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2.
Int Arch Allergy Immunol ; 160(1): 7-17, 2013.
Article in English | MEDLINE | ID: mdl-22948001

ABSTRACT

Basophils account for only 0.1-1% of all peripheral blood leukocytes. They were considered to be a redundant cell type for a long time. However, several findings show a non-redundant role for basophils in type 2 T-helper cell (Th2) immune responses in helminth infections, allergy and autoimmunity. Both immunoglobulin-E-dependent and -independent pathways have been described to contribute to basophil activation. In addition, several recent studies reported that basophils can function as antigen-presenting cells and are important in the initiation of Th2 immune responses. However, there are also conflicting studies that do not corroborate the importance of basophils in Th2 immune responses. This review discusses the role of basophils in Th2 immune responses in view of these recent findings.


Subject(s)
Antigen Presentation , Basophils/immunology , Th2 Cells/immunology , Animals , Antigen-Presenting Cells/immunology , Basophils/metabolism , Cell Differentiation , Humans , Immunoglobulin E/immunology , Inflammation/immunology , Interleukin-13/immunology , Interleukin-4/immunology , Mice
3.
Cell Transplant ; 20(8): 1271-83, 2011.
Article in English | MEDLINE | ID: mdl-21176406

ABSTRACT

Transplantation of pancreatic islets is a promising therapy for the treatment of type 1 diabetes mellitus. However, long-term islet graft survival rates are still unsatisfactory low. In this study we investigated the role of cytomegalovirus (CMV) in islet allograft failure. STZ-diabetic rats received an allogenic islet graft in combination with either an acute CMV infection or control infection. A third group received ganciclovir treatment in addition to the CMV infection. Graft function was assessed by measuring basal blood glucose levels. After sacrifice, the islet grafts were retrieved for analysis of infection and leukocyte infiltration. CMV-infected recipients demonstrated accelerated islet graft failure compared to noninfected controls. CMV infection of the graft was only observed prior to complete graft failure. Quantification of the leukocyte infiltration demonstrated increased CD8(+) T-cell and NK cell infiltration in the CMV-infected grafts compared to the controls. This suggests that CMV infection accelerates immune-mediated graft destruction. Antiviral ganciclovir treatment did not prevent accelerated graft failure, despite effectively decreasing the grade of infection. Our data confirm the recently published CITR data, which state that CMV is an independent risk factor for failure of islet grafts. Also, our data demonstrate that new approaches for preventing virus-induced islet allograft failure may be required.


Subject(s)
Cytomegalovirus Infections/virology , Cytomegalovirus/physiology , Graft Survival/immunology , Islets of Langerhans Transplantation/immunology , Animals , Antiviral Agents/pharmacology , Blood Glucose/drug effects , Blood Glucose/metabolism , Cell Movement/drug effects , Cytomegalovirus/drug effects , Cytomegalovirus Infections/immunology , Ganciclovir/pharmacology , Graft Survival/drug effects , Immunity/drug effects , Rats , Rats, Inbred Lew , Salivary Glands/drug effects , Salivary Glands/virology , Transplantation, Homologous
4.
Exp Diabetes Res ; 2008: 165360, 2008.
Article in English | MEDLINE | ID: mdl-18670618

ABSTRACT

Isolation of primary beta cells from other cells within in the pancreatic islets is of importance for many fields of islet research. However, up to now, no satisfactory method has been developed that gained high numbers of viable beta cells, without considerable alpha-cell contamination. In this study, we investigated whether rat beta cells can be isolated from nonbeta endocrine cells by manipulating the flavin adenine dinucleotide (FAD) and nicotinamide-adenine dinucleotide phosphate (NAD(P)H) autofluorescence. Beta cells were isolated from dispersed islets by flow cytometry, based on their high FAD and NAD(P)H fluorescence. To improve beta cell yield and purity, the cellular FAD and NAD(P)H contents were altered by preincubation in culture media containing varying amounts of D-glucose and amino acids. Manipulation of the cellular FAD and NAD(P)H fluorescence improves beta cell yield and purity after sorting. This method is also a fast and reliable method to measure beta cell functional viability. A conceivable application is assessing beta cell viability before transplantation.


Subject(s)
Flavin-Adenine Dinucleotide/metabolism , Insulin-Secreting Cells/cytology , Insulin-Secreting Cells/metabolism , NADP/metabolism , NAD/metabolism , Animals , Cell Culture Techniques , Cell Separation/methods , Culture Media , Flow Cytometry/methods , Glucagon-Secreting Cells/cytology , Immunohistochemistry , Islets of Langerhans/cytology , Male , Rats , Rats, Inbred Lew
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