Literature DB >> 7275172

Selective localization of mesenteric lymphoblasts in mucosal tissues: effects of altering the number of donor lymphoblasts.

S E Mirski, M R McDermott, A D Befus, J Bienenstock.   

Abstract

We have studied the effect of altering the numbers of lymphoblasts from the mesenteric lymph node (MLN) transferred into syngeneic female CBA/J mice on their distribution and abundance 24 hr later. The frequency of [3H]-thymidine-labelled donor MLN cells in the recipient small intestine and lungs was directly related to the numbers transferred. Of the donor MLN lymphoblasts in the small intestine, 62.5% +/- 0.9% were seen in the basal lamina propria, 32.5% +/- 0.9% in the villus lamina propria and 5% +/- 0.6% in the epithelium. Of the MLN lymphoblasts localizing in the lungs, 90% +/- 2.3% were in the parenchyma while 6.7% +/- 1.8% and 3.3% +/- 1.0% appeared in the bronchus-associated lymphoid tissue (BALT) and the bronchial epithelium, respectively. Although few peripheral lymph node (PLN)- derived lymphoblasts localized in the small intestine, the numbers of PLN lymphoblasts in the lungs were similar to those observed after transfer of comparable doses of MLN lymphoblasts. However, PLN Lymphoblasts were found only in the pulmonary parenchyma and did not appear in either BALT or bronchial epithelium. These data suggest that the number of MLN, but likely not PLN, lymphoblasts in the circulation, directly influences the numbers of lymphoblasts which localize in intestinal mucosa, BAlt and bronchial epithelium. Even at the highest doses of MLN lymphoblasts transferred we could not saturate the capacity of these tissues to accommodate MLN lymphoblasts nor was their intra-intestinal distribution altered.

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Year:  1981        PMID: 7275172      PMCID: PMC1555085     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  14 in total

1.  Functional architecture of bronchial associated lymphoid tissue and lymphoepithelium in pulmonary cell-mediated reactions in the rabbit.

Authors:  P Rácz; K Tenner-Rácz; Q N Myrvik; L K Fainter
Journal:  J Reticuloendothel Soc       Date:  1977-07

2.  Bronchial lymphoid tissue. II. Functional characterisitics.

Authors:  J Bienenstock; N Johnston; D Y Perey
Journal:  Lab Invest       Date:  1973-06       Impact factor: 5.662

3.  Circulating T and B lymphocytes of the mouse. I. Migratory properties.

Authors:  J Sprent
Journal:  Cell Immunol       Date:  1973-04       Impact factor: 4.868

4.  Evidence for a common mucosal immunologic system. I. Migration of B immunoblasts into intestinal, respiratory, and genital tissues.

Authors:  M R McDermott; J Bienenstock
Journal:  J Immunol       Date:  1979-05       Impact factor: 5.422

5.  A comparative study of the microcirculation in the guinea-pig thymus, lymph nodes and Peyer's patches.

Authors:  J N Balu
Journal:  Clin Exp Immunol       Date:  1977-02       Impact factor: 4.330

6.  Studies on the lymphocytes of sheep. III. Destination of lymph-borne immunoblasts in relation to their tissue of origin.

Authors:  J G Hall; J Hopkins; E Orlans
Journal:  Eur J Immunol       Date:  1977-01       Impact factor: 5.532

7.  The gut-associated lymphoid system: nature and properties of the large dividing cells.

Authors:  D Guy-Grand; C Griscelli; P Vassalli
Journal:  Eur J Immunol       Date:  1974-06       Impact factor: 5.532

8.  Characteristics of mesenteric lymph node cells homing to gut-associated lymphoid tissue in syngeneic mice.

Authors:  M McWilliams; J M Phillips-Quagliata; M E Lamm
Journal:  J Immunol       Date:  1975-07       Impact factor: 5.422

9.  Origin of IgA-secreting plasma cells in the mammary gland.

Authors:  M E Roux; M McWilliams; J M Phillips-Quagliata; P Weisz-Carrington; M E Lamm
Journal:  J Exp Med       Date:  1977-11-01       Impact factor: 14.307

10.  The origin and antigen-dependent distribution of IgA-containing cells in the intestine.

Authors:  A J Husband; J L Gowans
Journal:  J Exp Med       Date:  1978-11-01       Impact factor: 14.307

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