Immunocytochemical localization of substance P neurokinin-1 receptors in rat gingival tissue

Citation
Ma. Kido et al., Immunocytochemical localization of substance P neurokinin-1 receptors in rat gingival tissue, CELL TIS RE, 297(2), 1999, pp. 213-222
Citations number
39
Categorie Soggetti
Cell & Developmental Biology
Journal title
CELL AND TISSUE RESEARCH
ISSN journal
0302766X → ACNP
Volume
297
Issue
2
Year of publication
1999
Pages
213 - 222
Database
ISI
SICI code
0302-766X(199908)297:2<213:ILOSPN>2.0.ZU;2-S
Abstract
The distributions of substance P (SP) and the neurokinin-l receptor (NK1-R) , the receptor preferentially activated by SP, were examined in rat gingiva by immunocytochemical methods with light and electron microscopy. SP-immun oreactive nerve fibers were located preferentially in the junctional epithe lium (JE) but few in the other oral and oral sulcular epithelia. NK1-R immu noreactivity was found in the endothelial cells (capillaries and postcapill ary venules underlying the JE). NK1-R-labeled and -unlabeled unmyelinated n erve fibers were located close to the blood vessels and partially or comple tely covered by a Schwann cell sheath. In the JE, labeled naked axons witho ut Schwann cell sheaths were observed. Neutrophils and macrophages in the c onnective tissue underlying the JE and in the JE were also labeled with NK1 -R. Furthermore, NK1-R was found in the JE cells. Basically, immunoreaction products for NK1-R were found throughout various cells (endothelial cells, neutrophils, and JE cells) at invaginations of the plasma membrane and in vesicular and granular structures that are probably endosomes and are found close to both the plasma membrane and the nucleus. This is a first report, demonstrating the presence of NK1-R in the gingival tissue in the normal n onstimulated condition. Furthermore, it is thought that SP may modulate the permeability of blood vessels beneath the JE, the production of antimicrob ial agents in neutrophils, and the proliferation and endocytotic ability of JE cells through NK1-R.