Macrophage production of basic fibroblast growth factor in the fibroproliferative disorder of alveolar fibrosis after lung injury.

In organ repair following injury, macrophages accumulate and granulation tissue, comprised of fibroblasts and endothelial cells, develops in the injured area. Basic fibroblast growth factor (bFGF), a potent stimulator of fibroblast and endothelial cell growth, has been linked to the fibroproliferative process. Macrophages are thought to play a central role in the fibroproliferative response, and prior studies indicate that they produce bFGF. Whereas it is plausible that macrophages produce bFGF in a fibroproliferative process, currently no data exists that directly identifies the macrophage as a source of bFGF in a fibroproliferative disorder. We used the model of acute intraalveolar granulation tissue formation following lung injury to determine if the macrophage was a cellular source of bFGF in a naturally occurring fibroproliferative process. To examine this hypothesis, patients with severe acute lung injury underwent bronchoalveolar lavage during the phase of lung repair. Polymerase chain reaction and Northern analysis of macrophage RNA revealed the presence of two species of bFGF messenger RNA (4.4 kb and 1.9 kb). Metabolic labeling studies of recovered macrophages revealed a newly synthesized 18-kd protein with antigenic similarity to bFGF. Immunohistochemical evaluation of lung tissue from patients who died following acute lung injury, showed numerous bFGF immunoreactive macrophages present within airspaces containing fibroblastic and vascular tissue proliferation. This investigation has identified the alveolar macrophage as a cellular source of bFGF in the fibroproliferative disorder of intraalveolar fibrosis following acute lung injury.

[1]  A. Isacchi,et al.  Basic fibroblast growth factor in Dupuytren's contracture. , 1992, The American journal of pathology.

[2]  M. Peterson,et al.  Identification and partial characterization of angiogenesis bioactivity in the lower respiratory tract after acute lung injury. , 1991, The Journal of clinical investigation.

[3]  D. Hanahan,et al.  Neovascularization is associated with a switch to the export of bFGF in the multistep development of fibrosarcoma , 1991, Cell.

[4]  M. Ferguson,et al.  Immunohistochemical localization of growth factors in fetal wound healing. , 1991, Developmental biology.

[5]  M. Peterson,et al.  Acute lung injury. Pathogenesis of intraalveolar fibrosis. , 1991, The Journal of clinical investigation.

[6]  P. Mcneil,et al.  Basic fibroblast growth factor is efficiently released from a cytolsolic storage site through plasma membrane disruptions of endothelial cells , 1991, Journal of cellular physiology.

[7]  E. Vollmer,et al.  In situ detection of basic fibroblast growth factor by highly specific antibodies. , 1990, The American journal of pathology.

[8]  D. Rifkin,et al.  Monospecific antibodies implicate basic fibroblast growth factor in normal wound repair. , 1989, Laboratory investigation; a journal of technical methods and pathology.

[9]  D. Knighton,et al.  Macrophage-derived growth factors in wound healing: regulation of growth factor production by the oxygen microenvironment. , 1989, The American review of respiratory disease.

[10]  D. Rifkin,et al.  Recent developments in the cell biology of basic fibroblast growth factor , 1989, The Journal of cell biology.

[11]  M J Banda,et al.  Wound macrophages express TGF-alpha and other growth factors in vivo: analysis by mRNA phenotyping. , 1988, Science.

[12]  A. Sommer,et al.  Recombinant basic fibroblast growth factor accelerates wound healing. , 1988, The Journal of surgical research.

[13]  D. Ingber,et al.  A heparin-binding angiogenic protein--basic fibroblast growth factor--is stored within basement membrane. , 1988, The American journal of pathology.

[14]  R. G. Clerc,et al.  Two calcium-binding proteins in infiltrate macrophages of rheumatoid arthritis , 1987, Nature.

[15]  R. Centor,et al.  The adult respiratory distress syndrome. Cell populations and soluble mediators in the air spaces of patients at high risk. , 1987, The American review of respiratory disease.

[16]  P. Matsudaira,et al.  Sequence from picomole quantities of proteins electroblotted onto polyvinylidene difluoride membranes. , 1987, The Journal of biological chemistry.

[17]  J. Folkman,et al.  Endothelial cell-derived basic fibroblast growth factor: synthesis and deposition into subendothelial extracellular matrix. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[18]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[19]  T. Kurokawa,et al.  Cloning and expression of cDNA encoding human basic fibroblast growth factor , 1987, FEBS letters.

[20]  J. Fiddes,et al.  Human basic fibroblast growth factor: nucleotide sequence and genomic organization. , 1986, The EMBO journal.

[21]  J. Fiddes,et al.  Nucleotide sequence of a bovine clone encoding the angiogenic protein, basic fibroblast growth factor. , 1986, Science.

[22]  R. Ross,et al.  A significant part of macrophage-derived growth factor consists of at least two forms of PDGF , 1985, Cell.

[23]  P. Morméde,et al.  Immunoreactive fibroblast growth factor in cells of peritoneal exudate suggests its identity with macrophage-derived growth factor. , 1985, Biochemical and biophysical research communications.

[24]  H Stein,et al.  Immunoenzymatic labeling of monoclonal antibodies using immune complexes of alkaline phosphatase and monoclonal anti-alkaline phosphatase (APAAP complexes). , 1984, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[25]  T. K. Hunt,et al.  Oxygen tension regulates the expression of angiogenesis factor by macrophages. , 1983, Science.

[26]  E. Unanue,et al.  Stimulation of nonlymphoid mesenchymal cell proliferation by a macrophage-derived growth factor. , 1981, Journal of immunology.

[27]  T. K. Hunt,et al.  Stimulation of wound blood vessel growth by wound macrophages. , 1979, The Journal of surgical research.

[28]  E. Unanue,et al.  Activated macrophages induce vascular proliferation , 1977, Nature.

[29]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[30]  O. Kawanami,et al.  The role of intraalveolar fibrosis in the process of pulmonary structural remodeling in patients with diffuse alveolar damage. , 1987, The American journal of pathology.

[31]  E. Weibel,et al.  Structural alterations of lung parenchyma in the adult respiratory distress syndrome. , 1982, Clinics in chest medicine.

[32]  R. Ross,et al.  The role of the macrophage in wound repair. A study with hydrocortisone and antimacrophage serum. , 1975, The American journal of pathology.