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B cell lymphogenesis in swine is located in the bone marrow
M. Sinkora, J. Sinkorova,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1998 to 1 year ago
Freely Accessible Science Journals
from 1998-01-01 to 1 year ago
Open Access Digital Library
from 1998-01-01
- MeSH
- Cell Differentiation MeSH
- Bone Marrow Cells cytology immunology MeSH
- Antigens, CD genetics immunology MeSH
- Germ-Free Life MeSH
- Hysterectomy MeSH
- Immunophenotyping MeSH
- Histocompatibility Antigens Class II genetics immunology MeSH
- Animals, Newborn MeSH
- B-Lymphocyte Subsets cytology immunology MeSH
- Swine immunology MeSH
- Primary Cell Culture MeSH
- Immunoglobulin Heavy Chains genetics immunology MeSH
- Gene Expression Regulation, Developmental immunology MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
A course and a site of B cell development in swine are not firmly known. In this study, we show that B cell lymphogenesis is located in the bone marrow (BM). According to expression of MHC class II (MHC-II), CD2, CD21, CD25, CD45RC, CD172a, swine workshop cluster (identification number) (SWC) 7, and μHC, porcine BM cells were resolved into seven subsets representing sequential stages of development. Profile of rearrangement-specific products and transcripts from sorted BM cells confirmed the proposed developmental pathway. The same developmental pathway was further proven by analysis of selection for productive rearrangements in Ig H chains and also by cultivation studies. Cultivation also showed that earliest precursors with incomplete DJ rearrangements can still revert their B cell differentiation and develop along myeloid lineage, whereas this is impossible for later developmental stages. Proliferation and the apoptotic potential of individual developmental stages as well as critical checkpoints were also identified. Colocalization experiments showed early colocalization of MHC-II/CD2/CD172a is replaced by colocalization of MHC-II/CD2/CD21/SWC7/IgM in immature cells, whereas CD25 and CD45RC did not colocalize with any other studied molecules. In this study, we also finally prove that the BM in pigs is fully functional in adult animals and that B lymphogenesis occurs there throughout life. To our knowledge, this is the first study showing a course and a direct site of B cell lymphogenesis in swine.
References provided by Crossref.org
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