Isolation and characterization of endosteal niche cell populations that regulate hematopoietic stem cells

Yuka Nakamura, Fumio Arai, Hiroko Iwasaki, Kentaro Hosokawa, Isao Kobayashi, Yumiko Gomei, Yoshiko Matsumoto, Hiroki Yoshihara, Toshio Suda

研究成果: Article

131 引用 (Scopus)

抄録

The endosteal niche is critical for the maintenance of hematopoietic stem cells (HSCs). However, it consists of a heterogeneous population in terms of differentiation stage and function. In this study, we characterized endosteal cell populations and examined their ability to maintain HSCs. Bone marrow endosteal cells were subdivided into immature mesenchymal cell-enriched ALCAM-Sca-1+ cells, osteoblast-enriched ALCAM +Sca-1-, and ALCAM-Sca-1- cells. We found that all 3 fractions maintained long-term reconstitution (LTR) activity of HSCs in an in vitro culture. In particular, ALCAM+Sca-1- cells significantly enhanced the LTR activity of HSCs by the up-regulation of homing-and cell adhesion-related genes in HSCs. Microarray analysis showed that ALCAM-Sca-1+ fraction highly expressed cytokine-related genes, whereas the ALCAM+Sca-1- fraction expressed multiple cell adhesion molecules, such as cadherins, at a greater level than the other fractions, indicating that the interaction between HSCs and osteoblasts via cell adhesion molecules enhanced the LTR activity of HSCs. Furthermore, we found an osteoblastic markerlow/- subpopulation in ALCAM +Sca-1- fraction that expressed cytokines, such as Angpt1 and Thpo, and stem cell marker genes. Altogether, these data suggest that multiple subsets of osteoblasts and mesenchymal progenitor cells constitute the endosteal niche and regulate HSCs in adult bone marrow.

元の言語English
ページ(範囲)1422-1432
ページ数11
ジャーナルBlood
116
発行部数9
DOI
出版物ステータスPublished - 2010 9 2

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Activated-Leukocyte Cell Adhesion Molecule
Hematopoietic Stem Cells
Stem cells
Cells
Population
Osteoblasts
Cell Adhesion Molecules
Genes
Bone
Cytokines
Cadherins
Microarray Analysis
Mesenchymal Stromal Cells
Cell adhesion
Cell Adhesion
Bone Marrow Cells
Microarrays
Cell culture
Up-Regulation
Stem Cells

ASJC Scopus subject areas

  • Hematology
  • Biochemistry
  • Cell Biology
  • Immunology
  • Medicine(all)

これを引用

Nakamura, Y., Arai, F., Iwasaki, H., Hosokawa, K., Kobayashi, I., Gomei, Y., ... Suda, T. (2010). Isolation and characterization of endosteal niche cell populations that regulate hematopoietic stem cells. Blood, 116(9), 1422-1432. https://doi.org/10.1182/blood-2009-08-239194

Isolation and characterization of endosteal niche cell populations that regulate hematopoietic stem cells. / Nakamura, Yuka; Arai, Fumio; Iwasaki, Hiroko; Hosokawa, Kentaro; Kobayashi, Isao; Gomei, Yumiko; Matsumoto, Yoshiko; Yoshihara, Hiroki; Suda, Toshio.

:: Blood, 巻 116, 番号 9, 02.09.2010, p. 1422-1432.

研究成果: Article

Nakamura, Y, Arai, F, Iwasaki, H, Hosokawa, K, Kobayashi, I, Gomei, Y, Matsumoto, Y, Yoshihara, H & Suda, T 2010, 'Isolation and characterization of endosteal niche cell populations that regulate hematopoietic stem cells', Blood, 巻. 116, 番号 9, pp. 1422-1432. https://doi.org/10.1182/blood-2009-08-239194
Nakamura Y, Arai F, Iwasaki H, Hosokawa K, Kobayashi I, Gomei Y その他. Isolation and characterization of endosteal niche cell populations that regulate hematopoietic stem cells. Blood. 2010 9 2;116(9):1422-1432. https://doi.org/10.1182/blood-2009-08-239194
Nakamura, Yuka ; Arai, Fumio ; Iwasaki, Hiroko ; Hosokawa, Kentaro ; Kobayashi, Isao ; Gomei, Yumiko ; Matsumoto, Yoshiko ; Yoshihara, Hiroki ; Suda, Toshio. / Isolation and characterization of endosteal niche cell populations that regulate hematopoietic stem cells. :: Blood. 2010 ; 巻 116, 番号 9. pp. 1422-1432.
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abstract = "The endosteal niche is critical for the maintenance of hematopoietic stem cells (HSCs). However, it consists of a heterogeneous population in terms of differentiation stage and function. In this study, we characterized endosteal cell populations and examined their ability to maintain HSCs. Bone marrow endosteal cells were subdivided into immature mesenchymal cell-enriched ALCAM-Sca-1+ cells, osteoblast-enriched ALCAM +Sca-1-, and ALCAM-Sca-1- cells. We found that all 3 fractions maintained long-term reconstitution (LTR) activity of HSCs in an in vitro culture. In particular, ALCAM+Sca-1- cells significantly enhanced the LTR activity of HSCs by the up-regulation of homing-and cell adhesion-related genes in HSCs. Microarray analysis showed that ALCAM-Sca-1+ fraction highly expressed cytokine-related genes, whereas the ALCAM+Sca-1- fraction expressed multiple cell adhesion molecules, such as cadherins, at a greater level than the other fractions, indicating that the interaction between HSCs and osteoblasts via cell adhesion molecules enhanced the LTR activity of HSCs. Furthermore, we found an osteoblastic markerlow/- subpopulation in ALCAM +Sca-1- fraction that expressed cytokines, such as Angpt1 and Thpo, and stem cell marker genes. Altogether, these data suggest that multiple subsets of osteoblasts and mesenchymal progenitor cells constitute the endosteal niche and regulate HSCs in adult bone marrow.",
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