Peripheral Blood Fibrocytes: Differentiation Pathway and Migration to Wound Sites
Abstract
Fibrocytes are a distinct population of blood-borne cells that display a unique cell surface phenotype (collagen I+/CD11b+/CD13+/CD34+/CD45RO+/MHC class II+/CD86+) and exhibit potent immunostimulatory activities. Circulating fibrocytes rapidly enter sites of tissue injury, suggesting an important role for these cells in wound repair. However, the regulatory processes that govern the differentiation of blood-borne fibrocytes and the mechanisms that underlie the migration of these cells to wound sites are currently not known. We report herein that ex vivo cultured fibrocytes can differentiate from a CD14+-enriched mononuclear cell population and that this process requires contact with T cells. Furthermore, we demonstrate that TGF-β1 (1–10 ng/ml), an important fibrogenic and growth-regulating cytokine involved in wound healing, increases the differentiation and functional activity of cultured fibrocytes. Because fibrocytes home to sites of tissue injury, we examined the role of chemokine/chemokine receptor interactions in fibrocyte trafficking. We show that secondary lymphoid chemokine, a ligand of the CCR7 chemokine receptor, acts as a potent stimulus for fibrocyte chemotaxis in vitro and for the homing of injected fibrocytes to sites of cutaneous tissue injury in vivo. Finally, we demonstrate that differentiated, cultured fibrocytes express α smooth muscle actin and contract collagen gels in vitro, two characteristic features of wound-healing myofibroblasts. These data provide important insight into the control of fibrocyte differentiation and trafficking during tissue repair and significantly expand their potential role during wound healing.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Fibrocyte migration to wounds is guided by DAMPs and chemokines such as CCL21.
“Their migration to wounds is guided by damage associated molecular patterns (DAMPs) and chemokines such as Chemokine (C-C motif) ligand 21 (CCL21) (86), and after arrival, these cells start differentiating into a myofibroblast-like phenotype under the influence of factors such as TGFβ (86).”
From Unraveling SSc Pathophysiology; The Myofibroblast (2018) · cites this paper as [86]
After arrival, fibrocytes start differentiating into a myofibroblast-like phenotype under the influence of factors such as TGFβ.
“Their migration to wounds is guided by damage associated molecular patterns (DAMPs) and chemokines such as Chemokine (C-C motif) ligand 21 (CCL21) (86), and after arrival, these cells start differentiating into a myofibroblast-like phenotype under the influence of factors such as TGFβ (86).”
From Unraveling SSc Pathophysiology; The Myofibroblast (2018) · cites this paper as [86]
Cites
A highly efficacious lymphocyte chemoattractant, stromal cell-derived factor 1 (SDF-1)
Bleul, C. C., Fuhlbrigge, R. C., Casasnovas, J. M., Aiuti, A., & Springer, T. A. (1996) · The Journal of experimental medicine · doi:10.1084/jem.184.3.1101 · Cited by 1,482 · see citing works
Circulating Fibrocytes Define a New Leukocyte Subpopulation That Mediates Tissue Repair
Bucala, R., Spiegel, L. A., Chesney, J. A., Hogan, M. M., & Cerami, A. (1994) · Molecular Medicine · doi:10.1007/bf03403533 · Cited by 1,307 · see citing works
Self-citationCD14+ blood monocytes can differentiate into functionally mature CD83+ dendritic cells.
Zhou, L., & Tedder, T. F. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.6.2588 · Cited by 1,090 · see citing works
Sime, P. J., Xing, Z., Graham, F. L., Csaky, K. G., & Gauldie, J. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119590 · Cited by 1,050 · see citing works
Gunn, M. D., Kyuwa, S., Tam‐Amersdorfer, C., Kakiuchi, T., Matsuzawa, A., Williams, L. T., & Nakano, H. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.3.451 · Cited by 1,019 · see citing works
Myofibroblasts. I. Paracrine cells important in health and disease
Powell, D. W., Mifflin, R. C., Valentich, J. D., Crowe, S. E., Saada, J. I., & West, A. B. (1999) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1999.277.1.c1 · Cited by 964 · see citing works
Saeki, H., Moore, A. M., Brown, M. J., & Hwang, S. T. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.5.2472 · Cited by 623 · see citing works
Mechanisms of Myofibroblast Activity and Phenotypic Modulation
Serini, G., & Gabbiani, G. (1999) · Experimental Cell Research · doi:10.1006/excr.1999.4543 · Cited by 592 · see citing works
Branton, M., & Kopp, J. (1999) · Microbes and Infection · doi:10.1016/s1286-4579(99)00250-6 · Cited by 574 · see citing works
Vaughan, M. B., Howard, E. W., & Tomasek, J. J. (2000) · Experimental Cell Research · doi:10.1006/excr.2000.4869 · Cited by 469 · see citing works
Arora, P. D., Narani, N., & McCulloch, C. A. (1999) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)65334-5 · Cited by 465 · see citing works
Overproduction of Th2-specific chemokines in NC/Nga mice exhibiting atopic dermatitis–like lesions
Vestergaard, C., Yoneyama, H., Murai, M., Nakamura, K., Tamaki, K., Terashima, Y., Imai, T., Yoshie, O., Irimura, T., Mizutani, H., et al. (1999) · Journal of Clinical Investigation · doi:10.1172/jci7613 · Cited by 406 · see citing works
Pickl, W. F., Majdic, O., Kohl, P., Stöckl, J., Riedl, E., Scheinecker, C., Bello-Fernández, C., & Knapp, W. (1996) · The Journal of Immunology · doi:10.4049/jimmunol.157.9.3850 · Cited by 399 · see citing works
Regulated Production of Type I Collagen and Inflammatory Cytokines by Peripheral Blood Fibrocytes
Chesney, J. A., Metz, C. N., Stavitsky, A. B., Bacher, M., & Bucala, R. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.160.1.419 · Cited by 371 · see citing works
Self-citationInhibition of Myofibroblast Apoptosis by Transforming Growth Factor β1
Zhang, H. Y., & Phan, S. H. (1999) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/ajrcmb.21.6.3720 · Cited by 354 · see citing works
Chesney, J. A., Bacher, M., Bender, A., & Bucala, R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.12.6307 · Cited by 343 · see citing works
Self-citationDifferentiation of human dendritic cells from monocytes in vitro
Chapuis, F., Rosenzwajg, M., Yagello, M., Ekman, M., Biberfeld, P., & Gluckman, J. C. (1997) · European Journal of Immunology · doi:10.1002/eji.1830270213 · Cited by 338 · see citing works
McCormick, L. L., Zhang, Y., Tootell, E., & Gilliam, A. C. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.10.5693 · Cited by 264 · see citing works
Matsuda, H., Koyama, H., Sato, H., Sawada, J., Itakura, A., Tanaka, A., Matsumoto, M., Konno, K., Ushio, H., & Matsuda, K. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.187.3.297 · Cited by 242 · see citing works
Kaliński, P., Schuitemaker, J. H. N., Hilkens, C. M. U., Wierenga, E. A., & Kapsenberg, M. L. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.6.3231 · Cited by 211 · see citing works
Lymphoid Tissue Homing Chemokines Are Expressed in Chronic Inflammation
Hjelmström, P., Fjell, J., Nakagawa, T., Sacca, R. E., Cuff, C. A., & Ruddle, N. H. (2000) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64981-4 · Cited by 195 · see citing works
Nakano, H., Mori, S., Yonekawa, H., Nariuchi, H., Matsuzawa, A., & Kakiuchi, T. (1998) · Blood · doi:10.1182/blood.v91.8.2886.2886_2886_2895 · Cited by 184 · see citing works
The Role of α1β1 Integrin in Wound Contraction
Racine-Samson, L., Rockey, D. C., & Bissell, D. M. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.49.30911 · Cited by 176 · see citing works
Transforming growth factor β levels in rat wound chambers
Cromack, D. T., Sporn, M. B., Roberts, A. B., Merino, M. J., Dart, L. L., & Norton, J. A. (1987) · Journal of Surgical Research · doi:10.1016/0022-4804(87)90005-9 · Cited by 159 · see citing works
Pivotal role of TARC, a CC chemokine, in bacteria-induced fulminant hepatic failure in mice.
Yoneyama, H., Harada, A., Imai, T., Baba, M., Yoshie, O., Zhang, Y., Higashi, H., Murai, M., Asakura, H., & Matsushima, K. (1998) · Journal of Clinical Investigation · doi:10.1172/jci4619 · Cited by 139 · see citing works
Genetic defect in T lymphocyte‐specific homing into peripheral lymph nodes
Nakano, H., Tamura, T., Yoshimoto, T., Yagita∥, H., Miyasaka, M., Butcher, E. C., Nariuchi, H., Kakiuchi, T., & Matsuzawa, A. (1997) · European Journal of Immunology · doi:10.1002/eji.1830270132 · Cited by 137 · see citing works
Benn, S. I., Whitsitt, J. S., Broadley, K. N., Nanney, L. B., Perkins, D., He, L., Patel, M., Morgan, J. R., Swain, W. F., & Davidson, J. M. (1996) · Journal of Clinical Investigation · doi:10.1172/jci119118 · Cited by 108 · see citing works
Dendritic Cells Require T Cells for Functional Maturation In Vivo
Shreedhar, V. K., Moodycliffe, A. M., Ullrich, S. E., Bucana, C. D., Kripke, M. L., & Flores‐Romo, L. (1999) · Immunity · doi:10.1016/s1074-7613(00)80137-5 · Cited by 105 · see citing works
Gauldie, J., Sime, P. J., Xing, Z., Marr, B., & Tremblay, G. M. (1999) · Current topics in pathology · doi:10.1007/978-3-642-58456-5_5 · Cited by 93 · see citing works
Varona, R., Zaballos, Á., Gutiérrez, J., Martı́n, P., Roncal, F., Albar, J. P., Ardavı́n, C., & Márquez, G. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)01450-1 · Cited by 88 · see citing works
Fibroblast heterogeneity in physiological conditions and fibrotic disease
Jelaska, A., Strehlow, D., & Korn, J. H. (1999) · Springer Seminars in Immunopathology · doi:10.1007/bf00870301 · Cited by 76 · see citing works
Wang, X., Smith, P. D., Pu, L. L. Q., Kim, Y., Ko, F., & Robson, M. C. (1999) · Journal of Surgical Research · doi:10.1006/jsre.1999.5757 · Cited by 76 · see citing works
Arora, P. D., & McCulloch, C. A. (1999) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)65527-7 · Cited by 75 · see citing works
Chesney, J. A., & Bucala, R. (1997) · Biochemical Society Transactions · doi:10.1042/bst0250520 · Cited by 67 · see citing works
Self-citationThe Fibroblast — A Ubiquitous Ally for the Surgeon
Dunphy, J. E. (1963) · New England Journal of Medicine · doi:10.1056/nejm196306202682501 · Cited by 62 · see citing works
Chu, A. J., & Prasad, J. K. (1999) · Journal of the American College of Surgeons · doi:10.1016/s1072-7515(98)00303-2 · Cited by 45 · see citing works
Grab, D. J., Lanners, H. N., Martin, L. N., Chesney, J. A., Cai, C., Adkisson, H. D., & Bucala, R. (1999) · Molecular Medicine · doi:10.1007/bf03402138 · Cited by 45 · see citing works
Self-citationXu, H., Kramer, M. M., Spengler, H., & Peters, J. H. (1995) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-1971-3_15 · Cited by 43 · see citing works
Chemokine Amplification in Mesangial Cells
Luo, Y., Lloyd, C. M., Gutierrez-Ramos, J.-C., & Dorf, M. E. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.7.3985 · Cited by 39 · see citing works
Adachi, S., Ito, H., Tamamori, M., Tanaka, M., Marumo, F., & Hiroe, M. (1998) · Life Sciences · doi:10.1016/s0024-3205(98)00452-4 · Cited by 30 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Epithelial-mesenchymal transition and its implications for fibrosis
Kalluri, R., & Neilson, E. G. (2003) · Journal of Clinical Investigation · doi:10.1172/jci20530 · Cited by 2,651 · see citing works
Nathan, C., & Ding, A. (2010) · Cell · doi:10.1016/j.cell.2010.02.029 · Cited by 2,183 · see citing works
Hinz, B., Phan, S. H., Thannickal, V. J., Galli, A., Bochaton-Piallat, M.-L., & Gabbiani, G. (2007) · The American Journal of Pathology · doi:10.2353/ajpath.2007.070112 · Cited by 2,068 · see citing works
Molecular and cellular mechanisms of liver fibrosis and its regression
Kisseleva, T., & Brenner, D. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-00372-7 · Cited by 2,024 · see citing works
Transition from inflammation to proliferation: a critical step during wound healing
Landén, N. X., Li, D., & Ståhle, M. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2268-0 · Cited by 1,980 · see citing works
“If the wound condition is long lasting, fibroblasts in the wounds may also originate from fibrocytes, which is a group of bone marrow-derived mesenchymal progenitor cells [37, 38].”
BackgroundEvidence that fibroblasts derive from epithelium during tissue fibrosis
Iwano, M., Plieth, D., Danoff, T. M., Xue, C., Okada, H., & Neilson, E. G. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15518 · Cited by 1,809 · see citing works
Formation and function of the myofibroblast during tissue repair
Hinz, B. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700613 · Cited by 1,658 · see citing works
Cardiac Fibrosis: The Fibroblast Awakens
Travers, J. G., Kamal, F. A., Robbins, J., Yutzey, K. E., & Blaxall, B. C. (2016) · Circulation Research · doi:10.1161/circresaha.115.306565 · Cited by 1,596 · see citing works
Evidence that fibroblasts derive from epithelium during tissue fibrosis
Iwano, M., Plieth, D., Danoff, T. M., Xue, C., Okada, H., & Neilson, E. G. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215518 · Cited by 1,589 · see citing works
Transforming growth factor–β in tissue fibrosis
Frangogiannis, N. G. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20190103 · Cited by 1,310 · see citing works
Systemic sclerosis: a prototypic multisystem fibrotic disorder
Varga, J., & Abraham, D. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31139 · Cited by 1,164 · see citing works
Circulating fibrocytes traffic to the lungs in response to CXCL12 and mediate fibrosis
Phillips, R. J., Burdick, M. D., Hong, K. M., Lutz, M., Murray, L. A., Xue, Y., Belperio, J. A., Keane, M. P., & Strieter, R. M. (2004) · Journal of Clinical Investigation · doi:10.1172/jci20997 · Cited by 1,071 · see citing works
Role of tissue stroma in cancer cell invasion
De Wever, O., & Mareel, M. (2003) · The Journal of Pathology · doi:10.1002/path.1398 · Cited by 1,042 · see citing works
Fibroblasts and myofibroblasts in wound healing
Desmouliere, A., Darby, I. A., Laverdet, B., & Bonté, F. (2014) · Clinical, Cosmetic and Investigational Dermatology · doi:10.2147/ccid.s50046 · Cited by 1,039 · see citing works
Rock, J. R., Barkauskas, C. E., Cronce, M. J., Xue, Y., Harris, J. R., Liang, J., Noble, P. W., & Hogan, B. L. M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117988108 · Cited by 1,033 · see citing works
Souders, C. A., Bowers, S., & Baudino, T. A. (2009) · Circulation Research · doi:10.1161/circresaha.109.209809 · Cited by 978 · see citing works
Structural and functional characterisation of cardiac fibroblasts
Camelliti, P., Borg, T. K., & Kohl, P. K. (2004) · Cardiovascular Research · doi:10.1016/j.cardiores.2004.08.020 · Cited by 929 · see citing works
Perspective Article: Tissue repair, contraction, and the myofibroblast
Desmoulière, A., Chaponnier, C., & Gabbiani, G. (2005) · Wound Repair and Regeneration · doi:10.1111/j.1067-1927.2005.130102.x · Cited by 892 · see citing works
Lin, S., Kisseleva, T., Brenner, D. A., & Duffield, J. S. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.080433 · Cited by 834 · see citing works
Pulmonary fibrosis: pathogenesis, etiology and regulation
Wilson, M. S., & Wynn, T. A. (2009) · Mucosal Immunology · doi:10.1038/mi.2008.85 · Cited by 821 · see citing works
Wound healing, fibroblast heterogeneity, and fibrosis
Talbott, H. E., Mascharak, S., Griffin, M., Wan, D. C., & Longaker, M. (2022) · Cell Stem Cell · doi:10.1016/j.stem.2022.07.006 · Cited by 745 · see citing works
Metcalfe, A. D., & Ferguson, M. W. J. (2006) · Journal of The Royal Society Interface · doi:10.1098/rsif.2006.0179 · Cited by 786 · see citing works
Wound healing and the role of fibroblasts
Bainbridge, P. (2013) · Journal of Wound Care · doi:10.12968/jowc.2013.22.8.407 · Cited by 783 · see citing works
Shaw, T. J., & Martin, P. B. (2009) · Journal of Cell Science · doi:10.1242/jcs.031187 · Cited by 771 · see citing works
Mesenchymal Stem Cells as Therapeutics
Parekkadan, B., & Milwid, J. M. (2010) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-070909-105309 · Cited by 758 · see citing works
Bone marrow–derived progenitor cells in pulmonary fibrosis
Hashimoto, N., Jin, H., Liu, T., Chensue, S. W., & Phan, S. H. (2004) · Journal of Clinical Investigation · doi:10.1172/jci18847 · Cited by 715 · see citing works
Identification of Circulating Fibrocytes as Precursors of Bronchial Myofibroblasts in Asthma
Schmidt, M., Sun, G. Y., Stacey, M. A., Mori, L., & Mattoli, S. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.1.380 · Cited by 633 · see citing works
Fibroblasts and myofibroblasts in wound healing: Force generation and measurement
Li, B., & Wang, J. H.-C. (2011) · Journal of Tissue Viability · doi:10.1016/j.jtv.2009.11.004 · Cited by 594 · see citing works
Fibroblast Differentiation in Wound Healing and Fibrosis
Darby, I. A., & Hewitson, T. D. (2007) · International review of cytology · doi:10.1016/s0074-7696(07)57004-x · Cited by 605 · see citing works
The origin of fibroblasts and mechanism of cardiac fibrosis
Krenning, G., Zeisberg, E. M., & Kalluri, R. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22322 · Cited by 601 · see citing works
Epithelial-mesenchymal transition in tissue repair and fibrosis
Stone, R. C., Pastar, I., Ojeh, N. O., Chen, V., Liu, S., Garzon, K. I., & Tomic‐Canic, M. (2016) · Cell and Tissue Research · doi:10.1007/s00441-016-2464-0 · Cited by 577 · see citing works
The stroma reaction myofibroblast: a key player in the control of tumor cell behavior
Desmoulière, A., Guyot, C., & Gabbiani, G. (2004) · The International Journal of Developmental Biology · doi:10.1387/ijdb.041802ad · Cited by 551 · see citing works
Bone marrow contribution to tumor-associated myofibroblasts and fibroblasts
Direkze, N. C., Hodivala-Dilke, K., Jeffery, R., Hunt, T., Poulsom, R., Oukrif, D., Alison, M. R., & Wright, N. A. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-1708 · Cited by 530 · see citing works
Circulating fibrocytes: collagen-secreting cells of the peripheral blood
Quan, T. E., Cowper, S. E., Wu, S.-P., Bockenstedt, L. K., & Bucala, R. (2003) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2003.10.005 · Cited by 527 · see citing works
Self-citationMack, M. (2017) · Matrix Biology · doi:10.1016/j.matbio.2017.11.010 · Cited by 516 · see citing works
Circulating Fibrocytes Are an Indicator of Poor Prognosis in Idiopathic Pulmonary Fibrosis
Moeller, A., Gilpin, S. E., Ask, K., Cox, G., Cook, D., Gauldie, J., Margetts, P. J., Farkas, L., Dobranowski, J., Boylan, C., et al. (2009) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200810-1534oc · Cited by 513 · see citing works
Contribution of Bone Marrow–Derived Cells to Skin: Collagen Deposition and Wound Repair
Fathke, C., Wilson, L., Hutter, J., Kapoor, V., Smith, A. N., Hocking, A. M., & Isik, F. F. (2004) · Stem Cells · doi:10.1634/stemcells.22-5-812 · Cited by 490 · see citing works
Pilling, D., Fan, T., Huang, D. S., Kaul, B., & Gomer, R. H. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007475 · Cited by 487 · see citing works
Greaves, N., Ashcroft, K., Baguneid, M., & Bayat, A. (2013) · Journal of dermatological science (Amsterdam) · doi:10.1016/j.jdermsci.2013.07.008 · Cited by 462 · see citing works
Oxidative stress and glutathione in TGF-β-mediated fibrogenesis
Liu, R.-M., & Pravia, K. A. G. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.09.026 · Cited by 468 · see citing works
Bone marrow-derived fibrocytes participate in pathogenesis of liver fibrosis
Kisseleva, T., Uchinami, H., Feirt, N. M., Bustamante, O. Q., Segovia, J. C., Schwabe, R. F., & Brenner, D. A. (2006) · Journal of Hepatology · doi:10.1016/j.jhep.2006.04.014 · Cited by 469 · see citing works
Fibroblasts and myofibroblasts: Their source, function and role in disease
McAnulty, R. J. (2006) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2006.11.005 · Cited by 455 · see citing works
Li, Y., Foster, W. H., Deasy, B. M., Chan, Y., Prisk, V. R., Tang, Y., Cummins, J. H., & Huard, J. (2004) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63188-4 · Cited by 454 · see citing works
CCR2-Mediated Recruitment of Fibrocytes to the Alveolar Space after Fibrotic Injury
Moore, B. B., Kolodsick, J. E., Thannickal, V. J., Cooke, K. R., Moore, T. A., Hogaboam, C. M., Wilke, C. A., & Toews, G. B. (2005) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)62289-4 · Cited by 440 · see citing works
Mechanisms of liver fibrosis and its role in liver cancer
Dhar, D., Baglieri, J., Kisseleva, T., & Brenner, D. A. (2020) · Experimental Biology and Medicine · doi:10.1177/1535370219898141 · Cited by 440 · see citing works
Cardiac fibroblasts: friend or foe?
Baudino, T. A., Carver, W., Giles, W., & Borg, T. K. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00023.2006 · Cited by 427 · see citing works
Bellini, A., & Mattoli, S. (2007) · Laboratory Investigation · doi:10.1038/labinvest.3700654 · Cited by 421 · see citing works
Synovial cell cross-talk with cartilage plays a major role in the pathogenesis of osteoarthritis
Chou, C.-H., Jain, V., Gibson, J., Attarian, D. E., Haraden, C. A., Yohn, C. B., Laberge, R.-M., Gregory, S., & Kraus, V. B. (2020) · Scientific Reports · doi:10.1038/s41598-020-67730-y · Cited by 398 · see citing works
Lech, M., & Anders, H. (2013) · Biochimica et Biophysica Acta · doi:10.1016/j.bbadis.2012.12.001 · Cited by 424 · see citing works
Mesenchymal Cells of the Intestinal Lamina Propria
Powell, D. W., Pinchuk, I. V., Saada, J. I., Chen, X., & Mifflin, R. C. (2011) · Annual Review of Physiology · doi:10.1146/annurev.physiol.70.113006.100646 · Cited by 388 · see citing works
Cytokine mediated tissue fibrosis
Borthwick, L. A., Wynn, T. A., & Fisher, A. J. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2012.09.014 · Cited by 375 · see citing works
Rats and mice exhibit distinct inflammatory reactions after spinal cord injury
Sroga, J. M., Jones, T. B., Kigerl, K. A., McGaughy, V. M., & Popovich, P. G. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10736 · Cited by 369 · see citing works
Desmoulière, A., Darby, I. A., & Gabbiani, G. (2003) · Laboratory Investigation · doi:10.1097/01.lab.0000101911.53973.90 · Cited by 364 · see citing works
Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosis
Andersson‐Sjöland, A., de Alba, C. G., Nihlberg, K., Becerril, C., Ramı́rez, R., Pardo, A., Westergren‐Thorsson, G., & Selman, M. (2008) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2008.02.012 · Cited by 360 · see citing works
Potential cellular and molecular causes of hypertrophic scar formation
van der Veer, W. M., Bloemen, M. C. T., Ulrich, M. M. W., Molema, G., van Zuijlen, P. P. M., Middelkoop, E., & Niessen, F. B. (2008) · Burns · doi:10.1016/j.burns.2008.06.020 · Cited by 356 · see citing works
Molecular pathology of wound healing
Kondo, T., & Ishida, Y. (2010) · Forensic Science International · doi:10.1016/j.forsciint.2010.07.004 · Cited by 347 · see citing works
Fibroblasts and myofibroblasts in renal fibrosis
Meran, S., & Steadman, R. (2011) · International Journal of Experimental Pathology · doi:10.1111/j.1365-2613.2011.00764.x · Cited by 345 · see citing works
Origin of myofibroblasts and cellular events triggering fibrosis
Mack, M., & Yanagita, M. (2014) · Kidney International · doi:10.1038/ki.2014.287 · Cited by 344 · see citing works
Yamada, M., Kubo, H., Kobayashi, S., Ishizawa, K., Numasaki, M., Ueda, S., SUZUKI, T. A., & Sasaki, H. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.2.1266 · Cited by 341 · see citing works
Baglieri, J., Brenner, D. A., & Kisseleva, T. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20071723 · Cited by 341 · see citing works
Bone marrow-derived fibroblast precursors mediate ischemic cardiomyopathy in mice
Haudek, S. B., Xia, Y., Huebener, P., Lee, J. M., Carlson, S., Crawford, J. R., Pilling, D., Gomer, R. H., Trial, J., Frangogiannis, N. G., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608799103 · Cited by 339 · see citing works
The reactive stroma microenvironment and prostate cancer progression
Barron, D. A., & Rowley, D. R. (2012) · Endocrine Related Cancer · doi:10.1530/erc-12-0085 · Cited by 331 · see citing works
Varga, J., Trojanowska, M. E., & Kuwana, M. (2017) · Journal of Scleroderma and Related Disorders · doi:10.5301/jsrd.5000249 · Cited by 323 · see citing works
Cellular mechanisms of skin repair in humans and other mammals
Rittié, L. (2016) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-016-0330-1 · Cited by 326 · see citing works
The Pathogenesis of Systemic Sclerosis
Katsumoto, T. R., Whitfield, M. L., & Connolly, M. K. (2011) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-011110-130312 · Cited by 319 · see citing works
The Role of CCL12 in the Recruitment of Fibrocytes and Lung Fibrosis
Moore, B. B., Murray, L. A., Das, A., Wilke, C. A., Herrygers, A. B., & Toews, G. B. (2006) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2005-0239oc · Cited by 309 · see citing works
Inhibition of Fibrocyte Differentiation by Serum Amyloid P 1
Pilling, D., Buckley, C., Salmon, M., & Gomer, R. (2003) · Journal of Immunology · doi:10.4049/jimmunol.171.10.5537 · Cited by 331 · see citing works
A stromal address code defined by fibroblasts
Parsonage, G., Filer, A. D., Haworth, O., Nash, G. B., Rainger, G. E., Salmon, M., & Buckley, C. D. (2005) · Trends in Immunology · doi:10.1016/j.it.2004.11.014 · Cited by 297 · see citing works
Biology of Fibroblasts and Myofibroblasts
Phan, S. H. (2008) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200708-146dr · Cited by 296 · see citing works
Tumor Microenvironment in Head and Neck Squamous Cell Carcinoma
Curry, J., Sprandio, J. D., Cognetti, D. M., Luginbuhl, A., Bar‐Ad, V., Pribitkin, E. A., & Tuluc, M. (2014) · Seminars in Oncology · doi:10.1053/j.seminoncol.2014.03.003 · Cited by 291 · see citing works
Concise Review: Bone Marrow-Derived Stem/Progenitor Cells in Cutaneous Repair and Regeneration
Wu, Y., Zhao, R. C., & Tredget, E. E. (2010) · Stem Cells · doi:10.1002/stem.420 · Cited by 284 · see citing works
Concise Review: Multipotent Mesenchymal Stromal Cells in Blood
He, Q., Wan, C., & Li, G. (2006) · Stem Cells · doi:10.1634/stemcells.2006-0335 · Cited by 284 · see citing works
Role of growth factors and the wound healing response in age-related macular degeneration
Schlingemann, R. O. (2003) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-003-0828-0 · Cited by 284 · see citing works
New Mechanisms of Pulmonary Fibrosis
Strieter, R. M., & Mehrad, B. (2009) · CHEST Journal · doi:10.1378/chest.09-0510 · Cited by 287 · see citing works
Bone-marrow-derived myofibroblasts contribute to the cancer-induced stromal reaction
Ishii, G., Sangai, T., Oda, T., Aoyagi, Y., Hasebe, T., Kanomata, N., Endoh, Y., Okumura, C., Okuhara, Y., Magae, J., et al. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)01544-4 · Cited by 281 · see citing works
Sakai, N., Wada, T., Yokoyama, H., Lipp, M., Ueha, S., Matsushima, K., & Kaneko, S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511200103 · Cited by 278 · see citing works
Mesenchymal stem cell therapy for attenuation of scar formation during wound healing
Jackson, W. M., Nesti, L. J., & Tuan, R. S. (2012) · Stem Cell Research & Therapy · doi:10.1186/scrt111 · Cited by 277 · see citing works
The role of CXC chemokines in pulmonary fibrosis
Strieter, R. M., Gomperts, B. N., & Keane, M. P. (2007) · Journal of Clinical Investigation · doi:10.1172/jci30562 · Cited by 273 · see citing works
Pivotal Advance: Th‐1 cytokines inhibit, and Th‐2 cytokines promote fibrocyte differentiation
Shao, D., Suresh, R., Vakil, V., Gomer, R., & Pilling, D. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.1107782 · Cited by 288 · see citing works
Kigerl, K. A., McGaughy, V. M., & Popovich, P. G. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20827 · Cited by 271 · see citing works
Liver fibrosis: cellular mechanisms of progression and resolution
Henderson, N. C., & Iredale, J. P. (2007) · Clinical Science · doi:10.1042/cs20060242 · Cited by 270 · see citing works
Concise Review: Clinical Translation of Wound Healing Therapies Based on Mesenchymal Stem Cells
Jackson, W. M., Nesti, L. J., & Tuan, R. S. (2011) · Stem Cells Translational Medicine · doi:10.5966/sctm.2011-0024 · Cited by 270 · see citing works
Hartlapp, I., Abe, R., Saeed, R. W., Peng, T., Voelter, W., Bucala, R., & Metz, C. N. (2001) · The FASEB Journal · doi:10.1096/fj.01-0049com · Cited by 266 · see citing works
Self-citationFibroblasts as architects of cancer pathogenesis
Marsh, T., Pietras, K., & McAllister, S. S. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2012.10.013 · Cited by 263 · see citing works
The role of circulating fibrocytes in fibrosis
Quan, T. E., Cowper, S. E., & Bucala, R. (2006) · Current Rheumatology Reports · doi:10.1007/s11926-006-0055-x · Cited by 264 · see citing works
Self-citationDefining the Cardiac Fibroblast
Ivey, M. J., & Tallquist, M. D. (2016) · Circulation Journal · doi:10.1253/circj.cj-16-1003 · Cited by 258 · see citing works
Circulating peripheral blood fibrocytes in human fibrotic interstitial lung disease
Mehrad, B., Burdick, M. D., Zisman, D. A., Keane, M. P., Belperio, J. A., & Strieter, R. M. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.11.149 · Cited by 255 · see citing works
Direct contribution of epithelium to organ fibrosis: epithelial-mesenchymal transition
Guarino, M., Tosoni, A., & Nebuloni, M. (2009) · Human Pathology · doi:10.1016/j.humpath.2009.02.020 · Cited by 255 · see citing works
The Inflammation–Fibrosis Link? A Jekyll and Hyde Role for Blood Cells during Wound Repair
Stramer, B. M., Mori, R., & Martin, P. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700811 · Cited by 251 · see citing works
Eyden, B. P. (2007) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2007.00213.x · Cited by 252 · see citing works
Sun, L., Louie, M. C., Vannella, K. M., Wilke, C. A., LeVine, A. M., Moore, B. B., & Shanley, T. P. (2010) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00122.2010 · Cited by 251 · see citing works
SPARC and tumor growth: Where the seed meets the soil?
Framson, P. E., & Sage, E. H. (2004) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20091 · Cited by 250 · see citing works
Brittan, M., Hunt, T., Jeffery, R., Poulsom, R., Forbes, S. J., Hodivala‐Dilke, K., Goldman, J. M., Alison, M. R., & Wright, N. A. (2002) · Gut · doi:10.1136/gut.50.6.752 · Cited by 250 · see citing works
Fibroblasts in the Tumor Microenvironment: Shield or Spear?
Alkasalias, T., Moyano‐Galceran, L., Arsenian‐Henriksson, M., & Lehti, K. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19051532 · Cited by 243 · see citing works
Davie, N. J., Crossno, J. T., Frid, M. G., Hofmeister, S. E., Reeves, J. Τ., Hyde, D. M., Carpenter, T. C., Brunetti, J. A., McNiece, I., & Stenmark, K. R. (2004) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00108.2003 · Cited by 249 · see citing works
Direkze, N. C., Forbes, S. J., Brittan, M., Hunt, T., Jeffery, R. E., Preston, S. L., Poulsom, R., Hodivala‐Dilke, K., Alison, M. R., & Wright, N. A. (2003) · Stem Cells · doi:10.1634/stemcells.21-5-514 · Cited by 246 · see citing works
Differentiation of Muscle-Derived Cells into Myofibroblasts in Injured Skeletal Muscle
Li, Y., & Huard, J. (2002) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64250-2 · Cited by 243 · see citing works
Origins of Cardiac Fibroblasts
Zeisberg, E. M., & Kalluri, R. (2010) · Circulation Research · doi:10.1161/circresaha.110.231910 · Cited by 243 · see citing works
Hepatic fibrosis and cirrhosis: The (myo)fibroblastic cell subpopulations involved
Guyot, C., Lepreux, S., Combe, C., Doudnikoff, É., Bioulac‐Sage, P., Balabaud, C. P., & Desmoulière, A. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.08.021 · Cited by 241 · see citing works
Yang, L., Scott, P. G., Giuffre, J. L., Shankowsky, H. A., Ghahary, A., & Tredget, E. E. (2002) · Laboratory Investigation · doi:10.1097/01.lab.0000027841.50269.61 · Cited by 239 · see citing works
- Authors
- Abe, R., Donnelly, S. C., Peng, T., Bucala, R., & Metz, C. N.
- Affiliations
- Laboratory of Vascular Biology, The Picower Institute for Medical Research , Manhasset, NY 11030
- Laboratory of Medical Biochemistry, The Picower Institute for Medical Research , Manhasset, NY 11030
- Corresponding author
- Abe, Riichiro
- Peng, Tina
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2001-06
- Volume
- 166
- Issue
- 12
- Pages
- 7556-7562
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- OpenAlex
- W4248565951
- Cited by
- 967
- References
- 40
- Citations by year
- 2026: 13 · 2025: 15 · 2024: 22 · 2023: 25 · 2022: 28 · 2021: 23 · 2020: 37 · 2019: 30 · 2018: 34 · 2017: 31 · 2016: 43 · 2015: 47 · 2014: 58 · 2013: 59 · 2012: 68
- FWCI
- 27.32
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Immunology and Microbiology › Immunology › Macrophage Migration Inhibitory Factor
- Keywords
- fibrocytes, fibrocyte differentiation, wound healing, TGF-β1, CCR7, tissue damage, myofibroblasts, alpha-smooth muscle actin, collagen gel contraction
- MeSH terms
- Animals, Blood Cells, Cell Differentiation, Cell Movement, Cells, Cultured, Collagen, Female, Fibroblasts, Fibrosis, Gels, Humans, Injections, Intravenous, Mice, Inbred BALB C, Stem Cells, Wound Healing, Transforming Growth Factor beta, Lipopolysaccharide Receptors, Receptors, Chemokine, Stem Cell Transplantation, Mice, Transforming Growth Factor beta1
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review