Eotaxin is required for the baseline level of tissue eosinophils

  1. Angela N. Matthews*,
  2. Daniel S. Friend,
  3. Nives Zimmermann*,
  4. Mindy N. Sarafi,
  5. Andrew D. Luster,
  6. Eric Pearlman§,
  7. Susan E. Wert, and
  8. Marc E. Rothenberg*,
  1. *Division of Pulmonary Medicine, Allergy, and Clinical Immunology, Division of Neonatology and Pulmonary Biology, Department of Pediatrics, Children’s Hospital Medical Center, Cincinnati, OH 45229; Division of Rheumatology, Brigham and Women’s Hospital and Infectious Disease Unit, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114; and §Division of Geographic Medicine, Case Western Reserve University School of Medicine, Cleveland, OH 44106
  1. Communicated by K. Frank Austen, Harvard Medical School, Boston, MA (received for review February 2, 1998)

Abstract

Eotaxin is an eosinophil-selective chemokine that is constitutively expressed in a variety of organs such as the intestine. Previous studies have demonstrated that the recruitment of eosinophils during inflammation is partially dependent on eotaxin, but the function of constitutive eotaxin during homeostasis has not been examined. To elucidate the biological role of this molecule, we now examine tissue levels of eosinophils in healthy states in wild-type and eotaxin-deficient mice. The lamina propria of the jejunum of wild-type mice is demonstrated to express eotaxin mRNA, but not mRNA for the related monocyte chemoattractant proteins. Wild-type mice contained readily detectable eosinophils in the lamina propria of the jejunum. In contrast, mice genetically deficient in eotaxin had a large selective reduction in the number of eosinophils residing in the jejunum. The reduction of tissue eosinophils was not limited to the jejunum, because a loss of thymic eosinophils was also observed in eotaxin-deficient mice. These studies demonstrate that eotaxin is a fundamental regulator of the physiological trafficking of eosinophils during healthy states. Because a variety of chemokines are constitutively expressed, their involvement in the baseline trafficking of leukocytes into nonhematopoietic tissue should now be considered.

Footnotes

  • To whom reprint requests should be addressed at: Division of Pulmonary Medicine, Allergy, and Clinical Immunology, Department of Pediatrics, Children’s Hospital Medical Center, Cincinnati, OH 45229. e-mail: Rothm0{at}chmcc.org.

  • ABBREVIATIONS:
    MCP,
    monocyte chemoattractant protein;
    HAE,
    hematoxylin, azure II, and eosin;
    MBP,
    major basic protein
« Previous | Next Article »Table of Contents