The CD markers of camel (Camelus dromedarius) milk cells during mastitis: the LPAM-1 expression is an indication of possible mucosal nature of the cellular trafficking

Res Vet Sci. 2015 Apr:99:77-81. doi: 10.1016/j.rvsc.2015.01.011. Epub 2015 Jan 23.

Abstract

Studying the cellular populations of the camel mammary glands through the expression pattern of the CD markers and adhesion molecules is a mean to define whether the cellular trafficking pathway is peripheral or mucosal nature. Camel milk cells from 8 Gram-positive and 5 Gram-negative infected camels were examined with flow cytometry using cross-reacting antibodies like, anti-CD4(+), CD8(+), WC+1(+)γδ, CD62L, CD11a(+)/CD18, LPAM-1, CXCR2. The overall results indicated high flow cytometry output of most of the CD makers. The statistical analysis of the mean percentage of the expressed CD markers has shown that CD62L, CXCR-2, LPAM-1, CD11a/CD18, CD8(+), IL-6R and CD20(+) were expressed in significant differences in either type of the infection. The LPAM-1 expression has provided further support to the notion that the lymphocyte trafficking is of the mucosal nature. The mucosal origin of cellular trafficking has important implications on the vaccine design and therapeutical approaches to mastitis.

Keywords: CD62L; Camel; LPMA-1; MAdCAM-1; Mammary glands; Mastitis; Mucosal; Saudi Arabia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • CD11a Antigen / metabolism
  • CD8 Antigens / metabolism
  • Camelus / immunology
  • Camelus / metabolism*
  • Cell Count
  • Cell Movement
  • Female
  • Flow Cytometry
  • Integrins / metabolism*
  • Linear Models
  • Mammary Glands, Animal / metabolism*
  • Mammary Glands, Animal / pathology
  • Mastitis / metabolism
  • Mastitis / pathology
  • Mastitis / veterinary*
  • Milk / cytology*
  • Milk / metabolism*
  • Mucous Membrane / metabolism
  • Mucous Membrane / pathology
  • Receptors, Interleukin-6 / metabolism
  • Receptors, Interleukin-8B / metabolism

Substances

  • Biomarkers
  • CD11a Antigen
  • CD8 Antigens
  • Integrins
  • Receptors, Interleukin-6
  • Receptors, Interleukin-8B
  • integrin alpha4beta7