Skip to main content
Log in

Immunohistological and ultrastructural study of the developing tendons of the avian foot

  • Original Article
  • Published:
Anatomy and Embryology Aims and scope Submit manuscript

Abstract

The aim of the present report is to provide a detailed description of the morphogenesis and initial differentiation of the long tendons of the chick foot, the long autopodial tendons (LAT), from day 6 to day 11 of development. The fine structure of the developing LAT was studied by light and transmission electron microscopy. The characterization by immunofluorescent techniques of the extracellular matrix was performed using laser scanning confocal (tenascin, elastin, fibrillin, emilin, collagen type I, II, III, IV and VI) or routine fluorescence (tenascin, 13F4) microscopy. In addition, cell proliferation in pretendinous blastemas was analyzed by the detection of BrdU incorporation by immunofluorescence. The light microscopic analysis permitted the identification of different stages during LAT morphogenesis. The first stage is the formation of a thick ectoderm-mesenchyme interface along the digital rays, followed by the differentiation of the “mesenchyme lamina”, an extracellular matrix tendon precursor, and ending with the formation and differentiation of the cellular condensation that forms the tendon blastema around this lamina. The immunofluorescence study revealed the presence and arrangement of the different molecules analyzed. Tenascin and collagen type VI are precocious markers of the developing tendons and remain present during the whole process of tendon formation. Collagen type I becomes mainly restricted to the developing tendons from day 7.5. Collagens type II and IV are never detected in the developing tendons, while a faint labeling for collagen type III is first detected at day 7. The analysis of the distribution of the elastic matrix components in the developing tendons is a major contribution of our study. Elastin was detected in the periphery of the tendons from day 8 and also in fibrils anchoring the tendons to the skeletal elements. At the same stage, emilin strongly stains the core of the tendon rods, while fibrillin is detected a little later. Our study indicates the existence of an ectoderm-mesoderm interaction at the first stage of tendon formation. In addition, our results show the different spatial and temporal pattern of distribution of extracellular matrix molecules in developing tendons. Of special importance are the findings concerning the tendinous elastic matrix and its possible role in tendon maturation and stabilization.

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

  • Birk DE, Zycband E (1994) Assembly of the tendon extracellular matrix during development. J Anat 184:457–463

    Google Scholar 

  • Birk DE, Zycband EI, Winkelmann DA, Trelstad RL (1989) Collagen fibrillogenesis in situ: fibril segments are intermediates in matrix assembly. Proc Natl Acad Sci USA 86:4549–4553

    Google Scholar 

  • Brand B, Christ B, Jacob HJ (1985) An experimental analysis of the developmental capacities of the distal parts of avian leg buds. Am J Anat 173:321–340

    Google Scholar 

  • Bressan GM, Daga-Gordini D, Colombatti A, Castellani I, Marigo V, Volpin D (1993) Emilin, a component of elastic fibers preferentially located at the elastin-microfibrils interface. J Cell Biol 121:201–212

    Article  CAS  PubMed  Google Scholar 

  • Carvalho HE, Neto JL, Taboga SR (1994) Microfibrils: neglected components of pressure-bearing tendons. Ann Anat 176:155–159

    Google Scholar 

  • Chevallier A, Kieny M, Mauger A (1977) Limb-somite relationship: origin of the limb musculature. J Embryol Exp Morphol 41:245–258

    Google Scholar 

  • Chiquet M, Fambrough DM (1984) Chick myotendinous antigen. I. A monoclonal antibody as a marker for tendon and muscle morphogenesis. J Cell Biol 98:1926–1936

    Google Scholar 

  • Christ B, Jacob HJ, Jacob M (1974) Über den Ursprung der Flügelmuskulatur. Experimentelle Untersuchungen mit Wachtel- und Hühnerembryonen. Experientia 30:1446–1448

    CAS  PubMed  Google Scholar 

  • Christ B, Jacob HJ, Jacob M (1977) Experimental analysis of the origin of the wing musculature in avian embryos. Anat Embryol 150:171–186

    Google Scholar 

  • Critchlow M, Hinchliffe JR (1994) Immunolocalization of basement membrane components and β1 integrin in the chick wing bud identifies specialized properties of the apical ectodermal ridge. Dev Biol 163:253–269

    Google Scholar 

  • Curwin SL, Roy RR, Vailas AC (1994) Regional and age variations in growing tendon. J Morphol 221:309–320

    Google Scholar 

  • Dahlbäck K, Ljungquist A, Löfberg H, Dahlbäck B, Engvall E, Sakai LY (1990) Fibrillin immunoreactive fibers constitute a unique network in the human dermis: immunohistochemical comparison of the distributions of fibrillin, vitronectin, amyloid P component, and orcein stainable structures in normal skin and elastosis. I Invest Dermatol 94:284–291

    Google Scholar 

  • Davis EC (1994) Immunolocalization of microfibril and microfibril-associated proteins in the subendothelial matrix of the developing mouse aorta. J Cell Sci 107:727–736

    Google Scholar 

  • Dublet B, Van Der Rest M (1987) Type XII collagen is expressed in embryonic chick tendons. J Biol Chem 262:17724–17728

    Google Scholar 

  • Fitch JM, Gibney E, Sanderson RD, Mayne R, Linsenmayer TF (1982) Domain and basement membrane specificity of a monoclonal antibody against chicken type IV collagen. J Cell Biol 95:461–467

    Google Scholar 

  • Fleischmajer R, Perlish JS, Timpl R, Olsen BR (1988) Procollagen intermediates during tendon fibrillogenesis. J Histochem Cytochem 36:1425–1432

    Google Scholar 

  • Fleischmajer R, Perlish JS, Faraggiana T (1991) Rotary shadowing of collagen monomers, oligomers, and fibrils during tendon fibrillogenesis. J Histochem Cytochem 39:51–58

    Google Scholar 

  • Greenlee TK Jr, Ross R (1967) The development of the rat flexor digital tendon, a fine structure study. J Ultrastruct Res 18:354–362

    Google Scholar 

  • Hamburger V, Hamilton HL (1951) A series of normal stages in the development of the chick embryo. J Morphol 88:49–92

    Google Scholar 

  • Hay E (1991) Collagen and other matrix glycoproteins in embryogenesis. In: Hay ED (ed) Cell biology of the extracellular matrix, 2nd edn. Plenum Press, New York, pp 419–462

    Google Scholar 

  • Harris AJ, Fitzsimons RB, McEwan JC (1989) Neural control of the sequence of myosin heavy chain isoforms in foetal mammalian muscles. Development 107:751–769

    Google Scholar 

  • Holder N (1989) Organization of connective tissue patterns by dermal fibroblasts in the regenerating axolotl limb. Development 105:585–593

    Google Scholar 

  • Hurle JM, Hinchliffe JR, Ros MA, Critchlow MA, Genis-Galvez JM (1989) The extracellular matrix architecture relating to myotendinous pattern formation in the distal part of the developing chick limb: an ultrastructural, histochemical and immunocytochemical analysis. Cell Differ Dev 27:103–120

    Google Scholar 

  • Hurle JM, Ros MA, Gañan Y, Macias D, Critchlow M, Hinchliffe JR (1990) Experimental analysis of the role of ECM in the patterning of the distal tendons of the developing limb bud. Cell Differ 30:97–108

    Google Scholar 

  • Hurle JM, Corson G, Daniels K, Reiter R, Sakai LY, Solursh M (1994) Elastin exhibits a distinctive temporal and spatial pattern of distribution in the developing chick limb in association with the establishment of the cartilaginous skeleton. J Cell Sci 107:2623–2324

    Google Scholar 

  • Keeley FW, Alatawi A (1991) Response of aortic elastin synthesis and accumulation to developing hypertension and the inhibitory effect of colchicine on this response. Lab Invest 64:499–507.

    Google Scholar 

  • Kielty CM, Cummings C, Whittaker SP, Shuttleworth CA, Grant ME (1991) Isolation and ultrastructural analsyis of microfibrillar struuctures from foetal bovine elastic tissues. Relative abundance and supramolecular architecture of type VI collagen assemblies and fibrillin. J Cell Sci 99:797–807

    Google Scholar 

  • Kieny M, Chevallier A (1979) Autonomy of tendon development in the embryonic chick wing. J Embryol Exp Morphol 49:153–165

    Google Scholar 

  • Kieny M, Mauger A (1984) Immunofluorescent localization of extracellular matrix components during muscle morphogenesis. I. In normal chick embryos. J Exp Zool 232:327–341

    Google Scholar 

  • Kosher RA, Solursh M (1989) Widespread distribution of type II collagen during embryonic chick development. Dev Biol 131:558–566

    Google Scholar 

  • Linsenmayer TF, Hendrix MJC, Little CD (1979) Production and characterization of a monoclonal antibody to chicken type I collagen. Proc Nat Acad Sci USA 76:3703–3707

    Google Scholar 

  • Mallein-Gérin F (1990) Subepithelial type II collagen deposition during embryonic limb development. Rouxs Arch Dev Biol 198:363–369

    Google Scholar 

  • Mallein-Gŕin F, Garrone R (1990) Tendon collagen fibrillogenesis is a multistep assembly process as revealed by quick-freezing and freeze-substitution. Biol Cell 69:9–16

    Google Scholar 

  • Mecham RP, Heuser JE (1991) The elastic fiber. In: Hay ED (ed) Cell biology of the extracellular matrix, 2nd edn. Plenum Press, New York, pp 79–109

    Google Scholar 

  • Oliver G, Wehr R, Jenkins NA, Copeland NG, Cheyette BNR, Hartenstein V, Zipursky SL, Grass P (1995) Homeobox gene and connective tissue patterning. Development 121:693–705

    CAS  PubMed  Google Scholar 

  • Pasquali-Ronchetti I, Baccarini-Conti M, Fornieri C, Mori G, Quaglino D Jr (1993) Structure and composition of the elastic fiber in normal and pathological conditions. Micron 24:75–89

    Google Scholar 

  • Pautou MP, Hedayat I, Kieny M (1982) The pattern of muscle development in the chick leg. Arch Anat Microsc Morphol Exp 71:193–206

    Google Scholar 

  • Rong P-M, Ziller C, Pena-Melian A, Le Douarin NM (1987) A monoclonal antibody specific for avian early myogenic cells and differentiated muscle. Dev Biol 122:338–353

    Google Scholar 

  • Ros MA, Hinchliffe JR, Macias D, Hurle JM, Critchlow M (1991) Extracellular material organization and long tendon formation in the chick leg autopodium. In vivo and in vitro study. In: Hinchliffe JR, Hurle JM, Summerbell D (eds) Developmental patterning of the vertebrate limb. Plenum Press, New York, pp 211–214

    Google Scholar 

  • Rosenbloom J, Abrams WR, Mecham R (1993) Extracellular matrix. 4. The elastic fiber. FASEB J 7:1208–1218

    Google Scholar 

  • Ross R, Bornstein P (1969) The elastic fiber. I. The separation and partial characterization of its macromolecular components. J Cell Biol 40:366–381

    Google Scholar 

  • Sakai LY, Keene D, Engvall E (1986) Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils. J Cell Biol 103:2499–2509

    Google Scholar 

  • Scott JE (1984) The periphery of the developing collagen fibril. Quantitative relationships with dermatan sulphate and other surface-associated species. Biochem J 218:229–233

    Google Scholar 

  • Shellswell GB, Wolpert L (1977) The pattern of muscle and tendon development in the chick wing. In: Ede DA, Hinchliffe JR, Balls M (eds) Vertebrate limb and somite morphogenesis. Cambridge University Press, Cambridge, pp 71–86

    Google Scholar 

  • Shellswell GB, Bailey AJ, Duance VC, Restall DJ (1980) Has collagen a role in muscle pattern formation in the developing chick wing? I. An immunofluorescence study. J Embryol Exp Morph 60:245–254

    Google Scholar 

  • Singley CT, Solursh M (1980) The use of tannic acid for ultrastructural visualization of hyaluronic acid. Histochemistry 65:93–102

    Google Scholar 

  • Slack C, Flint MH, Thompson BM (1984) The effect of tensional load on isolated embryonic chick tendons in organ culture Connect Tissue Res 12:229–247

    Google Scholar 

  • Sullivan GE (1962) Anatomy and embryology of the wing musculature of the domestic fowl (Gallus). Aust J Zool 10:458–516

    Google Scholar 

  • Sutcliffe MC, Davidson JM (1990) Effect of static stretching on elastin production by porcine aortic smooth muscle cells. Matrix 10:148–153

    Google Scholar 

  • Swasdison S, Mayne R (1989) Location of the integrin complex and extracellular matrix molecules at the chicken myotendinous junction. Cell Tissue Res 257:537–543

    Google Scholar 

  • Tidball JG (1994) Assembly of myotendinous junctions in the chick embryo: deposition of P68 is an early event in myotendinous junction formation. Dev Biol 163:447–456

    Google Scholar 

  • Tsuzaki M, Yamauchi M, Banes AJ (1993) Tendon collagens: extracellular matrix composition in shear stress and tensile components of flexor tendons. Connet Tissue Res 29:141–152

    Google Scholar 

  • Vogel KG, Sandy JD, Pogany G, Robbins JR (1994) Aggrecan in bovine tendon. Matrix 14:171–179

    Google Scholar 

  • Watson SJ, Bekoff A (1990) A kinematic analysis of hindlimb motility in 9- and 10-day-old chick embryos. J Neurobiol 21:651–660

    Google Scholar 

  • Wortham RA (1948) The development of the muscles and tendons in the lower leg and foot of chick embryos. J Morphol 83:105–148

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ros, M.A., Rivero, F.B., Hinchliffe, J.R. et al. Immunohistological and ultrastructural study of the developing tendons of the avian foot. Anat Embryol 192, 483–496 (1995). https://doi.org/10.1007/BF00187179

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00187179

Key words

Navigation