Hepatocyte telomere shortening and senescence are general markers of human liver cirrhosis

Stefanie U. Wiemann, Ande Satyanarayana, Martina Tsahuridu, Hans L. Tillmann, Lars Zender, Juergen Klempnauer, Peer Flemming, Sonia Franco, Maria A. Blasco, Michael P. Manns, K. Lenhard Rudolph

Research output: Contribution to journalArticle

Abstract

Telomere shortening limits the number of cell divisions of primary human cells and might affect the regenerative capacity of organ systems during aging and chronic disease. To test whether the telomere hypothesis applies to human cirrhosis, the telomere length was monitored in cirrhosis induced by a broad variety of different etiologies. Telomeres were significantly shorter in cirrhosis compared with noncirrhotic samples independent of the primary etiology and independent of the age of the patients. Quantitative fluorescence in situ hybridization showed that telomere shortening was restricted to hepatocytes whereas lymphocytes and stellate cells in areas of fibrosis had significantly longer telomere reserves. Hepatocyte-specific telomere shortening correlated with senescence-associated β-galactosidase staining in 84% of the cirrhosis samples, specifically in hepatocytes, but not in stellate cells or lymphocytes. Hepatocyte telomere shortening and senescence correlated with progression of fibrosis in cirrhosis samples. This study demonstrates for the first time that cell type-specific telomere shortening and senescence are linked to progression of human cirrhosis. These findings give a novel explanation for the pathophysiology of cirrhosis, indicating that fibrotic scarring at the cirrhosis stage is a consequence of hepatocyte telomere shortening and senescence. The data imply that future therapies aiming to restore regenerative capacity during aging and chronic diseases will have to ensure efficient targeting of specific cell types within the affected organs.-Wiemann, S. U., Satyanarayana, A., Tsahuridu, M., Tillmann, H. L., Zender, L., Klempnauer, J., Flemming, P., Franco, S., Blasco, M. A., Manns, M. P., Rudolph, K. L. Hepatocyte telomere shortening and senescence are general markers of human liver cirrhosis.

Original languageEnglish (US)
Pages (from-to)935-942
Number of pages8
JournalFASEB Journal
Volume16
Issue number9
DOIs
StatePublished - 2002
Externally publishedYes

Fingerprint

Telomere Shortening
liver cirrhosis
telomeres
shortenings
Liver Cirrhosis
Liver
hepatocytes
Hepatocytes
Fibrosis
Telomere
Lymphocytes
Aging of materials
Cells
Galactosidases
fibrosis
chronic diseases
cells
Chronic Disease
etiology
lymphocytes

Keywords

  • Chronic disease
  • Fibrosis
  • Regeneration
  • Stellate cell activation
  • Telomerase

ASJC Scopus subject areas

  • Agricultural and Biological Sciences (miscellaneous)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Biochemistry
  • Cell Biology

Cite this

Wiemann, S. U., Satyanarayana, A., Tsahuridu, M., Tillmann, H. L., Zender, L., Klempnauer, J., ... Lenhard Rudolph, K. (2002). Hepatocyte telomere shortening and senescence are general markers of human liver cirrhosis. FASEB Journal, 16(9), 935-942. https://doi.org/10.1096/fj.01-0977com

Hepatocyte telomere shortening and senescence are general markers of human liver cirrhosis. / Wiemann, Stefanie U.; Satyanarayana, Ande; Tsahuridu, Martina; Tillmann, Hans L.; Zender, Lars; Klempnauer, Juergen; Flemming, Peer; Franco, Sonia; Blasco, Maria A.; Manns, Michael P.; Lenhard Rudolph, K.

In: FASEB Journal, Vol. 16, No. 9, 2002, p. 935-942.

Research output: Contribution to journalArticle

Wiemann, SU, Satyanarayana, A, Tsahuridu, M, Tillmann, HL, Zender, L, Klempnauer, J, Flemming, P, Franco, S, Blasco, MA, Manns, MP & Lenhard Rudolph, K 2002, 'Hepatocyte telomere shortening and senescence are general markers of human liver cirrhosis', FASEB Journal, vol. 16, no. 9, pp. 935-942. https://doi.org/10.1096/fj.01-0977com
Wiemann SU, Satyanarayana A, Tsahuridu M, Tillmann HL, Zender L, Klempnauer J et al. Hepatocyte telomere shortening and senescence are general markers of human liver cirrhosis. FASEB Journal. 2002;16(9):935-942. https://doi.org/10.1096/fj.01-0977com
Wiemann, Stefanie U. ; Satyanarayana, Ande ; Tsahuridu, Martina ; Tillmann, Hans L. ; Zender, Lars ; Klempnauer, Juergen ; Flemming, Peer ; Franco, Sonia ; Blasco, Maria A. ; Manns, Michael P. ; Lenhard Rudolph, K. / Hepatocyte telomere shortening and senescence are general markers of human liver cirrhosis. In: FASEB Journal. 2002 ; Vol. 16, No. 9. pp. 935-942.
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AU - Satyanarayana, Ande

AU - Tsahuridu, Martina

AU - Tillmann, Hans L.

AU - Zender, Lars

AU - Klempnauer, Juergen

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AU - Franco, Sonia

AU - Blasco, Maria A.

AU - Manns, Michael P.

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AB - Telomere shortening limits the number of cell divisions of primary human cells and might affect the regenerative capacity of organ systems during aging and chronic disease. To test whether the telomere hypothesis applies to human cirrhosis, the telomere length was monitored in cirrhosis induced by a broad variety of different etiologies. Telomeres were significantly shorter in cirrhosis compared with noncirrhotic samples independent of the primary etiology and independent of the age of the patients. Quantitative fluorescence in situ hybridization showed that telomere shortening was restricted to hepatocytes whereas lymphocytes and stellate cells in areas of fibrosis had significantly longer telomere reserves. Hepatocyte-specific telomere shortening correlated with senescence-associated β-galactosidase staining in 84% of the cirrhosis samples, specifically in hepatocytes, but not in stellate cells or lymphocytes. Hepatocyte telomere shortening and senescence correlated with progression of fibrosis in cirrhosis samples. This study demonstrates for the first time that cell type-specific telomere shortening and senescence are linked to progression of human cirrhosis. These findings give a novel explanation for the pathophysiology of cirrhosis, indicating that fibrotic scarring at the cirrhosis stage is a consequence of hepatocyte telomere shortening and senescence. The data imply that future therapies aiming to restore regenerative capacity during aging and chronic diseases will have to ensure efficient targeting of specific cell types within the affected organs.-Wiemann, S. U., Satyanarayana, A., Tsahuridu, M., Tillmann, H. L., Zender, L., Klempnauer, J., Flemming, P., Franco, S., Blasco, M. A., Manns, M. P., Rudolph, K. L. Hepatocyte telomere shortening and senescence are general markers of human liver cirrhosis.

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KW - Regeneration

KW - Stellate cell activation

KW - Telomerase

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