Skip to main content
The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1997 Feb 15;99(4):701–709. doi: 10.1172/JCI119214

Role of macrophage-stimulating protein and its receptor, RON tyrosine kinase, in ciliary motility.

O Sakamoto 1, A Iwama 1, R Amitani 1, T Takehara 1, N Yamaguchi 1, T Yamamoto 1, K Masuyama 1, T Yamanaka 1, M Ando 1, T Suda 1
PMCID: PMC507853  PMID: 9045873

Abstract

Macrophage-stimulating protein (MSP) is an 80-kD serum protein with homology to hepatocyte growth factor (HGF). Its receptor, RON tyrosine kinase, is a new member of the HGF receptor family. The MSP-RON signaling pathway has been implicated in the functional regulation of mononuclear phagocytes. However, the function of this pathway in other types of cells has not been elucidated. Here we show that in contrast to the HGF receptor, which was expressed at the basolateral surface, RON was localized at the apical surface of ciliated epithelia in the airways and oviduct. In addition, MSP was found in the bronchoalveolar space at biologically significant concentrations. MSP bound to RON on normal human bronchial epithelial cells with a high affinity (Kd = 0.5 nM) and induced autophosphorylation of RON. Activation of RON by MSP led to a significant increase in ciliary beat frequency of human nasal cilia. These findings indicate that the ciliated epithelium of the mucociliary transport apparatus is a novel target of MSP. Ciliary motility is critical for mucociliary transport. Our findings suggest that the MSP-RON signaling pathway is a novel regulatory system of mucociliary function and might be involved in the host defense and fertilization.

Full Text

The Full Text of this article is available as a PDF (597.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Amitani R., Wilson R., Rutman A., Read R., Ward C., Burnett D., Stockley R. A., Cole P. J. Effects of human neutrophil elastase and Pseudomonas aeruginosa proteinases on human respiratory epithelium. Am J Respir Cell Mol Biol. 1991 Jan;4(1):26–32. doi: 10.1165/ajrcmb/4.1.26. [DOI] [PubMed] [Google Scholar]
  2. Bezerra J. A., Witte D. P., Aronow B. J., Degen S. J. Hepatocyte-specific expression of the mouse hepatocyte growth factor-like protein. Hepatology. 1993 Aug;18(2):394–399. [PubMed] [Google Scholar]
  3. Bloemen P. G., van den Tweel M. C., Henricks P. A., Engels F., Wagenaar S. S., Rutten A. A., Nijkamp F. P. Expression and modulation of adhesion molecules on human bronchial epithelial cells. Am J Respir Cell Mol Biol. 1993 Dec;9(6):586–593. doi: 10.1165/ajrcmb/9.6.586. [DOI] [PubMed] [Google Scholar]
  4. Cohen G. B., Ren R., Baltimore D. Modular binding domains in signal transduction proteins. Cell. 1995 Jan 27;80(2):237–248. doi: 10.1016/0092-8674(95)90406-9. [DOI] [PubMed] [Google Scholar]
  5. Coleman D. L., Tuet I. K., Widdicombe J. H. Electrical properties of dog tracheal epithelial cells grown in monolayer culture. Am J Physiol. 1984 Mar;246(3 Pt 1):C355–C359. doi: 10.1152/ajpcell.1984.246.3.C355. [DOI] [PubMed] [Google Scholar]
  6. Crepaldi T., Pollack A. L., Prat M., Zborek A., Mostov K., Comoglio P. M. Targeting of the SF/HGF receptor to the basolateral domain of polarized epithelial cells. J Cell Biol. 1994 Apr;125(2):313–320. doi: 10.1083/jcb.125.2.313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cromwell O., Hamid Q., Corrigan C. J., Barkans J., Meng Q., Collins P. D., Kay A. B. Expression and generation of interleukin-8, IL-6 and granulocyte-macrophage colony-stimulating factor by bronchial epithelial cells and enhancement by IL-1 beta and tumour necrosis factor-alpha. Immunology. 1992 Nov;77(3):330–337. [PMC free article] [PubMed] [Google Scholar]
  8. Dey C. S., Brokaw C. J. Activation of Ciona sperm motility: phosphorylation of dynein polypeptides and effects of a tyrosine kinase inhibitor. J Cell Sci. 1991 Dec;100(Pt 4):815–824. doi: 10.1242/jcs.100.4.815. [DOI] [PubMed] [Google Scholar]
  9. Eliasson R., Mossberg B., Camner P., Afzelius B. A. The immotile-cilia syndrome. A congenital ciliary abnormality as an etiologic factor in chronic airway infections and male sterility. N Engl J Med. 1977 Jul 7;297(1):1–6. doi: 10.1056/NEJM197707072970101. [DOI] [PubMed] [Google Scholar]
  10. Fantl W. J., Johnson D. E., Williams L. T. Signalling by receptor tyrosine kinases. Annu Rev Biochem. 1993;62:453–481. doi: 10.1146/annurev.bi.62.070193.002321. [DOI] [PubMed] [Google Scholar]
  11. Gaudino G., Avantaggiato V., Follenzi A., Acampora D., Simeone A., Comoglio P. M. The proto-oncogene RON is involved in development of epithelial, bone and neuro-endocrine tissues. Oncogene. 1995 Dec 21;11(12):2627–2637. [PubMed] [Google Scholar]
  12. Gaudino G., Follenzi A., Naldini L., Collesi C., Santoro M., Gallo K. A., Godowski P. J., Comoglio P. M. RON is a heterodimeric tyrosine kinase receptor activated by the HGF homologue MSP. EMBO J. 1994 Aug 1;13(15):3524–3532. doi: 10.1002/j.1460-2075.1994.tb06659.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hamasaki T., Barkalow K., Richmond J., Satir P. cAMP-stimulated phosphorylation of an axonemal polypeptide that copurifies with the 22S dynein arm regulates microtubule translocation velocity and swimming speed in Paramecium. Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):7918–7922. doi: 10.1073/pnas.88.18.7918. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Han S., Stuart L. A., Degen S. J. Characterization of the DNF15S2 locus on human chromosome 3: identification of a gene coding for four kringle domains with homology to hepatocyte growth factor. Biochemistry. 1991 Oct 8;30(40):9768–9780. doi: 10.1021/bi00104a029. [DOI] [PubMed] [Google Scholar]
  15. Hanks S. K., Quinn A. M., Hunter T. The protein kinase family: conserved features and deduced phylogeny of the catalytic domains. Science. 1988 Jul 1;241(4861):42–52. doi: 10.1126/science.3291115. [DOI] [PubMed] [Google Scholar]
  16. Huff J. L., Jelinek M. A., Borgman C. A., Lansing T. J., Parsons J. T. The protooncogene c-sea encodes a transmembrane protein-tyrosine kinase related to the Met/hepatocyte growth factor/scatter factor receptor. Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6140–6144. doi: 10.1073/pnas.90.13.6140. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Iwama A., Okano K., Sudo T., Matsuda Y., Suda T. Molecular cloning of a novel receptor tyrosine kinase gene, STK, derived from enriched hematopoietic stem cells. Blood. 1994 Jun 1;83(11):3160–3169. [PubMed] [Google Scholar]
  18. Iwama A., Wang M. H., Yamaguchi N., Ohno N., Okano K., Sudo T., Takeya M., Gervais F., Morissette C., Leonard E. J. Terminal differentiation of murine resident peritoneal macrophages is characterized by expression of the STK protein tyrosine kinase, a receptor for macrophage-stimulating protein. Blood. 1995 Nov 1;86(9):3394–3403. [PubMed] [Google Scholar]
  19. Kauffman S. L. Cell proliferation in the mammalian lung. Int Rev Exp Pathol. 1980;22:131–191. [PubMed] [Google Scholar]
  20. Kurihara N., Iwama A., Tatsumi J., Ikeda K., Suda T. Macrophage-stimulating protein activates STK receptor tyrosine kinase on osteoclasts and facilitates bone resorption by osteoclast-like cells. Blood. 1996 May 1;87(9):3704–3710. [PubMed] [Google Scholar]
  21. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  22. Leonard E. J., Skeel A. A serum protein that stimulates macrophage movement, chemotaxis and spreading. Exp Cell Res. 1976 Oct 15;102(2):434–438. doi: 10.1016/0014-4827(76)90065-3. [DOI] [PubMed] [Google Scholar]
  23. Levine S. J., Larivée P., Logun C., Angus C. W., Shelhamer J. H. Corticosteroids differentially regulate secretion of IL-6, IL-8, and G-CSF by a human bronchial epithelial cell line. Am J Physiol. 1993 Oct;265(4 Pt 1):L360–L368. doi: 10.1152/ajplung.1993.265.4.L360. [DOI] [PubMed] [Google Scholar]
  24. Ohshiro K., Iwama A., Matsuno K., Ezaki T., Sakamoto O., Hamaguchi I., Takasu N., Suda T. Molecular cloning of rat macrophage-stimulating protein and its involvement in the male reproductive system. Biochem Biophys Res Commun. 1996 Oct 3;227(1):273–280. doi: 10.1006/bbrc.1996.1500. [DOI] [PubMed] [Google Scholar]
  25. Pawson T. Protein modules and signalling networks. Nature. 1995 Feb 16;373(6515):573–580. doi: 10.1038/373573a0. [DOI] [PubMed] [Google Scholar]
  26. Quantin B., Schuhbaur B., Gesnel M. C., Doll'e P., Breathnach R. Restricted expression of the ron gene encoding the macrophage stimulating protein receptor during mouse development. Dev Dyn. 1995 Dec;204(4):383–390. doi: 10.1002/aja.1002040405. [DOI] [PubMed] [Google Scholar]
  27. Reddel R. R., Ke Y., Gerwin B. I., McMenamin M. G., Lechner J. F., Su R. T., Brash D. E., Park J. B., Rhim J. S., Harris C. C. Transformation of human bronchial epithelial cells by infection with SV40 or adenovirus-12 SV40 hybrid virus, or transfection via strontium phosphate coprecipitation with a plasmid containing SV40 early region genes. Cancer Res. 1988 Apr 1;48(7):1904–1909. [PubMed] [Google Scholar]
  28. Ronsin C., Muscatelli F., Mattei M. G., Breathnach R. A novel putative receptor protein tyrosine kinase of the met family. Oncogene. 1993 May;8(5):1195–1202. [PubMed] [Google Scholar]
  29. Rossman C. M., Forrest J. B., Lee R. M., Newhouse A. F., Newhouse M. T. The dyskinetic cilia syndrome; abnormal ciliary motility in association with abnormal ciliary ultrastructure. Chest. 1981 Dec;80(6 Suppl):860–865. [PubMed] [Google Scholar]
  30. Rossman C. M., Forrest J. B., Lee R. M., Newhouse M. T. The dyskinetic cilia syndrome. Ciliary motility in immotile cilia syndrome. Chest. 1980 Oct;78(4):580–582. doi: 10.1378/chest.78.4.580. [DOI] [PubMed] [Google Scholar]
  31. Rutland J., Cole P. J. Non-invasive sampling of nasal cilia for measurement of beat frequency and study of ultrastructure. Lancet. 1980 Sep 13;2(8194):564–565. doi: 10.1016/s0140-6736(80)91995-9. [DOI] [PubMed] [Google Scholar]
  32. Sanderson M. J., Dirksen E. R. Mechanosensitivity of cultured ciliated cells from the mammalian respiratory tract: implications for the regulation of mucociliary transport. Proc Natl Acad Sci U S A. 1986 Oct;83(19):7302–7306. doi: 10.1073/pnas.83.19.7302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Schlessinger J., Ullrich A. Growth factor signaling by receptor tyrosine kinases. Neuron. 1992 Sep;9(3):383–391. doi: 10.1016/0896-6273(92)90177-f. [DOI] [PubMed] [Google Scholar]
  34. Shimamoto A., Kimura T., Matsumoto K., Nakamura T. Hepatocyte growth factor-like protein is identical to macrophage stimulating protein. FEBS Lett. 1993 Oct 25;333(1-2):61–66. doi: 10.1016/0014-5793(93)80375-5. [DOI] [PubMed] [Google Scholar]
  35. Singh-Kaw P., Zarnegar R., Siegfried J. M. Stimulatory effects of hepatocyte growth factor on normal and neoplastic human bronchial epithelial cells. Am J Physiol. 1995 Jun;268(6 Pt 1):L1012–L1020. doi: 10.1152/ajplung.1995.268.6.L1012. [DOI] [PubMed] [Google Scholar]
  36. Skeel A., Leonard E. J. Action and target cell specificity of human macrophage-stimulating protein (MSP). J Immunol. 1994 May 1;152(9):4618–4623. [PubMed] [Google Scholar]
  37. Skeel A., Yoshimura T., Showalter S. D., Tanaka S., Appella E., Leonard E. J. Macrophage stimulating protein: purification, partial amino acid sequence, and cellular activity. J Exp Med. 1991 May 1;173(5):1227–1234. doi: 10.1084/jem.173.5.1227. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Sonnenberg E., Meyer D., Weidner K. M., Birchmeier C. Scatter factor/hepatocyte growth factor and its receptor, the c-met tyrosine kinase, can mediate a signal exchange between mesenchyme and epithelia during mouse development. J Cell Biol. 1993 Oct;123(1):223–235. doi: 10.1083/jcb.123.1.223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Ullrich A., Schlessinger J. Signal transduction by receptors with tyrosine kinase activity. Cell. 1990 Apr 20;61(2):203–212. doi: 10.1016/0092-8674(90)90801-k. [DOI] [PubMed] [Google Scholar]
  40. Verdugo P. Ca2+-dependent hormonal stimulation of ciliary activity. Nature. 1980 Feb 21;283(5749):764–765. doi: 10.1038/283764a0. [DOI] [PubMed] [Google Scholar]
  41. Wang M. H., Cox G. W., Yoshimura T., Sheffler L. A., Skeel A., Leonard E. J. Macrophage-stimulating protein inhibits induction of nitric oxide production by endotoxin- or cytokine-stimulated mouse macrophages. J Biol Chem. 1994 May 13;269(19):14027–14031. [PubMed] [Google Scholar]
  42. Wang M. H., Iwama A., Skeel A., Suda T., Leonard E. J. The murine stk gene product, a transmembrane protein tyrosine kinase, is a receptor for macrophage-stimulating protein. Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):3933–3937. doi: 10.1073/pnas.92.9.3933. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Wang M. H., Ronsin C., Gesnel M. C., Coupey L., Skeel A., Leonard E. J., Breathnach R. Identification of the ron gene product as the receptor for the human macrophage stimulating protein. Science. 1994 Oct 7;266(5182):117–119. doi: 10.1126/science.7939629. [DOI] [PubMed] [Google Scholar]
  44. Wang M. H., Skeel A., Yoshimura T., Copeland T. D., Sakaguchi K., Leonard E. J. Antibodies to macrophage stimulating protein (MSP): specificity, epitope interactions, and immunoassay of MSP in human serum. J Leukoc Biol. 1993 Oct;54(4):289–295. doi: 10.1002/jlb.54.4.289. [DOI] [PubMed] [Google Scholar]
  45. Widdicombe J. H., Coleman D. L., Finkbeiner W. E., Tuet I. K. Electrical properties of monolayers cultured from cells of human tracheal mucosa. J Appl Physiol (1985) 1985 May;58(5):1729–1735. doi: 10.1152/jappl.1985.58.5.1729. [DOI] [PubMed] [Google Scholar]
  46. Wilson R., Pitt T., Taylor G., Watson D., MacDermot J., Sykes D., Roberts D., Cole P. Pyocyanin and 1-hydroxyphenazine produced by Pseudomonas aeruginosa inhibit the beating of human respiratory cilia in vitro. J Clin Invest. 1987 Jan;79(1):221–229. doi: 10.1172/JCI112787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Yarden Y., Ullrich A. Growth factor receptor tyrosine kinases. Annu Rev Biochem. 1988;57:443–478. doi: 10.1146/annurev.bi.57.070188.002303. [DOI] [PubMed] [Google Scholar]
  48. Yoshimura T., Yuhki N., Wang M. H., Skeel A., Leonard E. J. Cloning, sequencing, and expression of human macrophage stimulating protein (MSP, MST1) confirms MSP as a member of the family of kringle proteins and locates the MSP gene on chromosome 3. J Biol Chem. 1993 Jul 25;268(21):15461–15468. [PubMed] [Google Scholar]

Articles from Journal of Clinical Investigation are provided here courtesy of American Society for Clinical Investigation

RESOURCES