Abstract
Myonuclear apoptosis is an early event in the pathology of dystrophin-deficient muscular dystrophy in the mdx mouse. However, events that initiate apoptosis in muscular dystrophy are unknown, and whether elimination of apoptosis can ameliorate subsequent muscle wasting remains a major question. We have tested the hypothesis that cytotoxic T-lymphocytes initiate myonuclear apoptosis in dystrophic muscle, and examined whether perforin-mediated cytotoxicity plays a role in the pathophysiology of muscular dystrophy. Mdx mice showed muscle invasion by cytotoxic T cells and helper T cells at the onset of histologically detectable muscle fiber pathology. At this time, perforin-expressing cells were also present at elevated concentration. Mdx mice depleted of CD8(+) cells showed a significant reduction of apoptotic myonuclei concentration and a reduction in necrosis, judged by macrophage invasion of muscle fibers. Double-mutant mice, deficient in dystrophin and perforin, showed nearly complete absence of myonuclear apoptosis, and a significant reduction in the concentration of macrophages in the connective tissue surrounding muscle fibers. However, muscle fiber invasion by macrophages was not reduced significantly in double mutant mice. Thus, cytotoxic T-lymphocytes contribute significantly to apoptosis and necrosis in mdx dystrophy, and perforin-mediated killing is primarily responsible for myonuclear apoptosis.
Full Text
The Full Text of this article is available as a PDF (360.0 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Arahata K., Engel A. G. Monoclonal antibody analysis of mononuclear cells in myopathies. I: Quantitation of subsets according to diagnosis and sites of accumulation and demonstration and counts of muscle fibers invaded by T cells. Ann Neurol. 1984 Aug;16(2):193–208. doi: 10.1002/ana.410160206. [DOI] [PubMed] [Google Scholar]
- Arahata K., Engel A. G. Monoclonal antibody analysis of mononuclear cells in myopathies. III: Immunoelectron microscopy aspects of cell-mediated muscle fiber injury. Ann Neurol. 1986 Feb;19(2):112–125. doi: 10.1002/ana.410190203. [DOI] [PubMed] [Google Scholar]
- Arahata K., Engel A. G. Monoclonal antibody analysis of mononuclear cells in myopathies. IV: Cell-mediated cytotoxicity and muscle fiber necrosis. Ann Neurol. 1988 Feb;23(2):168–173. doi: 10.1002/ana.410230210. [DOI] [PubMed] [Google Scholar]
- Berke G. The CTL's kiss of death. Cell. 1995 Apr 7;81(1):9–12. doi: 10.1016/0092-8674(95)90365-8. [DOI] [PubMed] [Google Scholar]
- Brooke M. H., Fenichel G. M., Griggs R. C., Mendell J. R., Moxley R. T., 3rd, Miller J. P., Kaiser K. K., Florence J. M., Pandya S., Signore L. Clinical investigation of Duchenne muscular dystrophy. Interesting results in a trial of prednisone. Arch Neurol. 1987 Aug;44(8):812–817. doi: 10.1001/archneur.1987.00520200016010. [DOI] [PubMed] [Google Scholar]
- Bulfield G., Siller W. G., Wight P. A., Moore K. J. X chromosome-linked muscular dystrophy (mdx) in the mouse. Proc Natl Acad Sci U S A. 1984 Feb;81(4):1189–1192. doi: 10.1073/pnas.81.4.1189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Drachman D. B., Toyka K. V., Myer E. Prednisone in Duchenne muscular dystrophy. Lancet. 1974 Dec 14;2(7894):1409–1412. doi: 10.1016/s0140-6736(74)90071-3. [DOI] [PubMed] [Google Scholar]
- Eichbaum Q. G., Beatty D. W., Parker M. I. Identification of cardiac autoantigens in human heart cDNA libraries using acute rheumatic fever sera. J Autoimmun. 1994 Apr;7(2):243–261. doi: 10.1006/jaut.1994.1019. [DOI] [PubMed] [Google Scholar]
- Emslie-Smith A. M., Arahata K., Engel A. G. Major histocompatibility complex class I antigen expression, immunolocalization of interferon subtypes, and T cell-mediated cytotoxicity in myopathies. Hum Pathol. 1989 Mar;20(3):224–231. doi: 10.1016/0046-8177(89)90128-7. [DOI] [PubMed] [Google Scholar]
- Engel A. G., Arahata K. Monoclonal antibody analysis of mononuclear cells in myopathies. II: Phenotypes of autoinvasive cells in polymyositis and inclusion body myositis. Ann Neurol. 1984 Aug;16(2):209–215. doi: 10.1002/ana.410160207. [DOI] [PubMed] [Google Scholar]
- Engel A. G., Arahata K. Mononuclear cells in myopathies: quantitation of functionally distinct subsets, recognition of antigen-specific cell-mediated cytotoxicity in some diseases, and implications for the pathogenesis of the different inflammatory myopathies. Hum Pathol. 1986 Jul;17(7):704–721. doi: 10.1016/s0046-8177(86)80180-0. [DOI] [PubMed] [Google Scholar]
- Fenichel G. M., Florence J. M., Pestronk A., Mendell J. R., Moxley R. T., 3rd, Griggs R. C., Brooke M. H., Miller J. P., Robison J., King W. Long-term benefit from prednisone therapy in Duchenne muscular dystrophy. Neurology. 1991 Dec;41(12):1874–1877. doi: 10.1212/wnl.41.12.1874. [DOI] [PubMed] [Google Scholar]
- Flanagan S. W., Ryan A. J., Gisolfi C. V., Moseley P. L. Tissue-specific HSP70 response in animals undergoing heat stress. Am J Physiol. 1995 Jan;268(1 Pt 2):R28–R32. doi: 10.1152/ajpregu.1995.268.1.R28. [DOI] [PubMed] [Google Scholar]
- Gavrieli Y., Sherman Y., Ben-Sasson S. A. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J Cell Biol. 1992 Nov;119(3):493–501. doi: 10.1083/jcb.119.3.493. [DOI] [PMC free article] [PubMed] [Google Scholar]
- González-Quintial R., Baccalá R., Pope R. M., Theofilopoulos A. N. Identification of clonally expanded T cells in rheumatoid arthritis using a sequence enrichment nuclease assay. J Clin Invest. 1996 Mar 1;97(5):1335–1343. doi: 10.1172/JCI118550. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Griggs R. C., Moxley R. T., 3rd, Mendell J. R., Fenichel G. M., Brooke M. H., Pestronk A., Miller J. P. Prednisone in Duchenne dystrophy. A randomized, controlled trial defining the time course and dose response. Clinical Investigation of Duchenne Dystrophy Group. Arch Neurol. 1991 Apr;48(4):383–388. doi: 10.1001/archneur.1991.00530160047012. [DOI] [PubMed] [Google Scholar]
- Gussoni E., Pavlath G. K., Miller R. G., Panzara M. A., Powell M., Blau H. M., Steinman L. Specific T cell receptor gene rearrangements at the site of muscle degeneration in Duchenne muscular dystrophy. J Immunol. 1994 Nov 15;153(10):4798–4805. [PubMed] [Google Scholar]
- Hoffman E. P., Brown R. H., Jr, Kunkel L. M. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell. 1987 Dec 24;51(6):919–928. doi: 10.1016/0092-8674(87)90579-4. [DOI] [PubMed] [Google Scholar]
- Jegadeesh Babu G., Prabhakar R., Kartha C. C., Rajamanickam C. Expression of proto-oncogenes, genes for muscle specific isoforms and heat shock protein (HSP) -70 gene in hypertrophied cardiac muscles from patients with atrial septal defect or tetralogy of Fallot. Biochem Mol Biol Int. 1994 Oct;34(3):627–637. [PubMed] [Google Scholar]
- Kennedy M. K., Picha K. S., Fanslow W. C., Grabstein K. H., Alderson M. R., Clifford K. N., Chin W. A., Mohler K. M. CD40/CD40 ligand interactions are required for T cell-dependent production of interleukin-12 by mouse macrophages. Eur J Immunol. 1996 Feb;26(2):370–378. doi: 10.1002/eji.1830260216. [DOI] [PubMed] [Google Scholar]
- Kissel J. T., Burrow K. L., Rammohan K. W., Mendell J. R. Mononuclear cell analysis of muscle biopsies in prednisone-treated and untreated Duchenne muscular dystrophy. CIDD Study Group. Neurology. 1991 May;41(5):667–672. doi: 10.1212/wnl.41.5.667. [DOI] [PubMed] [Google Scholar]
- Kunkel L. M., Hoffman E. P. Duchenne/Becker muscular dystrophy: a short overview of the gene, the protein, and current diagnostics. Br Med Bull. 1989 Jul;45(3):630–643. doi: 10.1093/oxfordjournals.bmb.a072349. [DOI] [PubMed] [Google Scholar]
- Kägi D., Ledermann B., Bürki K., Seiler P., Odermatt B., Olsen K. J., Podack E. R., Zinkernagel R. M., Hengartner H. Cytotoxicity mediated by T cells and natural killer cells is greatly impaired in perforin-deficient mice. Nature. 1994 May 5;369(6475):31–37. doi: 10.1038/369031a0. [DOI] [PubMed] [Google Scholar]
- Kägi D., Vignaux F., Ledermann B., Bürki K., Depraetere V., Nagata S., Hengartner H., Golstein P. Fas and perforin pathways as major mechanisms of T cell-mediated cytotoxicity. Science. 1994 Jul 22;265(5171):528–530. doi: 10.1126/science.7518614. [DOI] [PubMed] [Google Scholar]
- Latif N., Baker C. S., Dunn M. J., Rose M. L., Brady P., Yacoub M. H. Frequency and specificity of antiheart antibodies in patients with dilated cardiomyopathy detected using SDS-PAGE and western blotting. J Am Coll Cardiol. 1993 Nov 1;22(5):1378–1384. doi: 10.1016/0735-1097(93)90546-d. [DOI] [PubMed] [Google Scholar]
- Maisch B. Autoreactivity to the cardiac myocyte, connective tissue and the extracellular matrix in heart disease and postcardiac injury. Springer Semin Immunopathol. 1989;11(4):369–395. doi: 10.1007/BF00201877. [DOI] [PubMed] [Google Scholar]
- McArdle A., Jackson M. J. Heat shock protein 70 expression in skeletal muscle. Biochem Soc Trans. 1996 Aug;24(3):485S–485S. doi: 10.1042/bst024485s. [DOI] [PubMed] [Google Scholar]
- McDonald S. W., Halliday J. Cell-mediated immune response after vasectomy in rats. J Reprod Fertil. 1992 Nov;96(2):529–535. doi: 10.1530/jrf.0.0960529. [DOI] [PubMed] [Google Scholar]
- McDouall R. M., Dunn M. J., Dubowitz V. Nature of the mononuclear infiltrate and the mechanism of muscle damage in juvenile dermatomyositis and Duchenne muscular dystrophy. J Neurol Sci. 1990 Nov;99(2-3):199–217. doi: 10.1016/0022-510x(90)90156-h. [DOI] [PubMed] [Google Scholar]
- Mokri B., Engel A. G. Duchenne dystrophy: electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber. Neurology. 1975 Dec;25(12):1111–1120. doi: 10.1212/wnl.25.12.1111. [DOI] [PubMed] [Google Scholar]
- Morgan J. E., Partridge T. A. Cell transplantation and gene therapy in muscular dystrophy. Bioessays. 1992 Sep;14(9):641–645. doi: 10.1002/bies.950140913. [DOI] [PubMed] [Google Scholar]
- Mullis K., Faloona F., Scharf S., Saiki R., Horn G., Erlich H. Specific enzymatic amplification of DNA in vitro: the polymerase chain reaction. 1986. Biotechnology. 1992;24:17–27. [PubMed] [Google Scholar]
- Nagata S. Apoptosis regulated by a death factor and its receptor: Fas ligand and Fas. Philos Trans R Soc Lond B Biol Sci. 1994 Aug 30;345(1313):281–287. doi: 10.1098/rstb.1994.0107. [DOI] [PubMed] [Google Scholar]
- Neu N., Pummerer C., Rieker T., Berger P. T cells in cardiac myosin-induced myocarditis. Clin Immunol Immunopathol. 1993 Aug;68(2):107–110. doi: 10.1006/clin.1993.1104. [DOI] [PubMed] [Google Scholar]
- Nuovo G. J., Becker J., Simsir A., Margiotta M., Khalife G., Shevchuk M. HIV-1 nucleic acids localize to the spermatogonia and their progeny. A study by polymerase chain reaction in situ hybridization. Am J Pathol. 1994 Jun;144(6):1142–1148. [PMC free article] [PubMed] [Google Scholar]
- Partridge T. Animal models of muscular dystrophy--what can they teach us? Neuropathol Appl Neurobiol. 1991 Oct;17(5):353–363. doi: 10.1111/j.1365-2990.1991.tb00735.x. [DOI] [PubMed] [Google Scholar]
- Pasternak C., Wong S., Elson E. L. Mechanical function of dystrophin in muscle cells. J Cell Biol. 1995 Feb;128(3):355–361. doi: 10.1083/jcb.128.3.355. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Puntschart A., Vogt M., Widmer H. R., Hoppeler H., Billeter R. Hsp70 expression in human skeletal muscle after exercise. Acta Physiol Scand. 1996 Aug;157(4):411–417. doi: 10.1046/j.1365-201X.1996.512270000.x. [DOI] [PubMed] [Google Scholar]
- Spencer M. J., Croall D. E., Tidball J. G. Calpains are activated in necrotic fibers from mdx dystrophic mice. J Biol Chem. 1995 May 5;270(18):10909–10914. doi: 10.1074/jbc.270.18.10909. [DOI] [PubMed] [Google Scholar]
- Spencer M. J., Lu B., Tidball J. G. Calpain II expression is increased by changes in mechanical loading of muscle in vivo. J Cell Biochem. 1997 Jan;64(1):55–66. doi: 10.1002/(sici)1097-4644(199701)64:1<55::aid-jcb9>3.0.co;2-z. [DOI] [PubMed] [Google Scholar]
- Spencer M. J., Tidball J. G. Calpain translocation during muscle fiber necrosis and regeneration in dystrophin-deficient mice. Exp Cell Res. 1996 Aug 1;226(2):264–272. doi: 10.1006/excr.1996.0227. [DOI] [PubMed] [Google Scholar]
- Tidball J. G., Albrecht D. E., Lokensgard B. E., Spencer M. J. Apoptosis precedes necrosis of dystrophin-deficient muscle. J Cell Sci. 1995 Jun;108(Pt 6):2197–2204. doi: 10.1242/jcs.108.6.2197. [DOI] [PubMed] [Google Scholar]
- Tidball J. G., Spencer M. J. PDGF stimulation induces phosphorylation of talin and cytoskeletal reorganization in skeletal muscle. J Cell Biol. 1993 Nov;123(3):627–635. doi: 10.1083/jcb.123.3.627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Torres L. F., Duchen L. W. The mutant mdx: inherited myopathy in the mouse. Morphological studies of nerves, muscles and end-plates. Brain. 1987 Apr;110(Pt 2):269–299. doi: 10.1093/brain/110.2.269. [DOI] [PubMed] [Google Scholar]
- Turner P. R., Fong P. Y., Denetclaw W. F., Steinhardt R. A. Increased calcium influx in dystrophic muscle. J Cell Biol. 1991 Dec;115(6):1701–1712. doi: 10.1083/jcb.115.6.1701. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Utz U., McFarland H. F. The role of T cells in multiple sclerosis: implications for therapies targeting the T cell receptor. J Neuropathol Exp Neurol. 1994 Jul;53(4):351–358. doi: 10.1097/00005072-199407000-00005. [DOI] [PubMed] [Google Scholar]
- Walsh C. M., Matloubian M., Liu C. C., Ueda R., Kurahara C. G., Christensen J. L., Huang M. T., Young J. D., Ahmed R., Clark W. R. Immune function in mice lacking the perforin gene. Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):10854–10858. doi: 10.1073/pnas.91.23.10854. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Watt D. J., Morgan J. E., Partridge T. A. Long term survival of allografted muscle precursor cells following a limited period of treatment with cyclosporin A. Clin Exp Immunol. 1984 Feb;55(2):419–426. [PMC free article] [PubMed] [Google Scholar]
- Zychlinsky A., Zheng L. M., Liu C. C., Young J. D. Cytolytic lymphocytes induce both apoptosis and necrosis in target cells. J Immunol. 1991 Jan 1;146(1):393–400. [PubMed] [Google Scholar]