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Parenteral Feeding Depletes Pulmonary Lymphocyte Populations
Author(s) -
Hermsen Joshua L.,
Gomez F. Enrique,
Sano Yoshifumi,
Kang Woodae,
Maeshima Yoshinori,
Kudsk Kenneth A.
Publication year - 2009
Publication title -
journal of parenteral and enteral nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.935
H-Index - 98
eISSN - 1941-2444
pISSN - 0148-6071
DOI - 10.1177/0148607109332909
Subject(s) - collagenase , flow cytometry , immune system , lymphocyte , lung , t cell , t lymphocyte , cd3 , immunology , andrology , biology , microbiology and biotechnology , medicine , cd8 , biochemistry , enzyme
Background: The effect of parenteral nutrition (PN) on lymphocyte mass in the lung is unknown, but reduced mucosal lymphocytes are hypothesized to play a role in the reduced immunoglobulin A–mediated immunity in both gut and lung. The ability to transfer and track cells between mice may allow study of diet‐induced mucosal immune function. The objectives of this study are to characterize lung T‐cell populations following parenteral feeding and to study distribution patterns of transferred donor lung T cells in recipient mice. Methods: In experiment 1, cannulated male Balb/c mice are randomized to receive chow or PN for 5 days. Lung lymphocytes are obtained via collagenase digestion, and flow cytometric analysis is used to identify total T (CD3+) and B (CD45/B220+) cells. In experiment 2, isolated lung T cells from chow‐fed male Balb/c mice are pooled and labeled in vitro with a fluorescent dye (carboxyfluorescein diacetate succinimidyl ester [CFSE]), and 1.1 × 10 8 CFSE+ cells (3.1 × 10 6 T cells) are transferred to chow‐fed Balb/c recipients. Cells recovered from recipient lungs and intestinal lamina propria (LP) are analyzed by flow cytometry to determine CFSE/CD3+ T cells at 1, 2, and 7 days. In experiment 3, cells are transferred to PN‐fed recipients. Results: In experiment 1, PN significantly decreases lung T‐ and B‐cell populations compared with chow feeding. In experiment 2, CFSE+ T‐cell retention is highest on day 1 in lung and LP, and decreases on day 2. Cells are gone by day 7; 98.1% of retained donor lung T cells migrate to recipient lungs and 1.9% to the intestine on day 1. Similar results are seen in experiment 3 after transfer of cells to PN‐fed recipients. Conclusions: PN reduces pulmonary lymphocyte populations consistent with impaired respiratory immunity. Transferred lung T cells preferentially localize to recipient lungs rather than intestine with maximal accumulation at 24 hours. Limited cross‐talk of transferred lung T cells to the intestine indicates that mucosal lymphocyte traffic might be programmed to localize to specific effector sites.