Abstract #293
Section: Graduate Student Competition
Session: ADSA-ASAS Northeast Section Graduate Student Oral Competition
Format: Oral
Day/Time: Monday 3:15 PM–3:30 PM
Location: Wekiwa 7/8
Session: ADSA-ASAS Northeast Section Graduate Student Oral Competition
Format: Oral
Day/Time: Monday 3:15 PM–3:30 PM
Location: Wekiwa 7/8
# 293
Immune cells populate mesenteric adipose tissues of Holstein Friesian cows.
Bridget A. Aylward*1, Megan Clark1, Amanda Barnard1, Jen Wilson1, Candice Gittens1, Tanya Gressley1, Erin Brannick1, Marie Fecteau2, Robert Dyer1, 1Department of Animal and Food Sciences, College of Agricultural and Natural Resources, University of Delaware, Newark, DE, 2Department of Clinical Studies, New Bolton Center, University of Pennsylvania, School of Veterinary Medicine, Kennet Square, PA.
Key Words: immunology, adipose
Immune cells populate mesenteric adipose tissues of Holstein Friesian cows.
Bridget A. Aylward*1, Megan Clark1, Amanda Barnard1, Jen Wilson1, Candice Gittens1, Tanya Gressley1, Erin Brannick1, Marie Fecteau2, Robert Dyer1, 1Department of Animal and Food Sciences, College of Agricultural and Natural Resources, University of Delaware, Newark, DE, 2Department of Clinical Studies, New Bolton Center, University of Pennsylvania, School of Veterinary Medicine, Kennet Square, PA.
In many animal species, anti-inflammatory immune cells are normal residents of lean adipose depots and produce a barrier of related cytokines that protect against metabolic syndrome. Our objective was to determine if similar immune cells reside in mid-jejunum mesenteric adipose tissue (MAT) of randomly selected lean Holstein Friesian cows from an abattoir. Body condition scores were determined before slaughter (mean BCS = 2.74). Stromal cell fractions (SCF) were prepared from washed, minced MAT digested with type I collagenase. Following digestion and cleaning of the sample, cells were stained with bovine immune cell marker specific monoclonal antibodies expressed on macrophages, dendritic cells, T lymphocytes and T regulatory lymphocytes (T regs). Background controls consisted of cells stained with irrelevant, isotype-matched control antibodies. SCF composition was analyzed across 10,000 cells/sample using a Becton Dickson FACS Calibur Flow Cytometer. Marker specific fluorescence was compared with background fluorescence in controls by ANOVA. Marker expression is summarized in the table below. Results from this work indicate that populations of innate (macrophage and dendritic cells) and adaptive (lymphocytes and T regs) immune response cells do in fact reside in MAT of lean cows (Table 1). Furthermore, expression of MHC class II in the context of dendritic cells or macrophages and T lymphocytes suggests adaptive immune responses do occur in MAT. Subpopulations of FoxP3+ regulatory T lymphocytes were the dominant effector lymphocyte, implying that anti-inflammatory functions could contribute to MAT homeostasis in lean cows and potentially protect against development of metabolic disease.
Table 1. Presence of immune cells mesenteric adipose tissue (MAT) of Holstein Friesian cows
*Expression greater than background (P ≤ 0.05).
Presumptive cell type | Marker | Percent of SCF | |
Macrophages | CD11b (n=9) | 8.71 ± 0.75* | |
CD172 (n=8) | 12.57 ± 1.20* | ||
CD11b/CD172 (n=8) | 6.74 ± 0.84* | ||
CD3/CD11b (n=4) | 2.48 ± 0.62 | ||
Dendritic cells | MHC II (n=5) | 10.62 ± 0.86* | |
CD11c (n=9) | 9.43 ± 0.57* | ||
MHC II/CD11c (n=5) | 2.59 ± 0.52 | ||
CD11c/CD3 (n=4) | 1.76 ± 0.44 | ||
T lymphocytes | CD3 (n=17) | 8.99 ± 0.33* | |
CD8 (n=4) | 3.58 ± 0.89 | ||
CD3/CD8 (n=4) | 1.07 ± 0.27 | ||
T regulatory lymphocytes | FoxP3 (n=6) | 8.00 ± 0.56* | |
CD4/FOXP3(n=6) | 0.04 ± 0.12 |
Key Words: immunology, adipose