Literature DB >> 3537121

Natural cellular resistance of beige mice against Cryptococcus neoformans.

M R Hidore, J W Murphy.   

Abstract

Previous reports have demonstrated that natural killer (NK) cells are capable of inhibiting the growth of Cryptococcus neoformans in vitro, and recent studies indicate that adoptively transferred NK cell-enriched spleen cell populations enhance clearance of cryptococci from the tissues of cyclophosphamide-pretreated recipients. The primary objective of these studies was to confirm that NK cells participate in early clearance of C. neoformans in vivo. Secondarily, the anti-cryptococcal activities of polymorphonuclear leukocytes and macrophages were examined. Seven-week-old C57BL/6 bg/+ mice, which have normal levels of NK cell activity, were compared with their bg/bg littermates, which have impaired NK cell function. One and 3 days after injecting both groups of mice i.v. with 2 X 10(4) cryptococci, we assessed the NK cell activities in spleens, lungs, and livers and clearance of the organism from corresponding tissues as determined by the mean log10 numbers of cryptococcal colony-forming units (CFU) per organ. Three days postinfection, the mean numbers of cryptococcal CFU in lungs and spleens of bg/+ mice were significantly lower than in the corresponding organs of bg/bg mice. NK cell activities in spleens and lungs of bg/+ mice were significantly higher than were the NK cell activities in similar cell populations from bg/bg mice. In contrast, the mean numbers of cryptococcal CFU in livers of the two groups of animals were nearly equivalent, a situation not unexpected, since liver NK cell activities were extremely low and similar in both groups of animals. Although these data indicated a correlation between early clearance of cryptococci from tissues and levels of NK cell activities in the corresponding tissues, it was also possible that differences in phagocytic cell function between the bg/+ and bg/bg animals could account for the observed differences in clearance of cryptococci from the tissues. Therefore, phagocytic cells from the two groups of animals were compared with respect to their abilities to phagocytize and inhibit the growth of cryptococci and to their abilities to respond to chemotactic stimuli in vivo. Peritoneal PMNL from bg/+ and bg/bg mice were similar in their abilities to phagocytize and inhibit the growth of cryptococci, as well as in their chemotactic responses to viable cryptococci or sodium caseinate. In addition, there were no differences in splenic macrophage functions between the two groups of mice.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 3537121

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  33 in total

1.  Susceptibility of beige mutant mice to candidiasis may be linked to a defect in granulocyte production by bone marrow stem cells.

Authors:  R B Ashman; J M Papadimitriou
Journal:  Infect Immun       Date:  1991-06       Impact factor: 3.441

2.  Selection of optimal host strain for molecular pathogenesis studies on Cryptococcus gattii.

Authors:  Sudha Chaturvedi; Ping Ren; Srinivas D Narasipura; Vishnu Chaturvedi
Journal:  Mycopathologia       Date:  2005-10       Impact factor: 2.574

3.  Pathogenesis of Cryptococcus neoformans in congenitally immunodeficient beige athymic mice.

Authors:  C A Salkowski; E Balish
Journal:  Infect Immun       Date:  1990-10       Impact factor: 3.441

4.  Ras-related C3 Botulinum Toxin Substrate (Rac) and Src Family Kinases (SFK) Are Proximal and Essential for Phosphatidylinositol 3-Kinase (PI3K) Activation in Natural Killer (NK) Cell-mediated Direct Cytotoxicity against Cryptococcus neoformans.

Authors:  Richard F Xiang; Danuta Stack; Shaunna M Huston; Shu Shun Li; Henry Ogbomo; Stephen K Kyei; Christopher H Mody
Journal:  J Biol Chem       Date:  2016-02-11       Impact factor: 5.157

5.  Binding interactions of murine natural killer cells with the fungal target Cryptococcus neoformans.

Authors:  J W Murphy; M R Hidore; N Nabavi
Journal:  Infect Immun       Date:  1991-04       Impact factor: 3.441

6.  Responses of murine natural killer cells to binding of the fungal target Cryptococcus neoformans.

Authors:  M R Hidore; T W Mislan; J W Murphy
Journal:  Infect Immun       Date:  1991-04       Impact factor: 3.441

7.  Role of natural killer cells in resistance to Cryptococcus neoformans infections in mice.

Authors:  M F Lipscomb; T Alvarellos; G B Toews; R Tompkins; Z Evans; G Koo; V Kumar
Journal:  Am J Pathol       Date:  1987-08       Impact factor: 4.307

8.  Mobility of human neutrophils in response to Cryptococcus neoformans cells, culture filtrate antigen, and individual components of the antigen.

Authors:  Z M Dong; J W Murphy
Journal:  Infect Immun       Date:  1993-12       Impact factor: 3.441

9.  DAP12 Inhibits Pulmonary Immune Responses to Cryptococcus neoformans.

Authors:  Lena J Heung; Tobias M Hohl
Journal:  Infect Immun       Date:  2016-05-24       Impact factor: 3.441

10.  Direct interactions of human lymphocytes with the yeast-like organism, Cryptococcus neoformans.

Authors:  J W Murphy; M R Hidore; S C Wong
Journal:  J Clin Invest       Date:  1993-04       Impact factor: 14.808

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