Autotransplantation of hepatic granulomas into the skin of mice with Schistosoma mansoni infection
Journal Article
·
· J. Invest. Dermatol.; (United States)
Hepatic egg granulomas of mice infected with Schistosoma mansoni were transplanted into the skin of the same animal and changes occurring to macrophages, eosinophils, and mast cells over time were studied by light and electron microscopy and by autoradiographic techniques. Disappearance of cellular components about the egg granulomas occurred within 1 week; the entire implant became encapsulated by inflammatory cells and stroma. By 3 weeks mononuclear cells and macrophages reorganized the granulomas around the eggs and neutrophils disappeared. Activated macrophages contained both secretory rough endoplasmic reticulum and lysosomal-dense bodies. Granuloma size increased up to 5 weeks after implantation and mast cells and eosinophils tended to migrate into the granulomas. The mast cell index always remained lower than in the original hepatic granulomas, while eosinophils were seen in large numbers. During 3 to 8 weeks after implantation mononuclear cells undergoing DNA synthesis in the granulomas ranged from 2.9-4.8%. Some 3-week-old autotransplants were injected with /sup 3/H-thymidine and biopsied from 1 to 21 days later. Labeled mononuclear cells peaked in the granulomas by 10 days (24%) and the numbers fell off sharply after that. These findings indicate that autologously implanted schistosome egg granulomas can be maintained successfully in the skin for prolonged periods with marked ingress of macrophages and eosinophils. The autoradiographic data suggest the lesions are high turnover granulomas.
- Research Organization:
- Department of Dermatology, University of California, San Francisco, USA
- OSTI ID:
- 6578693
- Journal Information:
- J. Invest. Dermatol.; (United States), Journal Name: J. Invest. Dermatol.; (United States) Vol. 79:3; ISSN JIDEA
- Country of Publication:
- United States
- Language:
- English
Similar Records
Course of Schistosoma mansoni infection in thymectomized rats. [Gamma radiation]
Cutaneous sensitivity induced by immunization with irradiated Schistosoma mansoni cercariae. I. Induction, elicitation, and adoptive transfer analysis of cell-mediated cutaneous sensitivity
Murine eosinophils labeled with indium-111 oxine: localization to delayed hypersensitivity reactions against a schistosomal antigen and to lymphokine in vivo
Journal Article
·
Thu Jul 01 00:00:00 EDT 1976
· J. Immunol.; (United States)
·
OSTI ID:7187425
Cutaneous sensitivity induced by immunization with irradiated Schistosoma mansoni cercariae. I. Induction, elicitation, and adoptive transfer analysis of cell-mediated cutaneous sensitivity
Journal Article
·
Sun Jun 01 00:00:00 EDT 1986
· Cell. Immunol.; (United States)
·
OSTI ID:5003471
Murine eosinophils labeled with indium-111 oxine: localization to delayed hypersensitivity reactions against a schistosomal antigen and to lymphokine in vivo
Journal Article
·
Thu Mar 31 23:00:00 EST 1983
· Blood; (United States)
·
OSTI ID:5776788
Related Subjects
550301 -- Cytology-- Tracer Techniques
550901 -- Pathology-- Tracer Techniques
551001* -- Physiological Systems-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ANIMAL CELLS
ANIMALS
AUTORADIOGRAPHY
BIOLOGICAL MATERIALS
BLOOD
BLOOD CELLS
BODY
BODY FLUIDS
CONNECTIVE TISSUE CELLS
DIGESTIVE SYSTEM
DISEASES
DYNAMIC FUNCTION STUDIES
EOSINOPHILS
GLANDS
GRANULOMAS
HELMINTHS
IMMUNE REACTIONS
ISOTOPE APPLICATIONS
LABELLED COMPOUNDS
LEUKOCYTES
LIVER
MACROPHAGES
MAMMALS
MAST CELLS
MATERIALS
MICE
NEOPLASMS
ORGANS
PHAGOCYTES
PLATYHELMINTHS
RODENTS
SCHISTOSOMA
SKIN
SOMATIC CELLS
TRANSPLANTS
TREMATODES
TRITIUM COMPOUNDS
VERTEBRATES
550901 -- Pathology-- Tracer Techniques
551001* -- Physiological Systems-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ANIMAL CELLS
ANIMALS
AUTORADIOGRAPHY
BIOLOGICAL MATERIALS
BLOOD
BLOOD CELLS
BODY
BODY FLUIDS
CONNECTIVE TISSUE CELLS
DIGESTIVE SYSTEM
DISEASES
DYNAMIC FUNCTION STUDIES
EOSINOPHILS
GLANDS
GRANULOMAS
HELMINTHS
IMMUNE REACTIONS
ISOTOPE APPLICATIONS
LABELLED COMPOUNDS
LEUKOCYTES
LIVER
MACROPHAGES
MAMMALS
MAST CELLS
MATERIALS
MICE
NEOPLASMS
ORGANS
PHAGOCYTES
PLATYHELMINTHS
RODENTS
SCHISTOSOMA
SKIN
SOMATIC CELLS
TRANSPLANTS
TREMATODES
TRITIUM COMPOUNDS
VERTEBRATES