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Osteotropic agents induce the differential secretion of granulocyte‐macrophage colony‐stimulating factor by the osteoblast cell line MC3T3‐E1
Author(s) -
Horowitz Mark C.,
Coleman David L.,
Ryaby James T.,
Einhorn Thomas A.
Publication year - 1989
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1002/jbmr.5650040616
Subject(s) - osteoblast , parathyroid hormone , secretion , haematopoiesis , bone resorption , medicine , microbiology and biotechnology , endocrinology , cell culture , osteoclast , granulocyte macrophage colony stimulating factor , chemistry , biology , cytokine , in vitro , stem cell , calcium , biochemistry , receptor , genetics
Osteoblasts play a central role in the regulation of bone remodeling. Not only are they responsible for the formation of new bone, but they also regulate bone resorption. These cells also exert regulatory influences outside the bone in that they are able to regulate hematopoiesis. However, obtaining pure populations of osteoblasts devoid of contaminating cell types remains problematic. One approach to this problem is the use of cloned osteoblastic cell lines. To this end we have used MC3T3‐E1, a cloned murine osteoblast cell line of C57BL/6 origin. We report that MC3T3‐E1 cells respond to lipopolysaccharide (LPS) and, to a lesser extent, parathyroid hormone (PTH) by the secretion of granulocyte‐macrophage colony‐stimulating factor (GM‐CSF). However, 1,25‐(OH) 2 D 3 , a potent activator of osteoblasts, fails to induce these cells to secrete GM‐CSF. These results suggest that MC3T3‐E1 cells respond to osteotropic agents in a hierarchical fashion. Secretion of GM‐CSF is not constitutive but rather requires active induction of the cells. MC3T3 cells fail to secrete detectable levels of interleukin‐2 (IL‐2), IL‐3, or IL‐4, regardless of whether or not the cells are activated. The data indicate that MC3T3‐E1 cells secrete cytokines in response to osteotropic agents in a way similar to that of normal primary osteoblasts. Therefore, MC3T3‐E1 cells may serve as a good in vitro model for primary osteoblasts.