ENDOTOXIN-PROTECTION OF MICE. THE RELATIONSHIP TO COLONY-FORMING UNITS

Abstract

Earlier studies have shown that bacterial endotoxins increase survival of irradiated animals. Although these substances do not confer as much protection as do the classical chemical protectants, endotoxins do significantly increase survival when given either before or for a short time following irradiation. The mechanisms of endotoxin protection have not been clearly established, but earlier studies have shown that hematopoietic stimulation is involved. The present studies were designed to evaluate the effects of endotoxin on proliferative cells in the hematopoietic system. Methods have recently been devised to measure the numbers of certain proliferative cells within the bone marrow, spleen, and other hematopoietic sites. These proliferative cells are called colony-forming units (CFU's), and their numbers are estimated by counting the 'colonies' or nodules in the spleens of irradiated mice which arise either 'spontaneously' or after injection of hematopoietic cells. The present data indicate that endotoxin does not alter the radiosensitivity of endogenous splenic CFU's; the D37 for CFU's is approx. 90 R in both endotoxin-treated and control mice. When endotoxin is injected at the time which produces optimal survival, the femur content of CFU's increases approx. 2 fold; whereas, the spleen content of CFU's is increased approx. 20 fold. The increased rate of CFU's migration from the femur to the spleen in endotoxin-treated animals may contribute to the relatively greater increase in splenic CFU's.

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Document Details

Document Type
Technical Report
Publication Date
Dec 21, 1965
Accession Number
AD0630338

Entities

People

  • E. John Ainsworth
  • Gerald E. Hanks

Organizations

  • Naval Radiological Defense Laboratory

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Abstracts
  • Blood
  • Blood Cells
  • Bone Marrow
  • Bone Marrow Cells
  • Cardiovascular System
  • Cells
  • Hematopoietic Cells
  • Hematopoietic System
  • Infection
  • Leukocytes
  • Lymphatic System
  • Radiation
  • Regression Analysis
  • Sensitivity
  • Standards
  • Stem Cells

Readers

  • Immunology and Pathology