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Effect of Metabolic State on Immune-Hemolysis of L-Positive Low Potassium (LK) Sheep Red Blood Cells by ISO-Immune Anti-L Serum and Rabbit Serum Complement
- Source :
- Immunological Communications. 2:193-212
- Publication Year :
- 1973
- Publisher :
- Informa UK Limited, 1973.
-
Abstract
- L-antigen-positive low potassium type (LK) sheep red blood cells (SRBC) metabolically depleted by (A) starvation in glucose-free media, (B) incubation in 2-deoxy-D-glucose, or (C) exposure to iodoacetamide (IAA) were more susceptible to immune-hemolysis by ovine anti-L serum and rabbit serum complement (RSC) than control LK SRBC. The magnitude of this effect depended on the concentrations of L-antiserum and RSC used. Although all three treatments leading to enhanced immune-hemolysis of LL or LM (LK) SRBC also resulted in a loss of intracellular adenosine triphosphate [ATPli, the data do not permit conclusion of a direct correlation between immune-hemolysis and [ATP]i in these cells. Restoration of [ATP]i in glucose-containing media of LK SRBC previously metabolically depleted by treatments (A) or (B) was complete within two hours; it was followed, however, by a much slower and only partial return of immune-hemolysis to control values. The depletion induced changes appear to promote binding of RSC to, and/...
- Subjects :
- Isoantigens
medicine.medical_specialty
Adenosine
Erythrocytes
Time Factors
Potassium
Immunology
chemistry.chemical_element
Iodoacetates
chemical and pharmacologic phenomena
Hemolysis
Antibodies
Absorption
chemistry.chemical_compound
Adenosine Triphosphate
Immune system
Internal medicine
medicine
Animals
Chromatin structure remodeling (RSC) complex
Antigens
Incubation
Cells, Cultured
Sheep
biology
Immune Sera
Temperature
Complement System Proteins
medicine.disease
Amides
Culture Media
Kinetics
Glucose
Endocrinology
chemistry
Starvation
Iodoacetamide
biology.protein
Binding Sites, Antibody
Rabbits
Adenosine triphosphate
Intracellular
Subjects
Details
- ISSN :
- 00900877
- Volume :
- 2
- Database :
- OpenAIRE
- Journal :
- Immunological Communications
- Accession number :
- edsair.doi.dedup.....31cec3f07b041dac02b9252e7919225b
- Full Text :
- https://doi.org/10.3109/08820137309022792