Initial Stages of Angiogenesis after Acute Experimental Local Venous Outflow Disturbances and Application of Cell Technologies

  • I. V. Maiborodin
  • V. V. Morozov
  • V. A. Matveeva
  • A. A. Anikeev
  • R. V. Maslov
  • G. A. Chastikin
  • N. F. Figurenko
Translated from Kletochnye Tekhnologii v Biologii i Meditsine (Cell Technologies in Biology and Medicine)

The initial stages of angiogenesis in rats after transcutaneous injection of autologous bone marrow multipotent mesenchymal stromal cells transfected with GFP gene and stained cell membranes in the projection of ligated femoral vein were studied by fluorescent light and confocal laser microscopy. Large clusters of brightly fluorescing elongated fibroblast-like cells were seen in the paravasal tissue and in the postoperative scar and signs of angiogenesis were noted as soon as in 4 days. The injected cells not only formed new vessels, but also integrated into vessels formed by host cells. Some injected cells were phagocytizied by macrophages and the latter started to fluoresce due to the presence of the membrane dye. These macrophages within the specified period appeared in the regional inguinal lymph nodes where they formed clusters in the lymphoid parenchyma of the cortical substance.

Key Words

multipotent mesenchymal stromal cells ligation of the vein angiogenesis 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Borodin YUi, Grigor’ev VN. Lymph Node in Circulatory Disturbances. Novosibirsk, 1986. Russian.Google Scholar
  2. 2.
    Maiborodin IV, Morozov VV, Novikova YaV, Matveyeva VA, Artemyeva LV, Matveyev AL, Khomeniuk SV, Marchukov SV. Morphological results of stromal stem cells of bone marrow origin into the thrombosed vein in experiment. Morfologiya. 2016;149(2):21-26. Russian.Google Scholar
  3. 3.
    Maiborodin IV, Morozov VV, Markevich YV, Matveeva VA, Artem’eva LV, Matveev AL, Chastikin GA, Seryapina YV. Acceleration of angiogenesis after paravasal injection of mesenchymal stem cells at the site of modeled venous thrombosis. Bull. Exp. Biol. Med. 2015;159(1):128-133.CrossRefPubMedGoogle Scholar
  4. 4.
    Maiborodin IV, Matveyeva VA, Maslov RV, Onopriyenko NV, Kuznetsova IV, Chastikin GA, Anikeyev AA. Some reactions of the regional lymph nodes of rats after implantation of multipotent stromal cells adsorbed on polyhydroxyalkanoate into a bone tissue defect. Morfologiya. 2012;142(4):54-61.Google Scholar
  5. 5.
    Campo JJ, Aponte JJ, Nhabomba AJ, Sacarlal J, Angulo-Barturen I, Jimenez-Diaz MB, Alonso PL, Dobano C. Feasibility of flow cytometry for measurements of Plasmodium falciparum parasite burden in studies in areas of malaria endemicity by use of bidimensional assessment of YOYO-1 and autofluorescence. J. Clin. Microbiol. 2011;49(3):968-974.CrossRefPubMedPubMedCentralGoogle Scholar
  6. 6.
    Li F, Yang M, Wang L, Williamson I, Tian F, Qin M, Shah PK, Sharifi BG. Autofluorescence contributes to false-positive intracellular Foxp3 staining in macrophages: a lesson learned from flow cytometry. J. Immunol. Methods. 2012;386(1-2):101-107.CrossRefPubMedPubMedCentralGoogle Scholar
  7. 7.
    Mendes-Jorge L, Ramos D, Luppo M, Llombart C, Alexandre-Pires G, Nacher V, Melgarejo V, Correia M, Navarro M, Carretero A, Tafuro S, Rodriguez-Baeza A, Esperança-Pina JA, Bosch F, Ruberte J. Scavenger function of resident autofluorescent perivascular macrophages and their contribution to the maintenance of the blood-retinal barrier. Invest. Ophthalmol. Vis. Sci. 2009;50(12):5997-6005.CrossRefPubMedGoogle Scholar
  8. 8.
    Mitchell AJ, Pradel LC, Chasson L, Van Rooijen N, Grau GE, Hunt NH, Chimini G. Technical advance: autofluorescence as a tool for myeloid cell analysis. J. Leukoc. Biol. 2010;88(3):597-603.CrossRefPubMedGoogle Scholar
  9. 9.
    Potter KA, Simon JS, Velagapudi B, Capadona JR. Reduction of autofluorescence at the microelectrode-cortical tissue interface improves antibody detection. J. Neurosci. Methods. 2012;203(1):96-105.CrossRefPubMedGoogle Scholar
  10. 10.
    Watson J. Suppressing autofluorescence of erythrocytes. Biotech. Histochem. 2011;86(3):207. doi:  10.3109/10520295.2011.568971.CrossRefPubMedGoogle Scholar
  11. 11.
    Wu X, Pan L, Wang Z, Liu X, Zhao D, Zhang X, Rupp RA, Xu J. Ultraviolet irradiation induces autofluorescence enhancement via production of reactive oxygen species and photodecomposition in erythrocytes. Biochem. Biophys. Res. Commun. 2010;396(4):999-1005.CrossRefPubMedGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2017

Authors and Affiliations

  • I. V. Maiborodin
    • 1
  • V. V. Morozov
    • 1
  • V. A. Matveeva
    • 1
  • A. A. Anikeev
    • 1
  • R. V. Maslov
    • 1
  • G. A. Chastikin
    • 1
  • N. F. Figurenko
    • 1
  1. 1.Center of New Medical Technologies, Institute of Chemical Biology and Fundamental MedicineSiberian Division of the Russian Academy of SciencesNovosibirskRussia

Personalised recommendations