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Bone marrow niches for hematopoietic stem cells.
Pereira, Ana Luísa; Galli, Serena; Nombela-Arrieta, César.
Afiliação
  • Pereira AL; Department of Medical Oncology and Hematology University Hospital and University of Zurich Zurich Switzerland.
  • Galli S; Department of Medical Oncology and Hematology University Hospital and University of Zurich Zurich Switzerland.
  • Nombela-Arrieta C; Department of Medical Oncology and Hematology University Hospital and University of Zurich Zurich Switzerland.
Hemasphere ; 8(8): e133, 2024 Aug.
Article em En | MEDLINE | ID: mdl-39086665
ABSTRACT
Hematopoietic stem cells (HSCs) are the cornerstone of the hematopoietic system. HSCs sustain the continuous generation of mature blood derivatives while self-renewing to preserve a relatively constant pool of progenitors throughout life. Yet, long-term maintenance of functional HSCs exclusively takes place in association with their native tissue microenvironment of the bone marrow (BM). HSCs have been long proposed to reside in fixed and identifiable anatomical units found in the complex BM tissue landscape, which control their identity and fate in a deterministic manner. In the last decades, tremendous progress has been made in the dissection of the cellular and molecular fabric of the BM, the structural organization governing tissue function, and the plethora of interactions established by HSCs. Nonetheless, a holistic model of the mechanisms controlling HSC regulation in their niche is lacking to date. Here, we provide an overview of our current understanding of BM anatomy, HSC localization, and crosstalk within local cellular neighborhoods in murine and human tissues, and highlight fundamental open questions on how HSCs functionally integrate in the BM microenvironment.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hemasphere Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hemasphere Ano de publicação: 2024 Tipo de documento: Article
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