Skip to main content
Log in

Arrangement of cytoskeletal filaments at the equator of chicken intrafusal muscle fibers

  • Published:
Histochemistry Aims and scope Submit manuscript

Summary

The organization of the cytoskeleton at the equator of chicken intrafusal fibers was examined with immunofluorescence light microscopy, using monoclonal antibodies against myosin heavy chains, desmin, actin and tropomyosin. Actin was localized in the cytosol and in equatorial nuclei, while myosin heavy chains, desmin and tropomyosin were only observed in the cytosol. Although all four proteins were present at the equator and at the pole, the fluorescence produced after incubation with the different antibodies varied considerably between the two regions. Staining at the pole was in the form of striations, but at the equator it was non-striated and more uniform. The observed fluorescent patterns suggest that at the equator filaments are assembled into looser arrays than in the sarcomeres of the pole. A flexible cytoskeleton at the equator would be an appropriate substrate for distorting the affixed sensory endings during an applied stress.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Adal M (1973) The fine structure of the intrafusal muscle fibres of muscle spindles in the domestic fowl. J Anat 115:407–413

    Google Scholar 

  • Armbruster BL, Wunderli H, Turner BM, Raska I, Kellenberger E (1983) Immunocytochemical localization of cytoskeletal proteins and histones 2B in isolated membrane-depleted nuclei, metaphase chromatin, and whole Chinese hamster ovary cells. J Histochem Cytochem 31:1385–1393

    Google Scholar 

  • Boyd IA (1962) The structure and innervation of the nuclear bag muscle fibre system and the nuclear chain muscle fibre system in mammalian muscle spindles. Phil Trans R Soc London B245:81–136

    Google Scholar 

  • Boyd IA (1976) The response of fast and slow nuclear bag fibres and nuclear chain fibres in isolated cat muscle spindles to fusimotor stimulation, and the effect of intrafusal contraction on the sensory endings. Q J Exp Physiol 61:203–254

    Google Scholar 

  • Boyd IA, Smith RS (1984) The muscle spindle. In: Dyck PJ, Thomas PK, Lombert EH, Bunge R (eds) Peripheral neuropathy, 2nd edn. WB Saunders, Philadelphia, pp 171–202

    Google Scholar 

  • Burridge K (1986) Substrate adhesions in normal and transformed fibroblasts: Organization and regulation of cytoskeletal, membrane and extracellular matrix components at focal contacts. Cancer Rev 4:18–78

    Google Scholar 

  • Crowley KS, Brasch K (1987) Does the interchromatin compartment contain actin? Cell Biol Int Rep 11:537–546

    Google Scholar 

  • Cooper S, Gladden MH (1974) Elastic fibres and reticulin of mammalian muscle spindles and their functional significance. Q J Exp Physiol 59:367–385

    Google Scholar 

  • Eldred E (1967) Peripheral receptors: Their excitation and relation to reflex patterns. Am J Phys Med 46:69–87

    Google Scholar 

  • Fay FS, Fogarty K (1984) The organization of the contractile apparatus in single isolated smooth muscle cells. In: Stephens NL (ed) Smooth muscle contraction. Marcel Dekker, New York, pp 75–90

    Google Scholar 

  • Fischman DA, Danto SI (1985) Monoclonal antibodies to desmin: Evidence for stage-dependent intermediate filament immunoreactivity during cardiac and skeletal muscle development. Ann NY Acad Sci 455:167–184

    Google Scholar 

  • Hikida RS (1985) Spaced serial section analysis of the avian muscle spindle. Anat Rec 212:255–267

    Google Scholar 

  • James NT, Meek GA (1973) An electron microscopical study of avian muscle spindles. J Ultrastruct Res 43:193–204

    Google Scholar 

  • Karnovsky MJ (1965) A formaldehyde-glutaraldehyde fixative of high osmolality for use in electron microscopy. J Cell Biol 27:137A-138A

    Google Scholar 

  • Kennedy JM, Kamel S, Tambone WW, Vrbova G, Zak R (1986) The expression of myosin heavy chain isoforms in normal and hypertrophied chicken slow muscle. J Cell Biol 103:977–983

    Google Scholar 

  • Lin JJC (1981) Monoclonal antibodies against myofibrillar components of rat skeletal muscle decorate the intermediate filaments of cultured cells. Proc Natl Acad Sci USA 78:2335–2339

    Google Scholar 

  • Lin JJC, Chou CS, Lin JLC (1985) Monoclonal antibodies against chicken tropomyosin isoforms: production, characterization, and application. Hybridoma 4:223–242

    Google Scholar 

  • Maier A (1977) Variations in intrafusal fiber size within histochemically identified types of intrafusal fiber in the pigeon. Am J Anat 150:375–380

    Google Scholar 

  • Maier A (1981) Characteristics of pigeon gastrocnemius and its muscle spindle supply. Exp Neurol 74:892–906

    Google Scholar 

  • Maier A (1985) Ultrastructure of the equatorial region of chick forearm muscle spindles. Anat Rec 211:121A

    Google Scholar 

  • Maier A (1989) Contours and distribution of sites that react with antiacetylcholinesterase in chicken intrafusal fibers. Am J Anat 185:33–44

    Google Scholar 

  • Maier A, Eldred E (1971) Comparisons in the structure of avian muscle spindles. J Comp Neurol 143:25–40

    Google Scholar 

  • Maier A, Mayne R (1987) Distribution of connective tissue proteins in chick muscle spindles as revealed by monoclonal antibodies: A unique distribution of brachionectin/tenascin. Am J Anat 180:226–236

    Google Scholar 

  • Milburn A (1973) The early development of muscle spindles in the rat. J Cell Sci 12:175–195

    Google Scholar 

  • Milburn A (1984) Stages in the development of cat muscle spindles. J Embryol Exp Morphol 82:177–216

    Google Scholar 

  • Otey CA, Kalnoski MH, Bulinski JC (1988) Immunolocalization of muscle and non-muscle isoforms of actin in myogenic cells and adult skeletal muscle. Cell Motil Cytoskel 9:337–348

    Google Scholar 

  • Ovalle WK (1978) Histochemical dichotomy of extrafusal and intrafusal fibers in avian slow muscle. Am J Anat 152:587–597

    Google Scholar 

  • Ovalle WK (1989) Ultrastructural morphometry of amphibian and avian intrafusal muscle fibers. Anat Rec 223:86A

    Google Scholar 

  • Rebollo MA, DeAnda G (1967) Morphology of neuromuscular spindles in the chicken during development. Acta Neurol Latinoam. 13:150–155

    Google Scholar 

  • Saglam M (1968) Morphologische und quantitative Untersuchungen über die Muskelspindeln in der Nackenmuskulatur (M. biventer cervicis, M. rectus capitis dorsalis und M. rectus capitis lateralis) des Bunt- and Blutspechtes. Acta Anat 69:87–104

    Google Scholar 

  • Somlyo AV, Bond M, Butler TM, Berner DF, Ashton FT, Holtzer H, Somlyo AP (1984) The contractile apparatus of smooth muscle: an update. In: Stephens NL (ed) Smooth muscle contraction. Marcel Dekker, New York, pp 1–20

    Google Scholar 

  • Sweeney LJ, Zak R, Manasek FJ (1987) Transitions in cardiac isomyosins expression during differentiation of the embryonic chick heart. Circ Res 61:287–295

    Google Scholar 

  • Wang K (1983) Membrane skeleton of skeletal muscle. Nature 304:485–486

    Google Scholar 

  • Wehland J, Weber K (1980) Distribution of fluorescently labeled actin and tropomyosin after microinjection in living tissue culture cells as observed with TV image intensification. Exp Cell Res 127:397–408

    Google Scholar 

  • Zelena J (1957) The morphogenetic influence of innervation on the ontogenetic development of muscle spindles. J Embryol Exp Morphol 5:283–292

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Maier, A., Zak, R. Arrangement of cytoskeletal filaments at the equator of chicken intrafusal muscle fibers. Histochemistry 93, 423–428 (1990). https://doi.org/10.1007/BF00315861

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00315861

Keywords

Navigation