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Prenatal ontogeny of lymphocyte subpopulations in pigs
Author(s) -
Marek Šinkora,
J Sinkora,
Zuzana Řeháková,
Igor Šplı́chal,
Huan Yang,
R. M. E. Parkhouse,
I Trebichavsk
Publication year - 1998
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1046/j.1365-2567.1998.00641.x
Subject(s) - biology , cd8 , ontogeny , lymphocyte , spleen , t lymphocyte , immunology , fetus , t cell , t cell receptor , phenotype , flow cytometry , immune system , microbiology and biotechnology , endocrinology , genetics , pregnancy , gene
Although porcine lymphocytes have been classified into numerous subpopulations in postnatal animals, little is known about the ontogeny of these complex cell subsets. Using double‐ and triple‐colour flow cytometry (FCM), we investigated the surface phenotype of fetal lymphoid cells in the thymus, cord blood, spleen and mesenteric lymph nodes at different stages of gestation. It was found that the major lymphocyte subpopulations started to appear at the beginning of the second third of the gestation period, with B cells being the earliest lymphocyte subpopulation to appear in the periphery. The T‐cell receptor (TCR) γδ + cells were the earliest detectable T‐cell subset, developing first in the thymus and subsequently arriving in the periphery. Later in ontogeny, however, the number of TCRαβ + lymphocytes rapidly increased, becoming the predominant T cells both in the thymus and in the periphery. Cells with the phenotype of adult natural killer cells were also identified in pig fetuses, though their nature and functional roles remain to be investigated. In addition, CD2 was expressed on most B cells whilst very few CD4 + TCRαβ + cells or CD2 + TCRγδ + cells expressed CD8, suggesting that the expression of CD2 and CD8 may reflect the functional status of the cells in postnatal animals. Taken together, this study has provided a systematic analysis of fetal porcine lymphocyte subpopulations and may provide the base for studies to establish the physiological roles of these lymphocyte subsets.