4.7 Article Book Chapter

Hematopoietic progenitor migration to the adult thymus

期刊

YEAR IN IMMUNOLOGY
卷 1217, 期 -, 页码 122-138

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1749-6632.2010.05881.x

关键词

thymus; bone marrow; T cells, progenitor; hematopoesis; hematopoietic stem cells

资金

  1. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [RC1HL099758, F30HL099271, R21HL086900] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R56AI059621, R01AI059621] Funding Source: NIH RePORTER
  3. NHLBI NIH HHS [HL099271, F30 HL099271, HL099758, RC1 HL099758, RC1 HL099758-02, HL086900, R21 HL086900-02, R21 HL086900] Funding Source: Medline
  4. NIAID NIH HHS [R56 AI059621, R01 AI059621, R01 AI059621-06A1, AI059621] Funding Source: Medline

向作者/读者索取更多资源

Although most hematopoietic lineages develop in the bone marrow (BM), T cells uniquely complete their development in the specialized environment of the thymus. Hematopoietic stem cells with long-term self-renewal capacity are not present in the thymus. As a result, continuous T cell development requires that BM-derived progenitors be imported into the thymus throughout adult life. The process of thymic homing begins with the mobilization of progenitors out of the BM, continues with their circulation in the bloodstream, and concludes with their settling in the thymus. This review will discuss each of these steps as they occur in the unirradiated and postirradiation scenarios, focusing on the molecular mechanisms of regulation. Improved knowledge about these early steps in T cell generation may accelerate the development of new therapeutic options in patients with impaired T cell number or function.

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