Hostname: page-component-78c5997874-mlc7c Total loading time: 0 Render date: 2024-11-10T14:20:18.816Z Has data issue: false hasContentIssue false

Use and relevance of a bovine mammary gland explant model to study infection responses in bovine mammary tissue

Published online by Cambridge University Press:  15 September 2006

Aline Rabot
Affiliation:
Physiology Weihenstephan, TUM, Weihenstephaner Berg 3, 85 350 Freising, Germany
Olga Wellnitz
Affiliation:
Veterinary Physiology, University of Bern, Bremgartenstrasse 109a, 3012 Bern, Switzerland
Heinrich H D Meyer
Affiliation:
Physiology Weihenstephan, TUM, Weihenstephaner Berg 3, 85 350 Freising, Germany
Rupert M Bruckmaier
Affiliation:
Veterinary Physiology, University of Bern, Bremgartenstrasse 109a, 3012 Bern, Switzerland

Abstract

Our aim was to develop an explant model to define more precisely the early response of bovine mammary epithelial cells to infection. Therefore we investigated the mRNA expression encoding for some soluble immunological factors in lipopolysaccharide (LPS)-treated bovine mammary gland explants. Explants were taken out from the mammary gland of eight lactating cows after slaughter then incubated with LPS (10 μg/ml) for 6 h. The mRNA expression of α-lactalbumin (α-la), various cytokines, tumour necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6, IL-8, and two immunoglobulin receptors, the neonatal Fc receptor (FcRn) and polymeric immunoglobulin receptor (pIGR), were assessed with qPCR before and after 3 h and 6 h of LPS challenge. Both immunoglobulin receptors and α-la increased at 3 h then recovered their initial level at 6 h whereas IL-1β, IL-6 and IL-8 increased only after 6 h (P<0·05). Surprisingly, TNF-α transcripts did not show any regulation in response to the LPS treatment. We nevertheless concluded that our model was valid to examine the short-term response of mammary epithelial cell challenged with LPS.

Type
Research Article
Copyright
Proprietors of Journal of Dairy Research 2006

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)