Literature DB >> 15517397

Haemopoietic progenitors in the adult mouse omentum: permanent production of B lymphocytes and monocytes.

Maria de Fátima B Pinho1, Sandra P Hurtado, Márcia C El-Cheikh, Radovan Borojevic.   

Abstract

The coelome-associated lympho-myeloid tissues, including the omentum, are derived from early embryo haemopoietic tissue of the splanchnopleura, and produce B lymphocytes and macrophages. They are reactive in pathologies involving coelomic cavities, in which they can expand in situ the cells of inflammatory infiltrates. We have addressed the question of the role of the adult omentum in permanent basal production of early lymphopoietic progenitors (pro-B/pre-B cells), through characterisation of omentum cells ex vivo, and study of their in vitro differentiation. We have shown that the murine omentum produces early haemopoietic progenitors throughout life, including B-cell progenitors prior to the Ig gene recombination expressing RAG-1 and lambda5, as well as macrophages. Their production is stroma-dependent. The omentum stroma can supply in vitro the cytokines (SDF-1alpha, Flt3 ligand and IL-7) and the molecular environment required for generation of these two cell lineages. Omentum haemopoietic progenitors are similar to those observed in foetal blood cell production, rather than to progenitors found in the adult haemopoietic tissue in the bone marrow--in terms of phenotype expression and differentiation capacity. We conclude that a primitive pattern of haemopoiesis observed in the early embryo is permanently preserved and functional in the adult omentum, providing production of cells engaged in nonspecific protection of abdominal intestinal tissue and of the coelomic cavity.

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Year:  2004        PMID: 15517397     DOI: 10.1007/s00441-004-0998-z

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  4 in total

1.  The omentum is a site of protective IgM production during intracellular bacterial infection.

Authors:  Derek D Jones; Rachael Racine; Susan T Wittmer; Louise Harston; Amber M Papillion; Lisa M Dishaw; Troy D Randall; David L Woodland; Gary M Winslow
Journal:  Infect Immun       Date:  2015-03-16       Impact factor: 3.441

2.  5T4 oncofetal antigen is expressed in high risk of relapse childhood pre-B acute lymphoblastic leukemia and is associated with a more invasive and chemotactic phenotype.

Authors:  F V Castro; O J McGinn; S Krishnan; G Marinov; J Li; A J Rutkowski; E Elkord; D J Burt; M Holland; R Vaghjiani; A Gallego; V Saha; P L Stern
Journal:  Leukemia       Date:  2012-01-23       Impact factor: 11.528

3.  A unique case of relapsed B-acute lymphoblastic leukemia/lymphoma as an isolated omental mass.

Authors:  Kanchan Kantekure; Furha Cossor; Kenneth B Miller; Monika E Pilichowska
Journal:  Case Rep Hematol       Date:  2014-10-16

Review 4.  Epigenetic Therapy as a Putative Molecular Target to Modulate B Cell Biology and Behavior in the Context of Immunological Disorders.

Authors:  Thayse Pinheiro da Costa; Marcia Cury El-Cheikh; Katia Carneiro
Journal:  J Immunol Res       Date:  2020-02-08       Impact factor: 4.818

  4 in total

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