-
- Gober Hans-Jürgen
- Department of Cell Signaling, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University and Global Center of Excellence (GCOE) Program for International Research Center for Molecular Science in Tooth and Bone Diseases, Tokyo, Japan
-
- Takayanagi Hiroshi
- Department of Cell Signaling, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University and Global Center of Excellence (GCOE) Program for International Research Center for Molecular Science in Tooth and Bone Diseases, Tokyo, Japan
この論文をさがす
抄録
During evolution, the bony skeleton and the adaptive immune system have coevolved in vertebrate animals. The shared evolutionary origin and bone marrow microenvironments apparently provided the two systems with common molecules involved in individual cell lineage differentiation and function. In fact, the bone and immune systems share abundant molecules and regulatory mechanisms in the maintenance of physiologic function. Furthermore, dysregulated interactions between the immune and skeletal systems frequently result in pathological conditions affecting both systems. In humans, the most frequent skeletal pathologies are associated with bone loss through the excessive activity of osteoclasts. T cells represent the major regulatory players in bone destruction in inflammation. In this review we focus on the shared mechanisms and interactions between osteoclasts and T cells. Understanding these apparently different cell lineages in an integrated functional context should provide a molecular basis for developing novel therapeutic approaches to bone and inflammatory diseases.
収録刊行物
-
- Inflammation and Regeneration
-
Inflammation and Regeneration 29 (4), 239-248, 2009
一般社団法人 日本炎症・再生医学会
- Tweet
詳細情報 詳細情報について
-
- CRID
- 1390282680233403392
-
- NII論文ID
- 130004482242
- 10026093803
-
- NII書誌ID
- AA11508953
-
- ISSN
- 18808190
- 18809693
-
- NDL書誌ID
- 10452133
-
- 本文言語コード
- en
-
- データソース種別
-
- JaLC
- NDL
- Crossref
- CiNii Articles
-
- 抄録ライセンスフラグ
- 使用不可