Chondrocyte clusters adjacent to sites of cartilage degeneration have characteristics of progenitor cells.
Chondrocyte clusters adjacent to sites of cartilage degeneration have characteristics of progenitor cells.
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DOI:
10.1002/jor.22782
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发表时间:
2015-04
影响因子:
2.8
通讯作者:
Neo, Masashi
中科院分区:
文献类型:
--
作者:
Hoshiyama, Yoshiaki;Otsuki, Shuhei;Oda, Shuhei;Kurokawa, Yoshitaka;Nakajima, Mikio;Jotoku, Tsuyoshi;Tamura, Ryuichi;Okamoto, Yoshinori;Lotz, Martin K.;Neo, Masashi
The purpose of this study was to investigate the site-specific expression pattern and the role of chondrocyte clusters in human OA knee. Cartilage explants were obtained from 45 varus knees of medial and lateral femoral condyle undergoing total knee replacement surgery. Cartilage degeneration, number of chondrocytes, and the cell arrangement were evaluated by live/dead assay and immunohistochemical analyses with antibodies of STRO-1, FGF2, and Ki-67. Chondrocytes from medial and lateral femoral condyle were cultured to compare the potential of cell proliferation and production of cartilaginous nodules. Finally, cartilage tissue from medial femoral condyle, which included cartilage cleft with chondrocyte clusters, was observed the histological alternation. As the results, chondrocyte density adjacent to severe cartilage degeneration was highest, whereas chondrocytes in lateral femoral condyle displayed low density with single type of cells. Over 80% of these chondrocyte clusters were survived, expressing STRO-1, FGF2, and Ki-67. Furthermore, chondrocyte clusters proliferated faster and produced more cartilaginous nodules than single type of chondrocytes. Cartilage clefts involving numerous chondrocyte clusters were filled with extracellular matrix during organ culture. In conclusion, chondrocyte clusters adjacent to severe cartilage degeneration have shown completely specific characteristics with progenitor and proliferative potential. Regulating chondrocyte clusters may offer new approaches to cartilage repair and OA therapy in the future.
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影响因子:
--
作者:
Lotz, Martin K.;Otsuki, Shuhei;Grogan, Shawn P.;Sah, Robert;Terkeltaub, Robert;D'Lima, Darryl
通讯作者:
D'Lima, Darryl
影响因子:
7
作者:
Chang, C;Lauffenburger, DA;Morales, TI
通讯作者:
Morales, TI
影响因子:
--
作者:
Jones, EA;Kinsey, SE;McGonagle, D
通讯作者:
McGonagle, D
DOI:
10.1016/j.bbrc.2006.02.171
发表时间:
2006-05-05
影响因子:
3.1
作者:
Chiou, M;Xu, Y;Longaker, MT
通讯作者:
Longaker, MT
影响因子:
4.9
作者:
Grogan SP;Miyaki S;Asahara H;D'Lima DD;Lotz MK
通讯作者:
Lotz MK