Diverse osteoclastogenesis of bone marrow from mandible versus long bone.
Diverse osteoclastogenesis of bone marrow from mandible versus long bone.
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DOI:
10.1902/jop.2013.130376
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发表时间:
2014-06
影响因子:
4.3
通讯作者:
Tetradis S
中科院分区:
文献类型:
--
作者:
Chaichanasakul T;Kang B;Bezouglaia O;Aghaloo TL;Tetradis S
Mandible (MB) and maxilla possess unique metabolic and functional properties and demonstrate discrete responses to homeostatic, mechanical, hormonal and developmental stimuli. Osteogenic potential of bone marrow stromal cells (BMSCs) differs between MB versus long bones (LB). Furthermore, MB versus LB derived osteoclasts (OCs) have disparate functional properties. Here, we explored the osteoclastogenic potential of rat MB versus LB marrow in vitro and in vivo under basal and stimulated conditions. Bone marrow from rat MB and LB was cultured in osteoblastic or osteoclastic differentiation media. Tartrate resistant acid phosphatase (TRAP) staining, resorption pit assays, and real-time PCR were performed. Additionally, osmotic mini-pumps were implanted in animals, mandibles and tibiae were isolated and multinucleated cells (MNCs) were measured. MB versus LB marrow cultures differentiated with RANKL and M-CSF produced more TRAP+ multinucleated cells (MNCs) and greater resorptive area. To explore MB versus LB BMSC supported osteoclastogenesis, confluent BMSCs were cultured with parathyroid hormone (PTH), 1α,25-dihydroxyvitaminD3 (1,25D3), or PTH+1,25D3. 1,25D3 or PTH+1,25D3 treated LB BMSCs expressed significantly higher RANKL and lower OPG mRNA and increased RANKL:OPG ratio. When whole marrow was cultured with PTH+1,25D3, more TRAP+ MNCs were seen in LB versus MB cultures. Ultimately, rats were infused with PTH+1,25D3 and MB versus tibia MNCs were measured. Hormonal stimulation increased osteoclastogenesis in both MB and tibia. However, higher TRAP+ MNC numbers were observed in tibia versus MB under basal and hormonal stimulation. Collectively, our data illustrate differences both on osteoclastogenic potential and OC numbers of MB versus LB marrow.
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影响因子:
6.2
作者:
Mavropoulos, Anestis;Rizzoli, Rene;Ammann, Patrick
通讯作者:
Ammann, Patrick
影响因子:
4
作者:
MARTIN, TJ;NG, KW
通讯作者:
NG, KW
影响因子:
4.1
作者:
Akintoye, Sunday O.;Lam, Thanh;Robey, Pamela G.
通讯作者:
Robey, Pamela G.
影响因子:
2.3
作者:
de Smit, M. J.;Brouwer, E.;van Winkelhoff, A. J.
通讯作者:
van Winkelhoff, A. J.
DOI:
10.1006/bbrc.1999.0524
发表时间:
1999-04-21
影响因子:
3.1
作者:
Nagai, M;Sato, N
通讯作者:
Sato, N