Cited by 729Tissue Engineering and Regenerative MedicineWound Healing and TreatmentsBone Tissue Engineering Materials

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Macrophage Phenotype as a Determinant of Biologic Scaffold Remodeling

Badylak, Stephen F., Valentin, Jolene E., Ravindra, Anjani K., McCabe, George P., Stewart-Akers, Ann M.·2008·Tissue Engineering Part A

DOI 10.1089/ten.tea.2007.0264

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Abstract

Macrophage phenotype can be characterized as proinflammatory (M1) or immunomodulatory and tissue remodeling (M2). The present study used a rat model to determine the macrophage phenotype at the site of implantation of two biologic scaffolds that were derived from porcine small intestinal submucosa (SIS) and that differed mainly according to their method of processing: the Restore device (SIS) and the CuffPatch device (carbodiimide crosslinked form of porcine-derived SIS (CDI-SIS)). An autologous tissue graft was used as a control implant. Immunohistologic methods were used to identify macrophage surface markers CD68 (pan macrophages), CD80 and CCR7 (M1 profile), and CD163 (M2 profile) during the remodeling process. All graft sites were characterized by the dense population of CD68+ mononuclear cells present during the first 4 weeks. The SIS device elicited a predominantly CD163+ response (M2 profile, p < 0.001) and showed constructive remodeling at 16 weeks. The CDI-SIS device showed a predominately CD80+ and CCR7+ response (M1 profile, p < 0.03), and at 16 weeks was characterized by chronic inflammation. The autologous tissue graft showed a predominately CD163+ response (M2) at 1 week, with a dual M1/M2 population (CD80+, CCR7+, and CD163+) by 2 and 4 weeks and moderately well organized connective tissue by 16 weeks. The processing methods used during the manufacturing of a biologic scaffold can have a profound influence upon the macrophage phenotype profile and downstream remodeling events. Routine histologic examination alone is inadequate to determine the phenotype of mononuclear cells that participate in the host response to the scaffold.

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Only a specific subset of human peripheral-blood monocytes has endothelial-like functional capacity
Elsheikh, E. B., Uzunel, M., He, Z., Holgersson, J., Nowak, G., & Sumitran–Holgersson, S. (2005) · Blood · doi:10.1182/blood-2005-04-1407 · Cited by 114
Retracted
The chemokine system in diverse forms of macrophage activation and polarization
MANTOVANI, A., SICA, A., SOZZANI, S., ALLAVENA, P., VECCHI, A., & LOCATI, M. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.015 · Cited by 6,534
Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes
MANTOVANI, A., SOZZANI, S., LOCATI, M., ALLAVENA, P., & SICA, A. (2002) · Trends in Immunology · doi:10.1016/s1471-4906(02)02302-5 · Cited by 5,528
Monocyte and macrophage heterogeneity
Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190
Foreign body reaction to biomaterials
Anderson, J. M., Rodriguez, A., & Chang, D. T. (2008) · Seminars in Immunology · doi:10.1016/j.smim.2007.11.004 · Cited by 5,138 · cited 1×
“2 However, phenotypic and functional polarization of the mononuclear phagocyte cell population has recently been described, 3–6 which is similar to the Th1/Th2 polarization scheme of lymphocytes.”
Biomaterials Science: An Introduction to Materials in Medicine
Ratner, B. D., Hoffman, A. S., Schöen, F. J., & Lemons, J. E. (1996) · doi:10.1016/c2009-0-02433-7 · Cited by 5,125
M-1/M-2 Macrophages and the Th1/Th2 Paradigm
Mills, C. D., Kincaid, K., Alt, J. M., Heilman, M. J., & Hill, A. M. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.12.6166 · Cited by 3,287
The many faces of macrophage activation
Mosser, D. M. (2003) · Journal of Leukocyte Biology · doi:10.1189/jlb.0602325 · Cited by 1,902
Biological Responses to Materials
Anderson, J. M. (2001) · Annual Review of Materials Research · doi:10.1146/annurev.matsci.31.1.81 · Cited by 1,465
Macrophage Polarization Comes of Age
Mantovani, Sica, & Locati, M. (2005) · Immunity · doi:10.1016/j.immuni.2005.10.001 · Cited by 1,259

Show all 51 references

Research works printed but not linked: 1

16. Burke, B., and Lewis, C.E., eds. The Macrophage. Oxford: Oxford University Press, 2002.

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Fishman, J. M., Wiles, K., & Wood, K. J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800196-7.00008-6 · Cited by 31
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Authors: Badylak, S. F., Valentin, J. E., Ravindra, A. K., McCabe, G. P., & Stewart-Akers, A. M.
Affiliations: University of Pittsburgh (US)
Purdue University West Lafayette (US)
McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Corresponding author: Badylak, Stephen F.
ORCID: Badylak, Stephen F.
McCabe, George P.
Venue: Tissue Engineering Part A
Publisher: SAGE Publications
Published: 2008-11
Volume: 14
Issue: 11
Pages: 1835-1842
ISSN: 1937-3341 (ISSN-L)
1937-335X
DOI: 10.1089/ten.tea.2007.0264
OpenAlex: W2042569529
Cited by: 729
References: 51
Citations by year: 2026: 14 · 2025: 20 · 2024: 31 · 2023: 25 · 2022: 28 · 2021: 50 · 2020: 49 · 2019: 46 · 2018: 41 · 2017: 67 · 2016: 62 · 2015: 47 · 2014: 71 · 2013: 63 · 2012: 34
FWCI: 28.12
Type: journal article
Language: en
Open access: closed
Licence: www.liebertpub.com/nv/resources-tools/text-and-data-mining-policy/121/ (tdm)
Locations: Tissue Engineering Part A (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR054940)
Topics: Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
Health Sciences › Medicine › Surgery › Wound Healing and Treatments
Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
Keywords: macrophage phenotype, M1/M2 macrophages, porcine small intestinal submucosa, carbodiimide crosslinking, chronic inflammation, CD163, CD80, CCR7, CD68, tissue grafts
MeSH terms: CD163 Antigen, Animals, Immunohistochemistry, Macrophages, Random Allocation, Receptors, Cell Surface, Swine, Antigens, Differentiation, Myelomonocytic, Antigens, CD, Rats, Sprague-Dawley, B7-1 Antigen, Tissue Engineering, Rats, Receptors, CCR7, Tissue Scaffolds

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Macrophage Phenotype as a Determinant of Biologic Scaffold Remodeling

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