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Expression of Keratinocyte Growth Factor and Its Receptor in Rat Tracheal Cartilage: Possible Involvement in Wound Healing of the Damaged Cartilage
Keratinocyte growth factor (KGF) is involved in the development and regeneration of a variety of tissues. To clarify the role of KGF in cartilage wound healing, we examined the expression of KGF and its receptor (KGFR) immunohistochemically in the wound healing area of rat tracheal cartilage, and th...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Japan Society of Histochemistry and Cytochemistry
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896696/ https://www.ncbi.nlm.nih.gov/pubmed/20628626 http://dx.doi.org/10.1267/ahc.10006 |
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author | Abo, Takafumi Nagayasu, Takeshi Hishikawa, Yoshitaka Tagawa, Tsutomu Nanashima, Atsushi Yamayoshi, Takatomo Matsumoto, Keitaro An, Shucai Koji, Takehiko |
author_facet | Abo, Takafumi Nagayasu, Takeshi Hishikawa, Yoshitaka Tagawa, Tsutomu Nanashima, Atsushi Yamayoshi, Takatomo Matsumoto, Keitaro An, Shucai Koji, Takehiko |
author_sort | Abo, Takafumi |
collection | PubMed |
description | Keratinocyte growth factor (KGF) is involved in the development and regeneration of a variety of tissues. To clarify the role of KGF in cartilage wound healing, we examined the expression of KGF and its receptor (KGFR) immunohistochemically in the wound healing area of rat tracheal cartilage, and the direct effect of recombinant KGF on the proliferation and differentiation of primary cultures of rat chondrocytes. KGF was found in the cytoplasm of both chondrocytes and perichondrial cells. On the other hand, KGFR was detected only in the plasma membrane of chondrocytes. Although the expression of KGF was similar in the cartilage and perichondrial area before and after injury, KGFR expression was induced after injury and limited to proliferating chondrocytes. The staining pattern of KGF and KGFR was same in the mature and the immature rat tracheal cartilage. Moreover, in vitro experiments using primary cultured chondrocytes revealed that KGF at 200 ng/ml significantly increased the number of chondrocytes (~1.5-fold), and significantly reduced acid mucopolysaccharide production. These results indicate that KGF stimulates chondrocyte proliferation, suggesting that KGF could therapeutically modulate the wound healing process in the tracheal cartilage. |
format | Text |
id | pubmed-2896696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Japan Society of Histochemistry and Cytochemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-28966962010-07-13 Expression of Keratinocyte Growth Factor and Its Receptor in Rat Tracheal Cartilage: Possible Involvement in Wound Healing of the Damaged Cartilage Abo, Takafumi Nagayasu, Takeshi Hishikawa, Yoshitaka Tagawa, Tsutomu Nanashima, Atsushi Yamayoshi, Takatomo Matsumoto, Keitaro An, Shucai Koji, Takehiko Acta Histochem Cytochem Regular Article Keratinocyte growth factor (KGF) is involved in the development and regeneration of a variety of tissues. To clarify the role of KGF in cartilage wound healing, we examined the expression of KGF and its receptor (KGFR) immunohistochemically in the wound healing area of rat tracheal cartilage, and the direct effect of recombinant KGF on the proliferation and differentiation of primary cultures of rat chondrocytes. KGF was found in the cytoplasm of both chondrocytes and perichondrial cells. On the other hand, KGFR was detected only in the plasma membrane of chondrocytes. Although the expression of KGF was similar in the cartilage and perichondrial area before and after injury, KGFR expression was induced after injury and limited to proliferating chondrocytes. The staining pattern of KGF and KGFR was same in the mature and the immature rat tracheal cartilage. Moreover, in vitro experiments using primary cultured chondrocytes revealed that KGF at 200 ng/ml significantly increased the number of chondrocytes (~1.5-fold), and significantly reduced acid mucopolysaccharide production. These results indicate that KGF stimulates chondrocyte proliferation, suggesting that KGF could therapeutically modulate the wound healing process in the tracheal cartilage. Japan Society of Histochemistry and Cytochemistry 2010-06-28 2010-04-26 /pmc/articles/PMC2896696/ /pubmed/20628626 http://dx.doi.org/10.1267/ahc.10006 Text en © 2010 The Japan Society of Histochemistry and Cytochemistry This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Regular Article Abo, Takafumi Nagayasu, Takeshi Hishikawa, Yoshitaka Tagawa, Tsutomu Nanashima, Atsushi Yamayoshi, Takatomo Matsumoto, Keitaro An, Shucai Koji, Takehiko Expression of Keratinocyte Growth Factor and Its Receptor in Rat Tracheal Cartilage: Possible Involvement in Wound Healing of the Damaged Cartilage |
title | Expression of Keratinocyte Growth Factor and Its Receptor in Rat Tracheal Cartilage: Possible Involvement in Wound Healing of the Damaged Cartilage |
title_full | Expression of Keratinocyte Growth Factor and Its Receptor in Rat Tracheal Cartilage: Possible Involvement in Wound Healing of the Damaged Cartilage |
title_fullStr | Expression of Keratinocyte Growth Factor and Its Receptor in Rat Tracheal Cartilage: Possible Involvement in Wound Healing of the Damaged Cartilage |
title_full_unstemmed | Expression of Keratinocyte Growth Factor and Its Receptor in Rat Tracheal Cartilage: Possible Involvement in Wound Healing of the Damaged Cartilage |
title_short | Expression of Keratinocyte Growth Factor and Its Receptor in Rat Tracheal Cartilage: Possible Involvement in Wound Healing of the Damaged Cartilage |
title_sort | expression of keratinocyte growth factor and its receptor in rat tracheal cartilage: possible involvement in wound healing of the damaged cartilage |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896696/ https://www.ncbi.nlm.nih.gov/pubmed/20628626 http://dx.doi.org/10.1267/ahc.10006 |
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