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Journal of Cellular Biochemistry

Osteoblast lineage cells expressing high levels of Runx2 enhance hematopoietic progenitor cell proliferation and function

Authors

  • Brahmananda R. Chitteti,

    1. Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana
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  • Ying-Hua Cheng,

    1. Department of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, Indiana
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  • Drew A. Streicher,

    1. Department of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, Indiana
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  • Sonia Rodriguez-Rodriguez,

    1. Department of Pediatrics, Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana
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  • Nadia Carlesso,

    1. Department of Pediatrics, Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana
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  • Edward F. Srour,

    1. Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana
    2. Department of Pediatrics, Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana
    3. Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana
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  • Melissa A. Kacena

    Corresponding author
    1. Department of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, Indiana
    2. Department of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, Indiana
    3. Department of Biomedical Engineering, Indiana University Purdue University Indianapolis, Indianapolis, Indiana
    • Assistant Professor, Department of Orthopaedic Surgery, Indiana University School of Medicine, 1120 South Drive, FH 115, Indianapolis, IN 46202.
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  • Brahmananda R. Chitteti and Ying-Hua Cheng contributed equally to this work.

Abstract

Although osteoblasts (OB) play a key role in the hematopoietic stem cell (HSC) niche, little is known as to which specific OB lineage cells are critical for the enhancement of stem and progenitor cell function. Unlike hematopoietic cells, OB cell surface phenotypic definitions are not well developed. Therefore, to determine which OB lineage cells are most important for hematopoietic progenitor cell (HPC) function, we characterized OB differentiation by gene expression and OB function, and determined whether associations existed between OB and HPC properties. OB were harvested from murine calvariae, used immediately (fresh OB) or cultured for 1, 2, or 3 weeks prior to their co-culture with LinSca1+c-kit+ (LSK) cells for 1 week. OB gene expression, alkaline phosphatase activity, calcium deposition, hematopoietic cell number fold increase, CFU fold increase, and fold increase of LinSca1+ cells were determined. As expected, HPC properties were enhanced when LSK cells were cultured with OB compared to being cultured alone. Initial alkaline phosphatase and calcium deposition levels were significantly and inversely associated with an increase in the number of LSK progeny. Final calcium deposition levels and OB culture duration were inversely associated with all HPC parameters, while Runx2 levels were positively associated with all HPC properties. Since calcium deposition is associated with OB maturation and high levels of Runx2 are associated with less mature OB lineage cells, these results suggest that less mature OB better promote HPC proliferation and function than do more mature OB. J. Cell. Biochem. 111: 284–294, 2010. © 2010 Wiley-Liss, Inc.

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