TY - JOUR
T1 - Production of 8-nitro-cGMP in osteocytic cells and its upregulation by parathyroid hormone and prostaglandin E 2
AU - Nagayama, Kazuhiro
AU - Miyamoto, Yoichi
AU - Kaneko, Kotaro
AU - Yoshimura, Kentaro
AU - Sasa, Kiyohito
AU - Akaike, Takaaki
AU - Fujii, Shigemoto
AU - Izumida, Eri
AU - Uyama, Risa
AU - Chikazu, Daichi
AU - Maki, Koutaro
AU - Kamijo, Ryutaro
N1 - Funding Information:
Funding information This study was supported by grants from JSPS KAKENHI (15H05016, 15K11053) and the MEXT-Supported Program for the Strategic Research Foundation at Private Universities (S1411009), as well as by the Private University Research Branding Project from MEXT of Japan.
Funding Information:
Ocy454 cells were generously provided by Dr. Paola Divieti Pajevic, Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Publisher Copyright:
© 2018, The Society for In Vitro Biology.
PY - 2019/1/15
Y1 - 2019/1/15
N2 - Osteocytes regulate bone remodeling, especially in response to mechanical loading and unloading of bone, with nitric oxide reported to play an important role in that process. In the present study, we found that 8-nitroguanosine 3′,5′-cyclic monophosphate (8-nitro-cGMP), a second messenger of nitric oxide in various types of cells, was produced by osteocytes in bone tissue as well as cultured osteocytic Ocy454 cells. The amount of 8-nitro-cGMP in Ocy454 cells increased during incubation with parathyroid hormone or prostaglandin E 2 , both of which are known to upregulate receptor activator of nuclear factor-κB ligand (RANKL) mRNA expression in osteocytes. On the other hand, exogenous 8-nitro-cGMP did not have effects on either the presence or absence of these bioactive substances. Furthermore, neither an inhibitor of nitric oxide synthase nor 8-bromo-cGMP, a cell-permeable analog of cGMP, showed remarkable effects on mRNA expression of sclerostin or RANKL. These results indicate that neither nitric oxide nor its downstream compounds, including 8-nitro-cGMP, alone are sufficient for induction of functional changes in osteocytes.
AB - Osteocytes regulate bone remodeling, especially in response to mechanical loading and unloading of bone, with nitric oxide reported to play an important role in that process. In the present study, we found that 8-nitroguanosine 3′,5′-cyclic monophosphate (8-nitro-cGMP), a second messenger of nitric oxide in various types of cells, was produced by osteocytes in bone tissue as well as cultured osteocytic Ocy454 cells. The amount of 8-nitro-cGMP in Ocy454 cells increased during incubation with parathyroid hormone or prostaglandin E 2 , both of which are known to upregulate receptor activator of nuclear factor-κB ligand (RANKL) mRNA expression in osteocytes. On the other hand, exogenous 8-nitro-cGMP did not have effects on either the presence or absence of these bioactive substances. Furthermore, neither an inhibitor of nitric oxide synthase nor 8-bromo-cGMP, a cell-permeable analog of cGMP, showed remarkable effects on mRNA expression of sclerostin or RANKL. These results indicate that neither nitric oxide nor its downstream compounds, including 8-nitro-cGMP, alone are sufficient for induction of functional changes in osteocytes.
KW - 8-Nitro-cGMP
KW - Nitric oxide
KW - Osteocytes
KW - Parathyroid hormone
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U2 - 10.1007/s11626-018-0304-0
DO - 10.1007/s11626-018-0304-0
M3 - Article
C2 - 30397855
AN - SCOPUS:85056084566
SN - 1071-2690
VL - 55
SP - 45
EP - 51
JO - In Vitro Cellular and Developmental Biology - Animal
JF - In Vitro Cellular and Developmental Biology - Animal
IS - 1
ER -