Cellular Plasticity of Inflammatory Myeloid Cells in the Peritoneal Foreign Body Response
Implantation of sterile foreign objects in the peritoneal cavity of an animal initiates an inflammatory response and results in encapsulation of the objects by bone marrow-derived cells. Over time, a multilayered tissue capsule develops with abundant myofibroblasts embedded in extracellular matrix....
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Published in | The American journal of pathology Vol. 176; no. 1; pp. 369 - 380 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Bethesda, MD
Elsevier Inc
2010
ASIP American Society for Investigative Pathology |
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Abstract | Implantation of sterile foreign objects in the peritoneal cavity of an animal initiates an inflammatory response and results in encapsulation of the objects by bone marrow-derived cells. Over time, a multilayered tissue capsule develops with abundant myofibroblasts embedded in extracellular matrix. The present study used the transgenic MacGreen mouse to characterize the time-dependent accumulation of monocyte subsets and neutrophilic granulocytes in the inflammatory infiltrate and within the tissue capsule by their differential expression of the csf1r -EGFP transgene, F4/80, and Ly6C. As the tissue capsule developed, enhanced green fluorescent protein-positive cells changed from rounded to spindle-shaped morphology and began to co-express the myofibroblast marker α-smooth muscle actin. Expression increased with time: at day 14, 11.13 ± 0.67% of tissue capsule cells co-expressed these markers, compared with 50.77 ± 12.85% of cells at day 28. The importance of monocyte/macrophages in tissue capsule development was confirmed by clodronate-encapsulated liposome removal, which resulted in almost complete abrogation of capsule development. These results confirm the importance of monocyte/macrophages in the tissue response to sterile foreign objects implanted in the peritoneal cavity. In addition, the in vivo plasticity of peritoneal macrophages and their ability to transdifferentiate from a myeloid to mesenchymal phenotype is demonstrated. |
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AbstractList | Implantation of sterile foreign objects in the peritoneal cavity of an animal initiates an inflammatory response and results in encapsulation of the objects by bone marrow-derived cells. Over time, a multilayered tissue capsule develops with abundant myofibroblasts embedded in extracellular matrix. The present study used the transgenic MacGreen mouse to characterize the time-dependent accumulation of monocyte subsets and neutrophilic granulocytes in the inflammatory infiltrate and within the tissue capsule by their differential expression of the
csf1r
-EGFP transgene, F4/80, and Ly6C. As the tissue capsule developed, enhanced green fluorescent protein-positive cells changed from rounded to spindle-shaped morphology and began to co-express the myofibroblast marker α-smooth muscle actin. Expression increased with time: at day 14, 11.13 ± 0.67% of tissue capsule cells co-expressed these markers, compared with 50.77 ± 12.85% of cells at day 28. The importance of monocyte/macrophages in tissue capsule development was confirmed by clodronate-encapsulated liposome removal, which resulted in almost complete abrogation of capsule development. These results confirm the importance of monocyte/macrophages in the tissue response to sterile foreign objects implanted in the peritoneal cavity. In addition, the
in vivo
plasticity of peritoneal macrophages and their ability to transdifferentiate from a myeloid to mesenchymal phenotype is demonstrated. Implantation of sterile foreign objects in the peritoneal cavity of an animal initiates an inflammatory response and results in encapsulation of the objects by bone marrow-derived cells. Over time, a multilayered tissue capsule develops with abundant myofibroblasts embedded in extracellular matrix. The present study used the transgenic MacGreen mouse to characterize the time-dependent accumulation of monocyte subsets and neutrophilic granulocytes in the inflammatory infiltrate and within the tissue capsule by their differential expression of the csf1r -EGFP transgene, F4/80, and Ly6C. As the tissue capsule developed, enhanced green fluorescent protein-positive cells changed from rounded to spindle-shaped morphology and began to co-express the myofibroblast marker α-smooth muscle actin. Expression increased with time: at day 14, 11.13 ± 0.67% of tissue capsule cells co-expressed these markers, compared with 50.77 ± 12.85% of cells at day 28. The importance of monocyte/macrophages in tissue capsule development was confirmed by clodronate-encapsulated liposome removal, which resulted in almost complete abrogation of capsule development. These results confirm the importance of monocyte/macrophages in the tissue response to sterile foreign objects implanted in the peritoneal cavity. In addition, the in vivo plasticity of peritoneal macrophages and their ability to transdifferentiate from a myeloid to mesenchymal phenotype is demonstrated. Implantation of sterile foreign objects in the peritoneal cavity of an animal initiates an inflammatory response and results in encapsulation of the objects by bone marrow-derived cells. Over time, a multilayered tissue capsule develops with abundant myofibroblasts embedded in extracellular matrix. The present study used the transgenic MacGreen mouse to characterize the time-dependent accumulation of monocyte subsets and neutrophilic granulocytes in the inflammatory infiltrate and within the tissue capsule by their differential expression of the csf1r-EGFP transgene, F4/80, and Ly6C. As the tissue capsule developed, enhanced green fluorescent protein-positive cells changed from rounded to spindle-shaped morphology and began to co-express the myofibroblast marker alpha-smooth muscle actin. Expression increased with time: at day 14, 11.13 +/- 0.67% of tissue capsule cells co-expressed these markers, compared with 50.77 +/- 12.85% of cells at day 28. The importance of monocyte/macrophages in tissue capsule development was confirmed by clodronate-encapsulated liposome removal, which resulted in almost complete abrogation of capsule development. These results confirm the importance of monocyte/macrophages in the tissue response to sterile foreign objects implanted in the peritoneal cavity. In addition, the in vivo plasticity of peritoneal macrophages and their ability to transdifferentiate from a myeloid to mesenchymal phenotype is demonstrated. |
Author | Mooney, Jane E Sester, David P Hume, David A Campbell, Julie H van Rooijen, Nico Rolfe, Barbara E Osborne, Geoffrey W Campbell, Gordon R |
AuthorAffiliation | The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Roslin, Scotland, United Kingdom Centre for Research in Vascular Biology, University of Queensland, St. Lucia, Australia Department of Molecular Cell Biology, Free University Medical Centre, Amsterdam, The Netherlands Australian Institute for Bioengineering and Nanotechnology, the Queensland Brain Institute, University of Queensland, St. Lucia, Australia School of Biomedical Sciences, University of Queensland, St. Lucia, Australia |
AuthorAffiliation_xml | – name: School of Biomedical Sciences, University of Queensland, St. Lucia, Australia – name: Centre for Research in Vascular Biology, University of Queensland, St. Lucia, Australia – name: Department of Molecular Cell Biology, Free University Medical Centre, Amsterdam, The Netherlands – name: Australian Institute for Bioengineering and Nanotechnology, the Queensland Brain Institute, University of Queensland, St. Lucia, Australia – name: The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Roslin, Scotland, United Kingdom |
Author_xml | – sequence: 1 fullname: Mooney, Jane E – sequence: 2 fullname: Rolfe, Barbara E – sequence: 3 fullname: Osborne, Geoffrey W – sequence: 4 fullname: Sester, David P – sequence: 5 fullname: van Rooijen, Nico – sequence: 6 fullname: Campbell, Gordon R – sequence: 7 fullname: Hume, David A – sequence: 8 fullname: Campbell, Julie H |
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Keywords | Anatomic pathology Plasticity Foreign body Inflammation Inflammatory cell Myeloid cell Peritoneum |
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SubjectTerms | Animals Biological and medical sciences Cell Movement Cell Shape Cell Transdifferentiation Female Fibroblasts - cytology Foreign Bodies - pathology Foreign-Body Reaction - pathology Green Fluorescent Proteins - metabolism Implants, Experimental Investigative techniques, diagnostic techniques (general aspects) Macrophages - cytology Male Medical sciences Mice Myeloid Cells - pathology Pathology Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Peritoneal Cavity - pathology Peritoneal Lavage Regular |
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Title | Cellular Plasticity of Inflammatory Myeloid Cells in the Peritoneal Foreign Body Response |
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