Publication | Closed Access
Evidence that intermittent treatment with parathyroid hormone increases bone formation in adult rats by activation of bone lining cells.
596
Citations
1
References
1995
Year
OsteogenesisParathyroid GlandOsteoporosisOrthopaedic SurgeryBone Lining CellsBone BiologyBone Morphogenic ProteinParathyroid HormoneBone HomeostasisHealth SciencesBone HealthOsteoid PerimeterEndocrinologyCell BiologyBone MetabolismOsteocalcinIntermittent TreatmentDevelopmental BiologyPhysiologyPth TreatmentMedicine
Intermittent PTH treatment is known to increase osteoblast number and bone formation in rats. The study aimed to determine whether the rise in osteoblast number from intermittent PTH requires progenitor proliferation or activation of existing lining cells. The authors used thymidine labeling, histomorphometry, Northern blotting, and proline incorporation to assess osteoblast proliferation and activation during intermittent PTH treatment. Intermittent PTH markedly increased bone formation markers but did not increase osteoblast proliferation; instead, it rapidly activated preexisting bone lining cells to become osteoblasts.
Previous studies demonstrated that intermittent treatment with PTH increases osteoblast number and bone formation in growing and adult rats. The cellular mechanism for this increase in osteoblast number was investigated in 16-month-old female rats. Continuous [3H]thymidine infusion over a 1-week intermittent PTH [human PTH-(1-34)] treatment period was performed to determine the percentage of newly formed osteoblasts that originate from progenitor cells. To verify increases in bone formation, we performed histomorphometry and Northern blot analysis of selected bone matrix proteins. PTH treatment resulted in dramatic increases in fluorochrome-labeled perimeter (727%), osteoid perimeter (735%), osteoblast number (626%), and steady state mRNA levels of osteocalcin (946%) and type 1 collagen (> 1000%). Autoradiographic analysis of metaphyseal sections revealed no difference in the percentage of [3H]thymidine-labeled osteoblasts between PTH- and vehicle-treated groups (4.3 +/- 1.3% vs. 5.7 +/- 2.7%, respectively). Similar changes were observed in PTH-treated ovariectomized rats. As the PTH-induced increase in osteoblast number did not require proliferation of progenitor cells we carried out an additional experiment in adult ovariectomized rats to determine the onset of PTH action. Incorporation of [3H]proline in the distal femoral epiphysis of PTH-treated adult ovariectomized rats was increased within 24 h. We conclude that the rapid PTH-induced rise in bone formation did not require cell proliferation and was most likely due to activation of preexisting bone lining cells to osteoblasts.
| Year | Citations | |
|---|---|---|
Page 1
Page 1