Skip to main content
Log in

Stability of elastin in the developing mouse aorta: a quantitative radioautographic study

  • Originals
  • Published:
Histochemistry Aims and scope Submit manuscript

Abstract

Elastic lamina growth during development and the ultimate stability of elastin in the mouse aortic media was investigated by light and electron microscopic radioautography. Following a single subcutaneous injection of l-[3,4-3H]valine at 3 days of age, animals were killed at 9 subsequent time intervals up to 4 months of age. One day after injection, radioautographic silver grains were primarily observed over the elastic laminae; however, silver grains were also seen over the smooth muscle cells and extracellular matrix. By 21 to 28 days of age, the silver grains were almost exclusively located over the elastic laminae. From 28 days to 4 months of age, the distribution of silver grains appeared relatively unchanged. Quantitation of silver grain number/μm2 of elastin showed a steady decrease in the concentration of silver grains associated with the elastic laminae from 4 to 21 days of age. After this time, no significant difference in silver grain concentration was observed. Since the initial decrease in grains/μm2 of elastin corresponds to a period of rapid post-natal growth, the decrease is likely to be a result of dilution of the radiolabel due to new elastin synthesis. With the assumption that little or no significant turnover occurs during this time, a constant growth rate of 4.3% per day was predicted by linear regression analysis. Since no significant difference in the concentration of silver grains was observed from 28 to 118 days of age, no new growth or turnover of elastin can be said to occur during this time period. This is supported by the observation that animals injected with radiolabeled valine at 28 days and 8 months of age showed no significant incorporation of radiolabel into the elastic laminae. The results from this study present the first long-term radioautographic evidence of the stability of aortic elastin and emphasize that initial deposition of elastin and proper assembly of elastic laminae is a critical event in vessel development.

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.

Institutional subscriptions

Similar content being viewed by others

References

  • Bendeck MP, Langille BL (1991) Rapid accumulation of elastin and collagen in the aortas of sheep in the immediate perinatal period. Circ Res 69:1165–1169

    Google Scholar 

  • Berry CL, Looker T, Germain J (1972) Nucleic acid and scleroprotein content of the developing human aorta. J Pathol 108:265–274

    Google Scholar 

  • Daga-Gordini D, Bressan GM, Castellani I, Volpin D (1987) Fine mapping of tropoelastin-derived components in the aorta of developing chick embryo. Histochem J 19:623–632

    Google Scholar 

  • Davidson JM, Hill KE, Alford JL (1986) Developmental changes in collagen and elastin biosynthesis in the porcine aorta. Dev Biol 118:103–111

    Google Scholar 

  • Davis EC (1993) Smooth muscle cell to elastic lamina connections in the developing mouse aorta: Role in aortic medial organization. Lab Invest 68:89–99

    Google Scholar 

  • Dubick MA, Rucker RB, Cross CE, Last JA (1981) Elastin metabolism in the rodent lung. Biochim Biophys Acta 672:303–306

    Google Scholar 

  • Fahrenbach WH, Sandberg LB, Clearly EG (1966) Ultrastructural studies on early elastogenesis. Anat Rec 155:563–576

    Google Scholar 

  • Fischer GM (1971) Dynamics of collagen and elastin metabolism in rat aorta. J Appl Physiol 31:527–530

    Google Scholar 

  • Fischer GM, Swain ML (1978) In vivo effects of sex hormones on aortic elastin and collagen dynamics in castrated and intact male rats. Endocrinology 102:92–97

    Google Scholar 

  • Franc S, Garrone R, Bosch A, Franc J-M (1984) A routine method for contrasting elastin at the ultrastructural level. J Histochem Cytochem 32:251–258

    Google Scholar 

  • Gerrity RG, Cliff WJ (1975) The aortic tunica media of the developing rat. I. Quantitative stereologic and biochemical analysis. Lab Invest 32:585–600

    Google Scholar 

  • Gerrity RG, Adams EP, Cliff WJ (1975) The aortic tunica media of the developing rat. II. Incorporation by medial cells of 3H-proline into collagen and elastin: autoradiographic and chemical studies. Lab Invest 32:601–609

    Google Scholar 

  • Kao K-YT, Hilker DM, McGavack TH (1961) Connective tissue. V. Comparison of synthesis and turnover of collagen and elastin in tissues of rat at several ages. Proc Soc Exp Biol Med 106:335–338

    Google Scholar 

  • Keeley FW (1979) The synthesis of soluble and insoluble elastin in chicken aorta as a function of development and age. Effect of a high cholesterol diet. Can J Biochem 57:1273–1280

    Google Scholar 

  • Keeley FW, Johnson DJ (1983) Measurement of the absolute synthesis of soluble and insoluble elastin by chick aortic tissue. Can J Biochem Cell Biol 61:1079–1084

    Google Scholar 

  • Kopriwa BM (1973) A reliable, standardized method for ultrastructural electron microscopic radioautography. Histochemie 37:1–17

    Google Scholar 

  • Kopriwa BM, Leblond CP (1962) Improvements in the coating technique of radioautography. J Histochem Cytochem 10:269–284

    Google Scholar 

  • Lee I, Yau MC, Rucker RB (1976) Arterial elastin synthesis in the young chick. Biochim Biophys Acta 442:432–436

    Google Scholar 

  • Lefevre M, Rucker RB (1980) Aorta elastin turnover in normal and hypercholesterolemic Japanese quail. Biochim Biophys Acta 630:519–529

    Google Scholar 

  • Looker T, Berry CL (1972) The growth and development of the rat aorta. II. Changes in nucleic acid and scleroprotein content. J Anat 113:17–34

    Google Scholar 

  • Nakamura H (1988) Electron microscopic study of the prenatal development of the thoracic aorta in the rat. Am J Anat 181:406–418

    Google Scholar 

  • Reynolds ES (1963) The use of lead citrate at high pH as an electron opaque stain in electron microscopy. J Cell Biol 17:208–215

    Google Scholar 

  • Ross R, Klebanoff SJ (1971) The smooth muscle cell. I. In vivo synthesis of connective tissue proteins. J Cell Biol 50:159–171

    Google Scholar 

  • Rucker RB, Tinker D (1977) Structure and metabolism of arterial elastin. Int Rev Exp Pathol 17:1–47

    Google Scholar 

  • Shapiro SD, Endicott SK, Province MA, Pierce JA, Campbell EJ (1991) Marked longevity of human lung parenchymal elastic fibers deduced from prevalence of d-aspartate and nuclear weapons-related radiocarbon. J Clin Invest 87:1828–1834

    Google Scholar 

  • Slack HGB (1954) Metabolism of elastin in the adult rat. Nature 174:512–513

    Google Scholar 

  • Walford RL, Carter PK, Schneider RB (1964) Stability of aortic elastic tissue with age and pregnancy in the rat. Arch Pathol 78:43–45

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Davis, E.C. Stability of elastin in the developing mouse aorta: a quantitative radioautographic study. Histochemistry 100, 17–26 (1993). https://doi.org/10.1007/BF00268874

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00268874

Keywords

Navigation