TY - JOUR
T1 - Total parenteral nutrition-associated changes in mouse intestinal intraepithelial lymphocytes
AU - Kiristioglu, Irfan
AU - Antony, Paul
AU - Fan, Yongyi
AU - Forbush, Benjamin
AU - Mosley, R. Lee
AU - Yang, Hua
AU - Teitelbaum, Daniel H.
N1 - Funding Information:
Manuscript received February 5, 2001; accepted June 15, 2001. From the Section of Pediatric Surgery, Department of Surgery University of Michigan Medical School, and C. S. Mott Children’s Hospital, Ann Arbor, Michigan. Supported by NIH grant AI44076-01 and Abbott Laboratories, Hospital Division. Address for reprint requests: Dr. Daniel H. Teitelbaum, Section of Pediatric Surgery, University of Michigan Hospitals, Mott F3970, Box 0245, Ann Arbor, Michigan 48109.
PY - 2002
Y1 - 2002
N2 - Intraepithelial lymphocytes (IEL) play a major role in mucosal defense mechanisms against intraluminal foreign antigens. To address the role luminal nutrients have on the phenotype and function of the IEL, we administered total parenteral nutrition (TPN) to mice, with the absence of enteral intake. We hypothesized that administration of TPN would result in changes in the phenotype and function of the IEL. For this, we utilized a mouse model of TPN. A significant decline in the CD4+ IEL population occurred with TPN. Additionally, the CD8+, CD44+ IEL subset showed a 65% decline (P < 0.05), and the CD4+, CD44+ subset declined by 55% with TPN (P < 0.05). The CD8αβ+ population (a marker of thymic-dependence) also declined by 92% (P < 0.01) with TPN. IEL in the TPN group showed a significantly lower degree of in vitro proliferation. In conclusion, the IEL showed significant phenotypic changes with TPN including the loss of the thymic-derived population. Functionally, the IEL showed a significant decline in proliferation. Such changes demonstrate the important role luminal nutrients have on IEL phenotype and function.
AB - Intraepithelial lymphocytes (IEL) play a major role in mucosal defense mechanisms against intraluminal foreign antigens. To address the role luminal nutrients have on the phenotype and function of the IEL, we administered total parenteral nutrition (TPN) to mice, with the absence of enteral intake. We hypothesized that administration of TPN would result in changes in the phenotype and function of the IEL. For this, we utilized a mouse model of TPN. A significant decline in the CD4+ IEL population occurred with TPN. Additionally, the CD8+, CD44+ IEL subset showed a 65% decline (P < 0.05), and the CD4+, CD44+ subset declined by 55% with TPN (P < 0.05). The CD8αβ+ population (a marker of thymic-dependence) also declined by 92% (P < 0.01) with TPN. IEL in the TPN group showed a significantly lower degree of in vitro proliferation. In conclusion, the IEL showed significant phenotypic changes with TPN including the loss of the thymic-derived population. Functionally, the IEL showed a significant decline in proliferation. Such changes demonstrate the important role luminal nutrients have on IEL phenotype and function.
KW - CD4
KW - CD44
KW - CD62L
KW - CD8
KW - CD8αβ
KW - Intraepithelial lymphocytes
KW - Total parenteral nutrition
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U2 - 10.1023/A:1015066813675
DO - 10.1023/A:1015066813675
M3 - Article
C2 - 12018915
AN - SCOPUS:0036238732
SN - 0163-2116
VL - 47
SP - 1147
EP - 1157
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 5
ER -