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Volume 37, Issue 12, Pages 1400-1410 (December 2009)


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Bone marrow engraftment but limited expansion of hematopoietic cells from multipotent germline stem cells derived from neonatal mouse testis

Momoko YoshimotoabCorresponding Author Informationemail address, Toshio Heikea, Hsi Changa, Mito Kanatsu-Shinoharac, Shiro Babaa, Joseph T. Varnaub, Takashi Shinoharac, Mervin C. Yoderb, Tatsutoshi Nakahataa

Received 28 March 2009; received in revised form 1 September 2009; accepted 21 September 2009. published online 25 September 2009.

Objective

Multipotent germline stem (mGS) cells derived from neonatal mouse testis, similar to embryonic stem (ES) cells, differentiate into various types of somatic cells in vitro and produce teratomas after inoculation into mice. In the present work, we examined mGS cells for hematopoietic progenitor potential in vitro and in vivo.

Materials and Methods

mGS cells were differentiated on OP9 stromal cells and induced into Flk1+ cells. Flk1+ cells were sorted and replated on OP9 stromal cells with various cytokines and emerging hematopoietic cells were analyzed for lineage marker expression by fluorescein-activated cell sorting, progenitor activity by colony assay, and stem cell transplantation assay.

Results

mGS cells, like ES cells, produce hematopoietic progenitors, including both primitive and definitive erythromyeloid, megakaryocyte, and B- and T-cell lineages via Flk1+ progenitors. When transplanted into the bone marrow (BM) of nonobese diabetic/severe combined immunodeficient (NOD/SCID) γcnull mice directly, mGS-derived green fluorescent protein (GFP)-positive cells were detected 4 months later in the BM and spleen. GFP+ donor cells were also identified in the Hoechst33342 side population, a feature of hematopoietic stem cells. However, these mGS-derived hematopoietic cells did not proliferate in vivo, even after exposure to hematopoietic stressors, such as 5-fluorouracil (5FU) injection or serial transplantation.

Conclusion

mGS cells produced multipotent hematopoietic progenitor cells with myeloid and lymphoid lineage potential in vitro and localized in the BM after intra-BM injection but, like ES cells, failed to expand or show stem cell repopulating ability in vivo.

a Department of Pediatrics, Kyoto University, Kyoto, Japan

b Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Ind., USA

c Molecular Genetics, Graduate School of Medicine, Kyoto University, Kyoto, Japan

Corresponding Author InformationOffprint requests to: Momoko Yoshimoto, M.D., Ph.D., Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA

PII: S0301-472X(09)00368-3

doi:10.1016/j.exphem.2009.09.006


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