Cyclic adenosine monophosphate levels and the function of skin microvascular endothelial cells

The maintenance of the normal epithelioid morphology of human dermal microvascular endothelial cells (MEC) grown in vitro depends strongly on the presence of factors that increase intracellular levels of cyclic AMP. Complete removal of dibutyryl cAMP and isobutylmethyixanthine (IMX) from the growth medium results in a progressive transition from an epithelioid to a spindle‐shaped cell line. This transition cannot be reversed by the readdition of dibutyryl cAMP and IMX to the growth medium or by addition of agonists that increase cAMP levels. Spindle‐shaped MEC lose the ability to express Factor VIII rAG and DR antigens and to bind peripheral blood mononuclear leukocyte (PBML).

[1]  R. Tuder,et al.  Adult cutaneous hemangiomas are composed of nonreplicating endothelial cells. , 1987, The Journal of investigative dermatology.

[2]  H. Hashimoto,et al.  Histogenesis of Kaposi's sarcoma associated with AIDS: a histologic, immunohistochemical and enzyme histochemical study. , 1987, Pathology, research and practice.

[3]  Michael Loran Dustin,et al.  Induction by IL 1 and interferon-gamma: tissue distribution, biochemistry, and function of a natural adherence molecule (ICAM-1). , 1986, Journal of immunology.

[4]  N. Minato,et al.  Mechanisms of lymphocyte adhesion to human vascular endothelial cells in culture. T lymphocyte adhesion to endothelial cells through endothelial HLA-DR antigens induced by gamma interferon. , 1986, The Journal of clinical investigation.

[5]  W. Fiers,et al.  Recombinant tumor necrosis factor and immune interferon act singly and in combination to reorganize human vascular endothelial cell monolayers. , 1986, The American journal of pathology.

[6]  F. Bonetti,et al.  The expression of endothelial cell surface antigens by AIDS-associated Kaposi's sarcoma. Evidence for a vascular endothelial cell origin. , 1986, The American journal of pathology.

[7]  P. Lipsky,et al.  Antigen presentation by interferon-gamma-treated endothelial cells and fibroblasts: differential ability to function as antigen-presenting cells despite comparable Ia expression. , 1985, Journal of immunology.

[8]  R. Auerbach,et al.  Expression of organ-specific antigens on capillary endothelial cells. , 1985, Microvascular research.

[9]  L. Orci,et al.  Human endothelial cell cultures: Phenotypic modulation by leukocyte interleukins , 1985, Journal of cellular physiology.

[10]  R. Dorfman Kaposi's sarcoma revisited. , 1984, Human pathology.

[11]  S. Shak,et al.  Prostaglandin I2 is not a major metabolite of arachidonic acid in cultured endothelial cells from human foreskin microvessels. , 1984, The Journal of clinical investigation.

[12]  W. Fiers,et al.  Ia expression by vascular endothelium is inducible by activated T cells and by human gamma interferon , 1983, The Journal of experimental medicine.

[13]  K. Bensch,et al.  Factors controlling the in vitro growth pattern of human microvascular endothelial cells. , 1983, Journal of Ultrastructure Research.

[14]  M. Mihm,et al.  T cell subsets in allograft rejection. In situ characterization of T cell subsets in human skin allografts by the use of monoclonal antibodies. , 1982, Journal of immunology.

[15]  L. Klareskog,et al.  In situ identification of T lymphocyte subsets and HLA-DR expressing cells in the human skin tuberculin reaction. , 1982, Clinical and experimental immunology.

[16]  D. Friedman Regulation of the Cell Cycle and Cellular Proliferation by Cyclic Nucleotides , 1982 .

[17]  M. Karasek,et al.  Human dermal microvascular endothelial cells in vitro: Effect of cyclic AMP on cellular morphology and proliferation rate , 1981, Journal of cellular physiology.

[18]  K. Bensch,et al.  Isolation and growth of endothelial cells from the microvessels of the newborn human foreskin in cell culture. , 1980, The Journal of investigative dermatology.

[19]  E. Thorsby,et al.  Stimulation of human lymphocytes by allogeneic endothelial cells in vitro. , 2008, Tissue antigens.