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Published on: October 11, 2012
Embryogenesis of the bursa of Fabricius: stem cell, microenvironment, and receptor-paracrine pathways
1Poultry Science Department, Clemson University, South Carolina 29634-0379, USA.
Insights
The bursa of Fabricius is crucial for understanding B cell origins and development. Research highlights the intraembryonic origin of stem cells and the microenvironment
Area of Science:
- Immunology
- Developmental Biology
- Cell Biology
Background:
- Lymphocyte origin theories evolved from epithelial/mesenchymal to bloodborne stem cells.
- The bursa of Fabricius serves as a key model for B cell development.
- Early embryogenesis involves stem cell entry into the bursa.
Purpose of the Study:
- To investigate the origin and differentiation of B cells within the bursa of Fabricius.
- To elucidate the role of the bursal microenvironment in B cell education.
- To explore the function of specific cell types, like bursal secretory dendritic cells (BSDCs), in B cell development.
Main Methods:
- Interspecific chimeric studies (quail and chick) to trace stem cell origins.
- Separation of bursal endodermal and mesodermal components.
- Analysis of cell interactions, including receptor-paracrine signaling and cell adhesion molecules.
Main Results:
- Stem cells enter the bursa during specific embryonic periods (quail: 7-11 days; chick: 7.5-14 days).
- Intraembryonic origin of stem cells contributing to the bursa was confirmed.
- The endoderm plays a primary role in bursa genesis, with mesoderm contributing to bud formation and BSDCs.
- Bursal secretory dendritic cells (BSDCs) exhibit unique IgG membrane association.
- A receptor-paracrine model involving B cells and BSDCs explains B cell repertoire development.
Conclusions:
- The bursa of Fabricius is a vital model for studying B cell origin and microenvironmental influences.
- Intraembryonic stem cells, interacting with a specialized microenvironment, orchestrate B cell differentiation.
- The bursal secretory dendritic cell (BSDC) and its interaction with B cells are critical for B cell repertoire expansion.
Abstract:
The bursa of Fabricius is an ideal model system to answer the plethora of questions related to the origin of B cells and microenvironmental issues leading to the education of the stem cell. Prior to the 1960s, lymphocytes were thought to be derived from epithelial or mesenchymal cells. Later work demonstrated the bloodborne nature of the stem cell contributing to B cells. Stem cells entered the bursa of quail and chicken between 7 and 11 and 7.5 and 14 d of embryogenesis, respectively. Interspecific chimeric studies, quail and chick, emphasized the intraembryonic origin and sites of the stem cell. The bloodborne and stromal cells that contribute to the microenvironment of the bursa orchestrate the events leading to B cell differentiation. The separation of the endodermal and mesodermal components of the bursa revealed a singular role for the endoderm in the genesis of the bursa but did not exclude a role for the mesoderm. A dark mesenchymal cell was shown to play a role in bud formation. This cell gave rise to the bursal secretory dendritic cell (BSDC), unique in its membrane association with IgG. A receptor-paracrine thesis has been proposed to explain the interaction between in-frame B cells and Ig-positive BSDC in the expansion of in-frame B cells and the subsequent development of the B cell repertoire. Cell adhesion molecules have been integrated into this thesis.
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