Ablation of Wntless in endosteal niches impairs lymphopoiesis rather than HSCs maintenance

Jingjing Cao, Lingling Zhang, Yong Wan, Hanjun Li, Rujiang Zhou, Heyuan Ding, Yongzhong Liu, Zhengju Yao, Xizhi Guo

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Osteoblasts and perivascular stromal cells constitute essential niches for HSC self-renewal and maintenance in the bone marrow. Wnt signaling is important to maintain HSC integrity. However, the paracrine role of Wnt proteins in osteoblasts-supported HSC maintenance and differentiation remains unclear. Here, we investigated hematopoiesis in mice with Wntless (Wls) deficiency in osteoblasts or Nestin-positive mesenchymal progenitor cells, which presumptively block Wnt secretion in osteoblasts. We detected defective B-cell lymphopoiesis and abnormal T-cell infiltration in the bone marrow of Wls mutant mice. Notably, no impact on HSC frequency and repopulation in the bone marrow was observed with the loss of osteoblastic Wls. Our findings revealed a supportive role of Wnts in osteoblasts-regulated B-cell lymphopoiesis. They also suggest a preferential niche role of osteoblastic Wnts for lymphoid cells rather than HSCs, providing new clues for the molecular nature of distinct niches occupied by different hematopoietic cells.

Original languageEnglish (US)
Pages (from-to)2650-2660
Number of pages11
JournalEuropean Journal of Immunology
Volume45
Issue number9
DOIs
StatePublished - Sep 1 2015
Externally publishedYes

Keywords

  • B cell
  • HSC maintenance
  • Osteoblast
  • T-cell infiltration
  • Wntless

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