Journal
BONE
Volume 36, Issue 2, Pages 215-223Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.bone.2004.09.024
Keywords
p45 NF-E2; megakaryocytes; osteoblasts; transcription factors; anabolic
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Funding
- NIAMS NIH HHS [AR47342, AR46032, AR49109] Funding Source: Medline
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NF-E2 is a transcription factor required for megakaryocyte differentiation. The phenotype of mice deficient in p45 NF-E2 has been characterized by increased numbers of immature megakaryocytes and the absence of functional platelets. These mice also exhibited a high bone mass phenotype with up to a 6-fold increase in trabecular bone volume and a 3- to 5-fold increase in the bone formation rate. Our data indicated that both osteoblast and osteoclast numbers were increased in vivo with a 4- to 10-fold increase in osteoblast number/tissue area and approximately a 5-fold increase in osteoclast number/tissue area. Serum osteocalcin levels were also increased in NF-E2-deficient mice, corroborating the histomorphometric data and confirming that the osteoblasts were functional. Urinary cross-links levels were measured to confirm osteoclast activity. Interestingly, the increased bone was observed only in bony sites of hematopoiesis, and was not seen in flat bones such as calvariae. We showed that cells of the osteoblast lineage do not express NF-E2 mRNA. The increased bone phenotype was adoptively transferred into irradiated wild-type mice using spleen cells from NF-E2-deficient mice. These observations suggest that a megakaryocyteosteoblast interaction occurs which is anabolic for bone. (c) 2004 Elsevier Inc. All rights reserved.
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