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Intermittent administration of parathyroid hormone (1-34) stimulates matrix metalloproteinase-9 (MMP-9) expression in rat long bone
Journal of cellular biochemistry, 1998-09, Vol.70 (3), p.391-401
McClelland, P.
Onyia, J.E.
Miles, R.R.
Tu, Y.
Liang, J.
Harvey, A.K.
Chandrasekhar, S.
Hock, J.M.
Bidwell, J.P.
1998
Details
Autor(en) / Beteiligte
McClelland, P.
Onyia, J.E.
Miles, R.R.
Tu, Y.
Liang, J.
Harvey, A.K.
Chandrasekhar, S.
Hock, J.M.
Bidwell, J.P.
Titel
Intermittent administration of parathyroid hormone (1-34) stimulates matrix metalloproteinase-9 (MMP-9) expression in rat long bone
Ist Teil von
Journal of cellular biochemistry, 1998-09, Vol.70 (3), p.391-401
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
1998
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
Intermittent doses of parathyroid hormone (PTH) stimulate bone formation in animals and humans, but the molecular mechanisms underlying this phenomenon are not understood. Bone formation culminates with the expression of type I collagen, osteocalcin, and alkaline phosphatase, but genes that initiate and support the anabolic response are not known. To identify novel PTH‐regulated genes in bone during the anabolic response, we used differential display‐polymerase chain reaction (DDRT‐PCR) to analyze RNA from young male rats injected with either human PTH (1‐34) or vehicle control, once daily for 5 days. Total RNA was isolated from the distal femur metaphysis at 1, 6, and 48 h after the final injection and subjected to DDRT‐PCR. We identified three PTH‐responsive transcripts as matrix metalloproteinase‐9 (MMP‐9), creatine kinase, and the α1(I) polypeptide chain (COL1A1) of type I collagen. The concomitant upregulation of MMP‐9 and COL1A1 during bone formation was particularly intriguing. Further characterization of MMP‐9 expression revealed that it was localized to osteoblasts, osteocytes, megakaryocytes, and cells of the bone marrow in the rat distal femur metaphysis. Northern analysis for MMP‐9 expression in other tissues indicated that this transcript was present in the kidney and brain. In vitro, PTH regulated the protein synthesis of MMP‐9 by osteoblasts of the primary spongiosa. We propose that PTH may promote bone formation by mediating the subtle variation in MMP activities, thus preparing the extracellular matrix for the subsequent bone cell migration and deposition of new osteoid. J. Cell. Biochem. 70:391‐401, 1998. © 1998 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 0730-2312
eISSN: 1097-4644
DOI: 10.1002/(SICI)1097-4644(19980901)70:3<391::AID-JCB12>3.0.CO;2-O
Titel-ID: cdi_proquest_miscellaneous_73855175
Format
–
Schlagworte
Amino Acid Sequence
,
anabolic
,
Animals
,
Base Sequence
,
Blotting, Northern
,
Blotting, Western
,
bone
,
Bone Marrow Cells - drug effects
,
Bone Marrow Cells - metabolism
,
Cells, Cultured
,
Collagen - genetics
,
Collagenases - genetics
,
Creatine Kinase - genetics
,
Femur
,
Immunohistochemistry
,
Male
,
Matrix Metalloproteinase 9
,
MMP-9
,
Molecular Sequence Data
,
Organ Specificity
,
osteoblast
,
Osteoblasts - drug effects
,
Osteoblasts - metabolism
,
parathyroid hormone
,
Polymerase Chain Reaction
,
Rats
,
RNA, Messenger - metabolism
,
Space life sciences
,
Stromal Cells - drug effects
,
Stromal Cells - metabolism
,
Teriparatide - administration & dosage
,
Teriparatide - pharmacology
,
Up-Regulation
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