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Variant isoforms of CD44 are required in early thymocyte development
C Schwärzler1, S Oliferenko, U Günthert
1Basel Institute for Immunology, Basel, Switzerland.
European Journal of Immunology
|October 10, 2001
Summary
Variant CD44 (CD44v) expression marks early T cell progenitors, crucial for thymic homing and development. These CD44v molecules facilitate hematopoietic progenitor interaction with thymic stroma, initiating T cell maturation.
Area of Science:
- Immunology
- Developmental Biology
- Cell Biology
Background:
- Early T cell development involves specific cell surface markers.
- CD44 is a cell surface glycoprotein found in standard (CD44s) and variant (CD44v) forms.
- The role of CD44 variant isoforms in T cell development is not fully understood.
Purpose of the Study:
- To investigate the expression and function of CD44 variant isoforms (CD44v) in early T cell development.
- To determine if CD44v plays a role in the interaction of hematopoietic progenitors with the thymus.
Main Methods:
- Utilized specific reagents for CD44 variant isoforms (CD44v).
- Analyzed cell surface marker expression on thymocytes and progenitor populations.
- Performed functional studies including fetal thymic organ cultures and progenitor cell colonization assays.
- Investigated the interaction of hematopoietic progenitor cells with thymic stroma.
Main Results:
- CD44v expression was detected on virtually all early thymocytes (CD3-CD4loCD8-), correlating with CD43 and CD117.
- CD44v was found on lymphocyte progenitor populations in fetal and adult hematopoietic tissues.
- Cells expressing CD44v efficiently populated fetal thymic stroma and developed into mature T cells.
- Anti-CD44v antibodies blocked thymocyte development in organ cultures.
- CD44v is required for initial hematopoietic progenitor-thymic stroma interaction.
Conclusions:
- CD44v is a reliable marker for early hematopoietic progenitors.
- CD44v plays a critical functional role in initiating T cell development within the thymus.
- CD44v mediates the crucial initial interaction between progenitor cells and the thymic stroma.