File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1007/s00441-013-1670-2
- Scopus: eid_2-s2.0-84888297057
- PMID: 23824099
- WOS: WOS:000326116000010
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Effects of PTHrP on chondrocytes of sika deer antler
Title | Effects of PTHrP on chondrocytes of sika deer antler |
---|---|
Authors | |
Keywords | Chondrocyte Differentiation Proliferation PTHrP Sika deer antler |
Issue Date | 2013 |
Citation | Cell and Tissue Research, 2013, v. 354, n. 2, p. 451-460 How to Cite? |
Abstract | Parathyroid-hormone-related peptide (PTHrP) is an important regulator of chondrocyte differentiation in growth plates but little is known about its role in deer antler cartilage. The aim of the present study was to use the deer antler as a model to determine the possible role of PTHrP in regulating chondrocyte differentiation of deer antler. PTHrP and its receptor PTH1R mRNA were highly expressed in the perichondrium and cartilage of sika deer antler, as shown by in situ hybridization. Chondrocytes of deer antler were identified by toluidine blue staining of glycosaminoglycan and immunocytochemical staining of type II collagen (Col II). Treatment with PTHrP (1-34) reduced the expression of prehypertrophic chondrocyte marker Col IX and hypertrophic chondrocyte marker Col X. In order to confirm the mechanism of action of PTHrP, we initially examined the expression of cyclin D1, Bcl-2 and runt-related transcription factor 2 (Runx2) in sika deer antler by in situ hybridization and found that cyclin D1, Runx2 and Bcl-2 mRNA were also expressed in antler chondrocytes. Exogenous PTHrP induced the expression of cyclin D1 and Bcl-2 mRNA by various signalling pathways, whereas it inhibited Runx2 expression through PKA, p38MAPK, MEK and PI3K signalling pathways. Thus, PTHrP might promote the proliferation of antler chondrocytes and prevent their differentiation; it might furthermore influence the growth and development of sika deer antler. © 2013 Springer-Verlag Berlin Heidelberg. |
Persistent Identifier | http://hdl.handle.net/10722/334338 |
ISSN | 2023 Impact Factor: 3.2 2023 SCImago Journal Rankings: 0.965 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Guo, Bin | - |
dc.contributor.author | Wang, Shou Tang | - |
dc.contributor.author | Duan, Cui Cui | - |
dc.contributor.author | Li, Dang Dang | - |
dc.contributor.author | Tian, Xue Chao | - |
dc.contributor.author | Wang, Qu Yuan | - |
dc.contributor.author | Yue, Zhan Peng | - |
dc.date.accessioned | 2023-10-20T06:47:25Z | - |
dc.date.available | 2023-10-20T06:47:25Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Cell and Tissue Research, 2013, v. 354, n. 2, p. 451-460 | - |
dc.identifier.issn | 0302-766X | - |
dc.identifier.uri | http://hdl.handle.net/10722/334338 | - |
dc.description.abstract | Parathyroid-hormone-related peptide (PTHrP) is an important regulator of chondrocyte differentiation in growth plates but little is known about its role in deer antler cartilage. The aim of the present study was to use the deer antler as a model to determine the possible role of PTHrP in regulating chondrocyte differentiation of deer antler. PTHrP and its receptor PTH1R mRNA were highly expressed in the perichondrium and cartilage of sika deer antler, as shown by in situ hybridization. Chondrocytes of deer antler were identified by toluidine blue staining of glycosaminoglycan and immunocytochemical staining of type II collagen (Col II). Treatment with PTHrP (1-34) reduced the expression of prehypertrophic chondrocyte marker Col IX and hypertrophic chondrocyte marker Col X. In order to confirm the mechanism of action of PTHrP, we initially examined the expression of cyclin D1, Bcl-2 and runt-related transcription factor 2 (Runx2) in sika deer antler by in situ hybridization and found that cyclin D1, Runx2 and Bcl-2 mRNA were also expressed in antler chondrocytes. Exogenous PTHrP induced the expression of cyclin D1 and Bcl-2 mRNA by various signalling pathways, whereas it inhibited Runx2 expression through PKA, p38MAPK, MEK and PI3K signalling pathways. Thus, PTHrP might promote the proliferation of antler chondrocytes and prevent their differentiation; it might furthermore influence the growth and development of sika deer antler. © 2013 Springer-Verlag Berlin Heidelberg. | - |
dc.language | eng | - |
dc.relation.ispartof | Cell and Tissue Research | - |
dc.subject | Chondrocyte | - |
dc.subject | Differentiation | - |
dc.subject | Proliferation | - |
dc.subject | PTHrP | - |
dc.subject | Sika deer antler | - |
dc.title | Effects of PTHrP on chondrocytes of sika deer antler | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1007/s00441-013-1670-2 | - |
dc.identifier.pmid | 23824099 | - |
dc.identifier.scopus | eid_2-s2.0-84888297057 | - |
dc.identifier.volume | 354 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 451 | - |
dc.identifier.epage | 460 | - |
dc.identifier.eissn | 1432-0878 | - |
dc.identifier.isi | WOS:000326116000010 | - |