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Updated: Aug 3, 2026

Human T Lymphocyte Isolation, Culture and Analysis of Migration In Vitro
Published on: June 2, 2010
Intrathymic T-cell migration: a combinatorial interplay of extracellular matrix and chemokines?
Wilson Savino1, Daniella A Mendes-da-Cruz, João S Silva
1Laboratory on Thymus Research, Dept of Immunology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Ave Brasil 4365, Manguinhos, 21045-900, Rio de Janeiro, Brazil. savino@gene.dbbm.fiocruz.br
Abstract:
Cell migration is crucial for intrathymic T-cell differentiation. Chemokines and extracellular matrix proteins per se induce thymocyte migration, and recent data suggest a combinatorial role for these molecules in this event. For example, thymocyte migration induced by fibronectin plus CXCL12/SDF1-alpha (stromal cell-derived factor1-alpha) is higher than that elicited by the chemokine alone. If such interactions are relevant in the thymus, abnormal expression of any of these ligands and/or their corresponding receptors will lead to defects in thymocyte migration. At least in the murine model of Chagas disease, this seems to be the case. Therefore a better knowledge of this complex biological circuitry will provide new clues for understanding thymus physiology and designing therapeutic strategies targeting developing T cells.
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Activation of Integrins
In "outside-in signaling," external factors in the extracellular space bind to exposed ligand binding sites on integrins. This causes the inactive protein to undergo a conformational change to become active. Integrins are often clustered on the cell membrane. Repetitive and regularly spaced ligand binding events provide an effective stimulus.

