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Human blood and rabbit peritoneal leucocytes as sources of endogenous mediators
Abstract:
"Buffy-coat" residues from human blood have been investigated as a source of leucocytic endogenous mediator (LEM). After separation from most of the erythrocytes and uptake of opsonized zymosan by the polymorphonuclear leucocytes (PML) and macrophages, the cells were incubated in Hanks' medium. To demonstrate the presence of LEM the supernatant thus produced was injected into rats and then after 24 h increases in the plasma concentrations of haptoglobin, alpha 2 macroglobulin and fibrinogen were estimated. For comparison rats were also injected with LEM prepared from rabbit peritoneal cells. Because these cells were obtained from rabbits which had been stimulated by i.p. injection of glycogen, addition of zymosan in vitro was not required. Despite the different species from which the leucocytes were obtained and the different method of preparation of LEM, similar increases in concentration of haptoglobin, fibrinogen and alpha 2 macroglobulin in the plasma of the recipient rats were obtained. Because injection of LEM resulted in very varied increases in concentration of each of the 3 plasma proteins, an attempt was made to ascertain whether positive responses for all 3 proteins occurred in the same rats or whether the rats responded randomly. The presence of endogenous pyrogen as a constituent of the LEM produced from both sources was confirmed using both rabbits and prewarmed mice (Bodel and Miller, 1976).
Insights
Human blood "buffy-coat" yields leucocytic endogenous mediator (LEM). Injecting LEM into rats increased plasma haptoglobin, alpha 2 macroglobulin, and fibrinogen, confirming its pyrogenic properties.
Area of Science:
- Immunology
- Biochemistry
Background:
- Leucocytic endogenous mediator (LEM) is a key signaling molecule in inflammatory responses.
- Investigating novel sources and properties of LEM is crucial for understanding inflammation.
Purpose of the Study:
- To explore human "buffy-coat" residues as a source of leucocytic endogenous mediator (LEM).
- To characterize the effects of LEM on acute-phase protein concentrations in vivo.
- To confirm the presence of endogenous pyrogen within the prepared LEM.
Main Methods:
- Human "buffy-coat" cells (polymorphonuclear leucocytes and macrophages) were incubated after opsonized zymosan uptake.
- Supernatants containing LEM were injected into rats to measure plasma protein changes.
- Comparison with LEM derived from rabbit peritoneal cells was performed.
- Endogenous pyrogen presence was confirmed in rabbits and mice.
Main Results:
- Injection of LEM from human and rabbit sources induced significant increases in rat plasma haptoglobin, alpha 2 macroglobulin, and fibrinogen.
- The magnitude of protein increase varied among individual rats.
- The presence of endogenous pyrogen was confirmed in both LEM preparations.
Conclusions:
- Human "buffy-coat" is a viable source for preparing leucocytic endogenous mediator (LEM).
- LEM reliably elevates acute-phase protein levels in vivo.
- LEM contains endogenous pyrogenic activity, contributing to fever responses.