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Mouse Naïve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets
Published on: April 16, 2015
Early intrathymic precursor cells acquire a CD4(low) phenotype
A M Michie1, J R Carlyle, J C Zúñiga-Pflücker
1Department of Immunology, University of Toronto, Ontario, Canada.
Insights
Early thymic progenitor cells (C4Dlow) can acquire CD4 surface expression passively from surrounding cells. This acquired CD4 phenotype is not an intrinsic characteristic of these progenitor cells.
Area of Science:
- Immunology
- Cell Biology
- Developmental Biology
Background:
- C4Dlow cells are the earliest lymphoid progenitor cells in the adult thymus.
- Thymic progenitors in fetal and RAG-2-deficient mice lack the characteristic CD4 low expression.
Purpose of the Study:
- To investigate the origin of CD4 low expression on thymic progenitor cells.
- To determine if CD4 expression is intrinsically present or passively acquired by C4Dlow cells.
Main Methods:
- Induced differentiation of thymocytes in RAG-2 deficient mice.
- Analysis of mixed bone marrow chimeras using CD4 deficient and wild-type cells.
- Acid treatment sensitivity assays.
Main Results:
- Differentiation of CD4+ CD8+ thymocytes in RAG-2-/- mice led to CD4 low expression on progenitor cells.
- Genetically CD4 deficient progenitor cells acquired a CD4 low phenotype in mixed chimeras.
- CD4 expression on C4Dlow cells was sensitive to acid treatment, suggesting passive acquisition.
Conclusions:
- Low-level CD4 surface expression on thymic progenitor cells is passively acquired from the thymic microenvironment.
- This acquired phenotype challenges the notion of CD4 as an integral cell surface molecule on these progenitors.
- Suggests other low-level cell surface molecule expressions may also be acquired phenotypes.
Abstract:
C4Dlow cells are a population of lymphoid lineage-restricted progenitor cells representing the earliest precursors present in the adult thymus. Paradoxically, thymic progenitors with a similar phenotype in fetal mice and adult RAG-2-deficient (RAG-2-/-) mice lack this characteristic low-level expression of CD4. We now show that radiation-induced differentiation of CD4+ CD8+ double positive thymocytes in RAG-2-/- mice results in the appearance of low levels of CD4 on thymocytes that are phenotypically identical to C4Dlow progenitor cells present in the normal adult thymus. This suggests that CD4 surface expression can be passively transferred from double positive cells to early progenitor thymocytes. Analysis of mixed bone marrow chimeras, reconstituted with hematopoietic stem cells from both CD4-/- (CD45.2) and CD4wt (CD45.1) congenic mice, revealed a CD4low phenotype on cells derived from CD4-/- bone marrow cells. Furthermore, these CD4-/- -derived "C4Dlow" progenitors were capable of reconstituting lymphocyte-depleted fetal thymi, with all thymocytes displaying a CD4-/- phenotype. This directly demonstrates that genetically CD4-deficient thymic progenitor cells can passively acquire a C4Dlow phenotype. Moreover, CD4 expression on C4Dlow progenitor thymocytes is sensitive to mild acid treatment, indicating that CD4 may not exist as an integral cell surface molecule on this thymocyte population. Our findings demonstrate that low-level CD4 surface expression can be passively acquired by intrathymic progenitor cells from the surrounding thymic microenvironment, suggesting that other cell surface molecules expressed at low levels may also result from an acquired phenotype.
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