expression in NK Cells --- p.97 / Chapter Chapter 5 --- Effects of LTA-Primed Macrophage-Conditioned Medium on Autologous Natural Killer Cell Activation --- p.99 / Chapter 5.1 --- Effects of Macrophage-Conditioned Medium on Autologous NK Cell CD 107a Expression --- p.100 / Chapter 5.2 --- Effects of LTA-Stimulated Macrophages on Autologous NK cells CD69 Expression --- p.102 / Chapter 5.3 --- Discussion --- p.105 / Chapter Figure 5.1 --- Flow Chart of the Experiment Design --- p.110 / Chapter Figure 5.2 --- Effects of Macrophage-Conditioned Medium on Autologous NK CD 107a Expression --- p.111 / Chapter Figure 5.3 --- Effects of Macrophage-Conditioned Medium on Autologous NK CD69 Expression --- p.113 / Chapter Chapter 6 --- Conclusion and General Discussion --- p.115 / Chapter 6.1 --- Conclusion --- p.115 / Chapter 6.2 --- Potential Applications of the Findings --- p.117 / Chapter 6.3 --- Limitations --- p.118 / Chapter 6.4 --- Further Studies --- p.119 / References --- p.121

Thesis (M.S.)--University of British Columbia, 1996. / Includes bibliographical references (p. 51-61). Also available in electronic format via Internet.

Sightings and acoustic recordings from 1984 to 1989 of northern resident killer whales (Orcinus orca) from Johnstone Strait off north eastern Vancouver Island and from King Island on the central British Columbia coast were analysed to examine the hypothesis that northern resident whales move seasonally in their range to areas where salmon are available. Killer whales were most abundant in Johnstone Strait between July and October and infrequent during the remainder of the year. The increase in whale abundance during summer coincided with the migration of salmon (Oncorhynchus spp.) from offshore into Johnstone Strait. The occurrence near King Island in spring 1989 of the same resident whales that are seen in Johnstone Strait during summer, coincided with runs of sockeye and chinook salmon. During July, August and September of 1984 through 1988, killer whale sightings were recorded virtually daily in the Johnstone Strait. Observations of killer whales in Johnstone Strait during the summer of 1988 showed that whales foraged along shore and in areas of strong current where salmon occur in high densities. Of the 16 killer whale pods in the northern resident community, however, less than half were present more than 15% of summer days (1984 to 1988). Regression results between numbers of whale days per week from each pod and numbers of salmon per week showed that the occurrence pods that were present on more than 15% of summer days in Johnstone Strait was positively and significantly associated with the abundance of sockeye and pink salmon (six pods). In addition to these, the occurrence of one pod that spent less than 15% of summer days in the Strait was positively and significantly associated with chum salmon. Together these results support the hypothesis that northern resident killer whales select their habitat seasonally to feed on available salmon. The results also lead to the hypothesis that within the northern resident community each pod has a seasonal home ranges. / Land and Food Systems, Faculty of / Graduate