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Parathyroid hormone stimulation and PKA signaling of latent transforming growth factor‐β binding protein‐1 (LTBP‐1) mRNA expression in osteoblastic cells
Author(s) -
Kwok Sukyee,
Qin Ling,
Partridge Nicola C.,
Selvamurugan Nagarajan
Publication year - 2005
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.20453
Subject(s) - parathyroid hormone , medicine , endocrinology , transforming growth factor , messenger rna , signal transduction , osteoblast , chemistry , gene expression , biology , microbiology and biotechnology , gene , calcium , in vitro , biochemistry
Parathyroid hormone (PTH) regulates bone remodeling and calcium homeostasis by acting on osteoblasts. Recently, the gene expression profile changes in the rat PTH (1–34, 10 −8 M)‐treated rat osteoblastic osteosarcoma cell line, UMR 106‐01, using DNA microarray analysis showed that mRNA for LTBP‐1, a latent transforming growth factor (TGF‐β)‐binding protein is stimulated by PTH. Latent TGF‐β binding proteins (LTBPs) are required for the proper folding and secretion of TGF‐β, thus modifying the activity of TGF‐β, which is a local factor necessary for bone remodeling. We show here by real time RT‐PCR that PTH‐stimulated LTBP‐1 mRNA expression in rat and mouse preosteoblastic cells. PTH also stimulated LTBP‐1 mRNA expression in all stages of rat primary osteoblastic cells but extended expression was found in differentiating osteoblasts. PTH also stimulated TGF‐β1 mRNA expression in rat primary osteoblastic cells, indicating a link between systemic and local factors for intracellular signaling in osteoblasts. An additive effect on LTBP‐1 mRNA expression was found when UMR 106‐01 cells were treated with PTH and TGF‐β1 together. We further examined the signaling pathways responsible for PTH‐stimulated LTBP‐1 and TGF‐β1 mRNA expression in UMR 106‐01 cells. The PTH stimulation of LTBP‐1 and TGF‐β1 mRNA expression was dependent on the PKA and the MAPK (MEK and p38 MAPK) pathways, respectively in these cells, suggesting that PTH mediates its effects on osteoblasts by several intracellular signaling pathways. Overall, we demonstrate here that PTH stimulates LTBP‐1 mRNA expression in osteoblastic cells and this is PKA‐dependent. This event may be important for PTH action via TGF‐β in bone remodeling. © 2005 Wiley‐Liss, Inc.