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1.
J Reprod Immunol ; 117: 81-8, 2016 09.
Article in English | MEDLINE | ID: mdl-27529307

ABSTRACT

INTRODUCTION: Lymphangiogenesis is the formation of new vessels from pre-existing lymphatic vessels. Data on lymphangiogenesis in the placenta of HIV-infected pre-eclamptics are sparse and the findings are conflicting. The aim of this novel study was to evaluate LYVE-1 immunoexpression in the placenta of HIV infected normotensive versus pre-eclamptic women. METHODS: Placental tissue was obtained from normotensive and pre-eclamptic women stratified according to their HIV status. The pre-eclamptic group was divided into early (<34 weeks) and late (>34 weeks) onset. Immunohistochemistry utilized mouse anti-human LYVE-1 antibody and was morphometrically evaluated. RESULTS: LYVE-1 immunostaining was localized within endothelium of the arterial supply and venous drainage of both conducting and exchange villi as well as within medial cells of arteries. LYVE-1 immunostained macrophage-like cells were observed within the fetal and maternal circulation. LYVE-1 immunoexpression was higher (p=0.0001) in HIV positive cohort, regardless of pregnancy and villous type. Irrespective of HIV status and pregnancy type, LYVE-1 immunoexpression was significantly elevated in the conducting compared to the exchange villi (p=0.01). LYVE-1 immunoexpression was higher in N and LOPE compared to EOPE groups for both conducting and exchange villi types respectively (p=0.0001 and p=0.006). There is a decrease of LYVE-1 expression in EOPE+ (conducting villi) and EOPE- (exchange villi) compared to N and LOPE subgroups. CONCLUSION: This study provides a novel insight into an up-regulation of LYVE-1 expression in the fetal circulation of conducting and exchange villi of HIV-infected pre-eclamptics.


Subject(s)
Endothelium, Vascular/metabolism , HIV Infections/immunology , HIV/immunology , Lymphatic Vessels/pathology , Placenta/pathology , Pre-Eclampsia/immunology , Vesicular Transport Proteins/metabolism , Adolescent , Adult , Endothelium, Vascular/pathology , Female , Gestational Age , HIV Infections/complications , Humans , Immunochemistry , Lymphangiogenesis , Male , Placental Circulation , Pregnancy , Vesicular Transport Proteins/immunology , Young Adult
2.
Ann Bot ; 92(3): 401-8, 2003 Sep.
Article in English | MEDLINE | ID: mdl-12881405

ABSTRACT

Although fungi cause a recognized problem during storage of recalcitrant seeds of many tropical species, there are no data to date on defence strategies of these seeds against fungal attack. To ascertain whether recalcitrant seeds of Avicennia marina elaborate compounds that might suppress fungal proliferation during hydrated storage, the production and efficacy of beta-1,3-glucanase (EC 3.2.1.39) and chitinase (EC 3.2.1.14) were studied in relation to histopathological changes. Freshly harvested seeds had low beta-1,3-glucanase and chitinase activities and fluorescence microscopy revealed progressive deterioration of the internal tissues of these seeds associated with fungal infection during hydrated storage. In seeds treated to minimize associated fungi (clean seeds), beta-1,3-glucanase and chitinase activities increased significantly during 10 d of hydrated storage. Similar high levels of activity were observed when these seeds were experimentally infected with Fusarium moniliforme and subjected to further storage. The histopathological observations indicated delayed disease development in the 10-d clean-storage period, although the hypersensitive response was not observed. The results suggest that, although the recalcitrant seeds of A. marina elaborate some antifungal enzymes, there is a lack of effective defence strategies that might lead to successful responses against fungal infections.


Subject(s)
Avicennia/microbiology , Fusarium/physiology , Plant Diseases/microbiology , Seeds/microbiology , Avicennia/chemistry , Chitinases/metabolism , Glucan 1,3-beta-Glucosidase , Microscopy, Fluorescence , Plant Proteins/isolation & purification , beta-Glucosidase/metabolism
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