Search Results

You are looking at 1 - 1 of 1 items for

  • Author: Micheal E Van Amburgh x
  • Refine by access: All content x
Clear All Modify Search
Stephanie R Thorn
Search for other papers by Stephanie R Thorn in
Google Scholar
PubMed
Close
,
Stig Purup Department of Animal Science, Department of Animal Health, Cornell University, 259 Morrison Hall, Ithaca, New York 14853, USA

Search for other papers by Stig Purup in
Google Scholar
PubMed
Close
,
Mogens Vestergaard Department of Animal Science, Department of Animal Health, Cornell University, 259 Morrison Hall, Ithaca, New York 14853, USA

Search for other papers by Mogens Vestergaard in
Google Scholar
PubMed
Close
,
Kris Sejrsen Department of Animal Science, Department of Animal Health, Cornell University, 259 Morrison Hall, Ithaca, New York 14853, USA

Search for other papers by Kris Sejrsen in
Google Scholar
PubMed
Close
,
Matthew J Meyer
Search for other papers by Matthew J Meyer in
Google Scholar
PubMed
Close
,
Micheal E Van Amburgh
Search for other papers by Micheal E Van Amburgh in
Google Scholar
PubMed
Close
, and
Yves R Boisclair
Search for other papers by Yves R Boisclair in
Google Scholar
PubMed
Close

In prepubertal heifers, the mammary parenchyma consists of epithelial and myoepithelial cells growing within a mammary fat pad (MFP). The MFP produces IGF-I that stimulates epithelial cell proliferation. In other species, adipose tissue expansion induces inflammation-related proteins (IRP), such as tumor necrosis factor α (TNFα), interleukin (IL)-6, IL-1β transforming growth factor β, monocyte chemoattractant protein 1 (MCP-1), and plasminogen activator inhibitor-1 (PAI-1). The MFP production of IRP may influence mammary development because they impair not only insulin but also IGF-I actions. Moreover, the MFP expansion seen with development and increased nutrition coincides with reduced parenchymal growth. Our first objective was to identify IRP capable of altering proliferation of bovine mammary epithelial cells. TNFα, but neither IL-6, IL-1β MCP-1 nor PAI-1, inhibited basal and IGF-I-stimulated proliferation in MAC-T cells and primary cells isolated from heifers. Our second objective was to determine whether MFP expression of IRP changed in a manner consistent with inhibition of parenchymal growth. MFP expression was measured from 100 to 350 kg body weight (experiment 1) or at 240 kg body weight (experiment 2) in dairy heifers offered restricted or high planes of nutrition. In experiment 1, neither nutrition nor development altered MFP expression of TNFα. Nutrition increased MCP-1 and PAI-1 but only before MFP expansion and after cessation of allometric parenchymal growth. In experiment 2, nutrition increased TNFα and PAI-1, but not MCP-1. Thus, MFP expansion increases IRP production in cattle, but this is unlikely to contribute to reduced parenchymal growth observed with development or increased nutrition.

Free access