Mechanisms of neutropenia involving myeloid maturation arrest in burn sepsis

Ann Surg. 1998 Jul;228(1):112-22. doi: 10.1097/00000658-199807000-00017.

Abstract

Objective: To determine the mechanisms that lead to the decrease in bone marrow production of neutrophils during burn sepsis.

Summary background data: Impaired bone marrow granulopoiesis during burn sepsis often results in neutropenia despite elevated circulating levels of granulocyte colony-stimulating factor (G-CSF). To date, neither the specific stages of neutrophil maturation involved in the bone marrow suppression nor the mechanisms for the impairment have been determined.

Methods: Peripheral blood absolute neutrophil count and G-CSF levels were determined in mice 3 days after randomization to control, burn alone, or burn plus a topical inoculation of Pseudomonas aeruginosa (1000 colony-forming units). Bone marrow aspirates were analyzed for their neutrophil differentiation patterns by Gr-1 antigen expression and their G-CSF receptor status. Histologic analysis of liver, lung, spleen, and wound site was performed.

Results: In burn sepsis, absolute neutrophil count was reduced whereas plasma G-CSF levels were elevated, and myeloid differentiation was significantly shifted toward the immature mitotic myeloid cells. Bone marrow G-CSF receptor mRNA levels and G-CSF-stimulated proliferation were substantially decreased in burn sepsis. Histologic analysis revealed no significant neutrophil infiltration into the tissues.

Conclusions: In thermal injury with superimposed sepsis, neutropenia and myeloid maturation arrest, despite the elevated levels of G-CSF, correlate with the reduction in bone marrow G-CSF receptor expression. These observations may provide a potential mechanism for neutropenia in sepsis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, Surface / metabolism
  • Bone Marrow / physiopathology*
  • Burns / complications
  • Burns / pathology
  • Burns / physiopathology*
  • Evaluation Studies as Topic
  • Flow Cytometry
  • Granulocyte Colony-Stimulating Factor / blood
  • Leukocyte Count
  • Lung / pathology
  • Male
  • Mice
  • Mice, Inbred Strains
  • Neutropenia*
  • Peroxidase / metabolism
  • RNA, Messenger / analysis
  • Random Allocation
  • Receptors, Granulocyte Colony-Stimulating Factor / metabolism
  • Sepsis / etiology
  • Sepsis / pathology
  • Sepsis / physiopathology*

Substances

  • Antigens, Surface
  • RNA, Messenger
  • Receptors, Granulocyte Colony-Stimulating Factor
  • Granulocyte Colony-Stimulating Factor
  • Peroxidase