Literature DB >> 2338158

B-lymphocyte populations in Xenopus laevis.

I Hadji-Azimi1, V Coosemans, C Canicatti.   

Abstract

Two-color immunofluorescence technique was used to show the development and distribution of surface mu- cytoplasmic mu+ (s mu- c mu+) pre-B, s mu+ B- and s mu+ cIg+ plasma cells in metamorphic, postmetamorphic, and adult Xenopus. Generation of pre-B cells was evident in hematopoietic liver and spleen, but not in bone marrow, thymus, and duodenal mucosa. Surface immunoglobulin positive small lymphocytes were the most abundant in the spleen while plasma cells were detected in the thymus, duodenal mucosa, spleen, and liver. We had shown previously the appearance of s mu- c mu+ pre-B cells in the liver of Xenopus larvae at developmental stage 46 and later at stage 49 in the spleen. The frequency of pre-B cells dropped to zero at stage 58, the climax of metamorphosis. Pre-B cells start to reappear slowly as a second wave, at stage 60 through early postmetamorphic life in the liver and spleen. The percentage of surface Ig+ (sIg+) cells in the spleen of developing animals from stage 60 onward is comparable to that observed in adult life. In adult animals, the periphery of the liver continues to be active in hematopoiesis and contains some IgM producing plasma cells and rare sIg+ small lymphocytes while the pre-B cells are almost nonexistent in this region. The spleen, which is also active in some hematopoiesis, constitutes the main site of B-cell differentiation. Three ontogenic stages of pre-B, B-, and plasma cells are present in this organ. Pre-B and plasma cells are of low density and heterogeneous in size while small sIg+ B lymphocytes are of high density and much more homogeneous in size. The bone marrow in these lower anuran amphibia is rudimentary and is not a lymphopoietic tissue; in adult animals it is active only in differentiation of neutrophilic granulocytes.

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Year:  1990        PMID: 2338158     DOI: 10.1016/0145-305x(90)90009-4

Source DB:  PubMed          Journal:  Dev Comp Immunol        ISSN: 0145-305X            Impact factor:   3.636


  8 in total

1.  Distinct functional roles of amphibian (Xenopus laevis) colony-stimulating factor-1- and interleukin-34-derived macrophages.

Authors:  Leon Grayfer; Jacques Robert
Journal:  J Leukoc Biol       Date:  2015-07-01       Impact factor: 4.962

2.  Mechanisms of amphibian macrophage development: characterization of the Xenopus laevis colony-stimulating factor-1 receptor.

Authors:  Leon Grayfer; Eva-Stina Edholm; Jacques Robert
Journal:  Int J Dev Biol       Date:  2014       Impact factor: 2.203

3.  Colony-stimulating factor-1-responsive macrophage precursors reside in the amphibian (Xenopus laevis) bone marrow rather than the hematopoietic subcapsular liver.

Authors:  Leon Grayfer; Jacques Robert
Journal:  J Innate Immun       Date:  2013-03-12       Impact factor: 7.349

Review 4.  Amphibian macrophage development and antiviral defenses.

Authors:  Leon Grayfer; Jacques Robert
Journal:  Dev Comp Immunol       Date:  2015-12-15       Impact factor: 3.636

Review 5.  Comparative and developmental study of the immune system in Xenopus.

Authors:  Jacques Robert; Yuko Ohta
Journal:  Dev Dyn       Date:  2009-06       Impact factor: 3.780

6.  Evolution of immunoglobulin light chain genes: analysis of Xenopus IgL isotypes and their contribution to antibody diversity.

Authors:  J Schwager; N Bürckert; M Schwager; M Wilson
Journal:  EMBO J       Date:  1991-03       Impact factor: 11.598

Review 7.  Microbiota and mucosal immunity in amphibians.

Authors:  Bruno M Colombo; Thibault Scalvenzi; Sarah Benlamara; Nicolas Pollet
Journal:  Front Immunol       Date:  2015-03-13       Impact factor: 7.561

8.  Myelopoiesis of the Amphibian Xenopus laevis Is Segregated to the Bone Marrow, Away From Their Hematopoietic Peripheral Liver.

Authors:  Amulya Yaparla; Phillip Reeves; Leon Grayfer
Journal:  Front Immunol       Date:  2020-01-22       Impact factor: 7.561

  8 in total

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