Role of Members of the Wnt Gene Family in Human Hematopoiesis
Open Access
- 1 November 1998
- journal article
- Published by American Society of Hematology in Blood
- Vol. 92 (9) , 3189-3202
- https://doi.org/10.1182/blood.v92.9.3189
Abstract
The hematopoietic system is derived from ventral mesoderm. A number of genes that are important in mesoderm development have been identified including members of the transforming growth factor-β (TGF-β) superfamily, the fibroblast growth factor (FGF) family, and the Wnt gene family. Because TGF-β plays a pleiotropic role in hematopoiesis, we wished to determine if other genes that are important in mesoderm development, specifically members of theWnt gene family, may play a role in hematopoiesis. Three members of the Wnt gene family (Wnt-5A, Wnt-2B, and Wnt-10B) were identified and cloned from human fetal bone stromal cells. These genes are expressed to varying levels in hematopoietic cell lines derived from T cells, B cells, myeloid cells, and erythroid cells; however, only Wnt-5A was expressed in CD34+Lin− primitive progenitor cells. The in vitro biological activity of these Wnt genes on CD34+Lin− hematopoietic progenitors was determined in a feeder cell coculture system and assayed by quantitating progenitor cell numbers, CD34+ cell numbers, and numbers of differentiated cell types. The number of hematopoietic progenitor cells was markedly affected by exposure to stromal cell layers expressing Wnt genes with 10- to 20-fold higher numbers of mixed colony-forming units (CFU-MIX), 1.5- to 2.6-fold higher numbers of CFU-granulocyte macrophage (CFU-GM), and greater than 10-fold higher numbers of burst-forming units-erythroid (BFU-E) in the Wnt-expressing cocultures compared with the controls. Colony formation by cells expanded on theWnt-expressing cocultures was similar for each of the three genes, indicating similar action on primitive progenitor cells; however, Wnt-10B showed differential activity on erythroid progenitors (BFU-E) compared with Wnt-5A and Wnt-2B. Cocultures containing Wnt-10B alone or in combination with all three Wnt genes had threefold to fourfold lower BFU-E colony numbers than the Wnt-5A– or Wnt-2B–expressing cocultures. The frequency of CD34+ cells was higher inWnt-expressing cocultures and cellular morphology indicated that coculture in the presence of Wnt genes resulted in higher numbers of less differentiated hematopoietic cells and fewer mature cells than controls. These data indicate that the gene products of theWnt family function as hematopoietic growth factors, and that they may exhibit higher specificity for earlier progenitor cells. © 1998 by The American Society of Hematology.Keywords
This publication has 52 references indexed in Scilit:
- The mouse Wnt-10B gene isolated from helper T cells is widely expressed and a possible oncogene in BR6 mouse mammary tumorigenesisPublished by Elsevier ,1999
- A frizzled homolog functions in a vertebrate Wnt signaling pathwayPublished by Elsevier ,1996
- Inducing factors in Xenopus early embryosCurrent Biology, 1994
- Transforming growth factor-beta: recent progress and new challenges.The Journal of cell biology, 1992
- Release of early human hematopoietic progenitors from quiescence by antisense transforming growth factor beta 1 or Rb oligonucleotides.The Journal of Experimental Medicine, 1991
- Experimental analysis of ventral blood island hematopoiesis in Xenopus embryonic chimerasDevelopmental Biology, 1989
- Expression of the int-1 gene in transgenic mice is associated with mammary gland hyperplasia and adenocarcinomas in male and female miceCell, 1988
- Characterization of a human hematopoietic progenitor cell capable of forming blast cell containing colonies in vitro.Journal of Clinical Investigation, 1988
- Some recent advances in the chemistry and biology of transforming growth factor-beta.The Journal of cell biology, 1987
- The transforming growth factor-β system, a complex pattern of cross-reactive ligands and receptorsCell, 1987