Tachykinin expression in cartilage and function in human articular chondrocyte mechanotransduction

S. J. Millward-Sadler, Alasdair MacKenzie, M. O. Wright, H. S. Lee, K. Elliott, L. Gerrard, C. E. Fiskerstrand, D. M. Salter, J. P. Quinn

Research output: Contribution to journalArticle

49 Citations (Scopus)

Abstract

Objective. To assess whether substance P and the corresponding neurokinin 1 (NK1) receptor are expressed in human articular cartilage, and whether these molecules have a role in chondrocyte mechanotransduction.

Methods. Transgenic studies, immunohistochemistry, Western blotting, and reverse transcriptase-polymerase chain reaction were used to assess the expression of the preprotachykinin (PPT) gene, substance P, and NK1 in developing mice, in adult human articular cartilage, and in human chondrocytes in culture. Chondrocytes obtained from PPT knockout mice and human articular chondrocytes were mechanically stimulated in the presence or absence of inhibitors of substance P signaling, and cell membrane potentials or relative levels of aggrecan messenger RNA (mRNA) were measured.

Results. Replacing a region of the PPT gene transcriptional site that contains a dominant repressor of the proximal promoter activity with the constitutive minimal promoter of the human beta-globin promoter allowed expression of a marker gene in areas of chondrogenesis during mouse development and in adult chondrocytes grown in culture. Adult human, articular chondrocytes expressed endogenous PPT mRNA, substance P, and the corresponding NK1 receptor in vivo and in vitro. Blockade of substance P signaling by a chemical antagonist to the NK1 receptor inhibited chondrocyte responses to mechanical stimulation.

Conclusion. Substance P is expressed in human articular cartilage and is involved in chondrocyte mechanotransduction via the NK1 receptor in an autocrine and paracrine manner. This suggests that substance P and the NK1 receptor have roles in the maintenance of articular cartilage structure and function that were previously unrecognized.

Original languageEnglish
Pages (from-to)146-156
Number of pages10
JournalArthritis & Rheumatism
Volume48
Issue number1
Early online date10 Jan 2003
DOIs
Publication statusPublished - Jan 2003

Keywords

  • preprotachykinin-A
  • cultured human chondrocytes
  • pressure-induced strain
  • substance-P
  • neurokinin-1 receptor
  • gene-expression
  • messenger-RNA
  • alpha-5-beta-1 integrin
  • human-monocytes
  • rat-brain

Cite this

Millward-Sadler, S. J., MacKenzie, A., Wright, M. O., Lee, H. S., Elliott, K., Gerrard, L., ... Quinn, J. P. (2003). Tachykinin expression in cartilage and function in human articular chondrocyte mechanotransduction. Arthritis & Rheumatism, 48(1), 146-156. https://doi.org/10.1002/art.10711

Tachykinin expression in cartilage and function in human articular chondrocyte mechanotransduction. / Millward-Sadler, S. J.; MacKenzie, Alasdair; Wright, M. O.; Lee, H. S.; Elliott, K.; Gerrard, L.; Fiskerstrand, C. E.; Salter, D. M.; Quinn, J. P.

In: Arthritis & Rheumatism, Vol. 48, No. 1, 01.2003, p. 146-156.

Research output: Contribution to journalArticle

Millward-Sadler, SJ, MacKenzie, A, Wright, MO, Lee, HS, Elliott, K, Gerrard, L, Fiskerstrand, CE, Salter, DM & Quinn, JP 2003, 'Tachykinin expression in cartilage and function in human articular chondrocyte mechanotransduction', Arthritis & Rheumatism, vol. 48, no. 1, pp. 146-156. https://doi.org/10.1002/art.10711
Millward-Sadler, S. J. ; MacKenzie, Alasdair ; Wright, M. O. ; Lee, H. S. ; Elliott, K. ; Gerrard, L. ; Fiskerstrand, C. E. ; Salter, D. M. ; Quinn, J. P. / Tachykinin expression in cartilage and function in human articular chondrocyte mechanotransduction. In: Arthritis & Rheumatism. 2003 ; Vol. 48, No. 1. pp. 146-156.
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abstract = "Objective. To assess whether substance P and the corresponding neurokinin 1 (NK1) receptor are expressed in human articular cartilage, and whether these molecules have a role in chondrocyte mechanotransduction.Methods. Transgenic studies, immunohistochemistry, Western blotting, and reverse transcriptase-polymerase chain reaction were used to assess the expression of the preprotachykinin (PPT) gene, substance P, and NK1 in developing mice, in adult human articular cartilage, and in human chondrocytes in culture. Chondrocytes obtained from PPT knockout mice and human articular chondrocytes were mechanically stimulated in the presence or absence of inhibitors of substance P signaling, and cell membrane potentials or relative levels of aggrecan messenger RNA (mRNA) were measured.Results. Replacing a region of the PPT gene transcriptional site that contains a dominant repressor of the proximal promoter activity with the constitutive minimal promoter of the human beta-globin promoter allowed expression of a marker gene in areas of chondrogenesis during mouse development and in adult chondrocytes grown in culture. Adult human, articular chondrocytes expressed endogenous PPT mRNA, substance P, and the corresponding NK1 receptor in vivo and in vitro. Blockade of substance P signaling by a chemical antagonist to the NK1 receptor inhibited chondrocyte responses to mechanical stimulation.Conclusion. Substance P is expressed in human articular cartilage and is involved in chondrocyte mechanotransduction via the NK1 receptor in an autocrine and paracrine manner. This suggests that substance P and the NK1 receptor have roles in the maintenance of articular cartilage structure and function that were previously unrecognized.",
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AU - MacKenzie, Alasdair

AU - Wright, M. O.

AU - Lee, H. S.

AU - Elliott, K.

AU - Gerrard, L.

AU - Fiskerstrand, C. E.

AU - Salter, D. M.

AU - Quinn, J. P.

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N2 - Objective. To assess whether substance P and the corresponding neurokinin 1 (NK1) receptor are expressed in human articular cartilage, and whether these molecules have a role in chondrocyte mechanotransduction.Methods. Transgenic studies, immunohistochemistry, Western blotting, and reverse transcriptase-polymerase chain reaction were used to assess the expression of the preprotachykinin (PPT) gene, substance P, and NK1 in developing mice, in adult human articular cartilage, and in human chondrocytes in culture. Chondrocytes obtained from PPT knockout mice and human articular chondrocytes were mechanically stimulated in the presence or absence of inhibitors of substance P signaling, and cell membrane potentials or relative levels of aggrecan messenger RNA (mRNA) were measured.Results. Replacing a region of the PPT gene transcriptional site that contains a dominant repressor of the proximal promoter activity with the constitutive minimal promoter of the human beta-globin promoter allowed expression of a marker gene in areas of chondrogenesis during mouse development and in adult chondrocytes grown in culture. Adult human, articular chondrocytes expressed endogenous PPT mRNA, substance P, and the corresponding NK1 receptor in vivo and in vitro. Blockade of substance P signaling by a chemical antagonist to the NK1 receptor inhibited chondrocyte responses to mechanical stimulation.Conclusion. Substance P is expressed in human articular cartilage and is involved in chondrocyte mechanotransduction via the NK1 receptor in an autocrine and paracrine manner. This suggests that substance P and the NK1 receptor have roles in the maintenance of articular cartilage structure and function that were previously unrecognized.

AB - Objective. To assess whether substance P and the corresponding neurokinin 1 (NK1) receptor are expressed in human articular cartilage, and whether these molecules have a role in chondrocyte mechanotransduction.Methods. Transgenic studies, immunohistochemistry, Western blotting, and reverse transcriptase-polymerase chain reaction were used to assess the expression of the preprotachykinin (PPT) gene, substance P, and NK1 in developing mice, in adult human articular cartilage, and in human chondrocytes in culture. Chondrocytes obtained from PPT knockout mice and human articular chondrocytes were mechanically stimulated in the presence or absence of inhibitors of substance P signaling, and cell membrane potentials or relative levels of aggrecan messenger RNA (mRNA) were measured.Results. Replacing a region of the PPT gene transcriptional site that contains a dominant repressor of the proximal promoter activity with the constitutive minimal promoter of the human beta-globin promoter allowed expression of a marker gene in areas of chondrogenesis during mouse development and in adult chondrocytes grown in culture. Adult human, articular chondrocytes expressed endogenous PPT mRNA, substance P, and the corresponding NK1 receptor in vivo and in vitro. Blockade of substance P signaling by a chemical antagonist to the NK1 receptor inhibited chondrocyte responses to mechanical stimulation.Conclusion. Substance P is expressed in human articular cartilage and is involved in chondrocyte mechanotransduction via the NK1 receptor in an autocrine and paracrine manner. This suggests that substance P and the NK1 receptor have roles in the maintenance of articular cartilage structure and function that were previously unrecognized.

KW - preprotachykinin-A

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KW - alpha-5-beta-1 integrin

KW - human-monocytes

KW - rat-brain

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JO - Arthritis & Rheumatism

JF - Arthritis & Rheumatism

SN - 0004-3591

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ER -