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Angiogenesis and the formation of lymphaticlike channels in cultures of thoracic duct

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Summary

Segments of rat thoracic duct cultured in plasma clot or in collagen gel produced microvascular and fibroblastic outgrowths. Lymphaticlike channels (LLC) with a highly attenuated endothelium, which was barely visible by light microscopy, were found in 8 out of 25 cultures (32%). Serial histologic sections revealed that the endothelium of the LLC was continuous with the intimal endothelium of the throacic duct and was therefore of lymphatic origin. In addition to the LLC, vascular channels lined by a thick endothelium with hump-shaped, cross-sectional profiles were found in 10 cultures (40%). These channels were indistinguishable from the microvessels of blood vascular origin that formed in parallel cultures of rat aorta or periductal adipose tissue and were termed hematiclike channels (HLC). Contrary to the LLC, the HLC did not originate from the lymphatic endothelium of the thoracic duct. The frequent association of the HLC with the adventitia of the thoracic duct and with the surrounding adipose tissue suggested that they probably developed from the hematic microvessels of the periductal soft tissues.

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References

  1. Casley-Smith, J. R. Lymph and lymphatics. In: Kaley, G.; Altura, B. M., eds. Microcirculation, vol. 1. Baltimore, MD: University Park Press; 1977: 423–502.

    Google Scholar 

  2. Clark, E. R.; Clark, E. L. Observations on the new growth of lymphatic vessels as seen in transparent chambers introduced into the rabbit’s ear. Am. J. Anat. 51(1):43–87; 1932.

    Article  Google Scholar 

  3. Huntington, G. S. The development of the mammalian jugular lymph sac, of the tributary primitive ulnar lymphatic, and of the thoracic duct. Am. J. Anat. 16:259–316; 1914.

    Article  Google Scholar 

  4. Jaffe, E. A. Physiologic functions of normal endothelial cells. In: Lee, K. T., ed. Atherosclerosis. Ann. NY Acad. Sci, vol. 454. New York: New York Academy of Science; 1985; 279–291.

    Google Scholar 

  5. Johnston, M. G.; Walker, M. A. Lymphatic endothelial and smooth muscle cells in tissue culture. In Vitro 20(7):566–572; 1984.

    PubMed  CAS  Google Scholar 

  6. Leak, L. V. Electron microscopic observations on lymphatic capillaries and the structural components of the connective tissue-lymph interface. Microvasc. Res. 2:361–391; 1970.

    Article  PubMed  CAS  Google Scholar 

  7. Leak, L. V.; Burke, J. F. Ultrastructural studies on the lymphatic anchoring filaments. J. Cell Biol. 36:129–149; 1968.

    Article  Google Scholar 

  8. Leak, L. V.; Burke, J. F. Early events of tissue injury and the role of the lymphatic system in early inflammation. In: Zweifach, B. W.; Grant, L.; McCloskey, R. T., eds. The inflammatory process, vol. 3. New York: Academic Press; 1974: 163–236.

    Google Scholar 

  9. Maciag, T. Angiogenesis. Prog. Hemost. Thromb. 7:167–182; 1984.

    PubMed  CAS  Google Scholar 

  10. Montesano, R.; Orci, L.; Vassalli, P. In Vitro rapid organization of endothelial cells into capillary-like networks is promoted by collagen matrices. J. Cell Biol. 97:1648–1652; 1983.

    Article  PubMed  CAS  Google Scholar 

  11. Nicosia, R. F.; Tchao, R.; Leighton, J. Histotypic angiogenesis in vitro: light microscopic, ultrastructural, and radioautographic studies. In Vitro 18:538–549; 1982.

    PubMed  CAS  Google Scholar 

  12. Reynolds, E. S. The use of lead citrate at high pH as an electronopaque stain in electron microscopy. J. Cell Biol. 17:208–212; 1963.

    Article  PubMed  CAS  Google Scholar 

  13. Sabin, F. R. On the origin and development of the lymphatic system from the veins and the development of the lymph hearts and the thoracic duct in the pig. Am. J. Anat. 1:367–389; 1902.

    Article  Google Scholar 

  14. Sandison, J. C. Observation on growth of blood vessels as seen in transparent chamber introduced into rabbits’s ear. Am. J. Anat. 41:475–496; 1928.

    Article  Google Scholar 

  15. Schoefl, G. I. Studies on inflammation III. Growing capillaries: their structure and permeability. Virchows Arch. [A] 337:97–141; 1963.

    CAS  Google Scholar 

  16. Willis, R. A. Metastasis via lymphatics and the cancerous thoracic duct. The spread of tumours in the human body. St. Louis: C. V. Mosby Co.; 1952: 18–35.

    Google Scholar 

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This research was supported by grants from the National Cancer Institute, NIH, National Bladder Cancer Project (CA14137), and the W. W. Smith Charitable Trust.

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Nicosia, R.F. Angiogenesis and the formation of lymphaticlike channels in cultures of thoracic duct. In Vitro Cell Dev Biol 23, 167–174 (1987). https://doi.org/10.1007/BF02623576

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