MISC

2004年

Development of the synovial membrane in the rat temporomandibular joint as demonstrated by immunocytochemistry for heat shock protein 25

Anatomical Record - Part A Discoveries in Molecular, Cellular, and Evolutionary Biology
  • Nobuyuki Ikeda
  • ,
  • Kayoko Nozawa-Inoue
  • ,
  • Ritsuo Takagi
  • ,
  • Takeyasu Maeda

279
1
開始ページ
623
終了ページ
635
記述言語
英語
掲載種別
DOI
10.1002/ar.a.20043
出版者・発行元
Wiley-Liss Inc.

The synovial lining layer of the temporomandibular joint (TMJ) consists of macrophage-like type A cells and fibroblast-like type B cells. Until now, little information has been available on the development of the synovial membrane in TMJ. In the present study we examined the development of the synovial lining layer in the rat TMJ by light- and electron-microscopic immunocytochemistry for heat shock protein (Hsp) 25, which is a useful marker for type B cells. At embryonic day 19 (E19), a few Hsp25-positive cells first appeared in the upper portion of the developing condyle. During the formation of the upper articular cavity (E21 to postnatal day 1 (P1)), a few positive cells were arranged on its surface. Immunoelectron microscopy demonstrated that these cells had ultrastructural features of fibroblast-like type B cells. In addition, some Hsp25-positive cells moved to the deep portion by extending their cytoplasmic processes toward the articular cavity at P3. At that time, the presence of typical macrophage-like type A cells in the lining layer was confirmed by immunoelectron microscopy. The slender processes of Hsp25-positive cells showed a continuous covering with the synovial surface at P7, followed by a drastic increase in the Hsp25-positive cells at P15 and later, when active jaw movement occurred. These findings suggested that the arrangement and morphological maturation of type B cells are closely related to the formation of the articular cavity in the embryonic period and the commencement of active jaw movement after birth, respectively. © 2004 Wiley-Liss, Inc.

リンク情報
DOI
https://doi.org/10.1002/ar.a.20043
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/15224404
ID情報
  • DOI : 10.1002/ar.a.20043
  • ISSN : 0003-276X
  • PubMed ID : 15224404
  • SCOPUS ID : 3042777673

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