Infarct Fibroblasts Do Not Derive From Bone Marrow Lineages

被引:61
|
作者
Moore-Morris, Thomas [1 ]
Cattaneo, Paola [2 ,5 ,6 ]
Guimaraes-Camboa, Nuno [2 ]
Bogomolovas, Julius [3 ]
Cedenilla, Marta [7 ,8 ]
Banerjee, Indroneal [4 ]
Ricote, Mercedes [7 ]
Kisseleva, Tatiana
Zhang, Lunfeng [2 ]
Gu, Yusu [3 ]
Dalton, Nancy D. [3 ]
Peterson, Kirk L. [3 ]
Chen, Ju [3 ]
Puceat, Michel [1 ]
Evans, Sylvia M. [2 ,3 ,4 ]
机构
[1] Aix Marseille Univ, INSERM, UMR S910, GMGF, Marseille, France
[2] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[5] CNR, Inst Genet & Biomed Res, Milan Unit, Milan, Italy
[6] Humanitas Clin & Res Ctr, Rozzano, MI, Italy
[7] Ctr Nacl Invest Cardiovasc, Cardiovasc Dev & Repair Dept, Madrid, Spain
[8] Merck Sharp & Dohme Spain, Josefa Valcarcel, Spain
关键词
bone marrow; fibroblasts; fibrosis; heart diseases; myocardial infarction; CARDIAC FIBROBLASTS; MYOCARDIAL-INFARCTION; CELLS; ORIGIN; HEART; SCAR; MYOFIBROBLASTS; FIBROCYTES; CONTRIBUTE; FIBROSIS;
D O I
10.1161/CIRCRESAHA.117.311490
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: Myocardial infarction is a major cause of adult mortality worldwide. The origin(s) of cardiac fibroblasts that constitute the postinfarct scar remain controversial, in particular the potential contribution of bone marrow lineages to activated fibroblasts within the scar. Objective: The aim of this study was to establish the origin(s) of infarct fibroblasts using lineage tracing and bone marrow transplants and a robust marker for cardiac fibroblasts, the Collagen1a1-green fluorescent protein reporter. Methods and Results: Using genetic lineage tracing or bone marrow transplant, we found no evidence for collagen-producing fibroblasts derived from hematopoietic or bone marrow lineages in hearts subjected to permanent left anterior descending coronary artery ligation. In fact, fibroblasts within the infarcted area were largely of epicardial origin. Intriguingly, collagen-producing fibrocytes from hematopoietic lineages were observed attached to the epicardial surface of infarcted and sham-operated hearts in which a suture was placed around the left anterior descending coronary artery. Conclusions: In this controversial field, our study demonstrated that the vast majority of infarct fibroblasts were of epicardial origin and not derived from bone marrow lineages, endothelial-to-mesenchymal transition, or blood. We also noted the presence of collagen-producing fibrocytes on the epicardial surface that resulted at least in part from the surgical procedure.
引用
收藏
页码:583 / 590
页数:8
相关论文
共 50 条
  • [31] Bone marrow mononuclear cell therapy limits myocardial infarct size through vascular endothelial growth factor
    Hiasa, K
    Egashira, K
    Kitamoto, S
    Ishibashi, M
    Inoue, S
    Ni, WH
    Zhao, QW
    Nagata, S
    Katoh, M
    Sata, M
    Takeshita, A
    BASIC RESEARCH IN CARDIOLOGY, 2004, 99 (03) : 165 - 172
  • [32] Bone marrow mononuclear cell therapy limits myocardial infarct size through vascular endothelial growth factor
    Ken-ichi Hiasa
    Kensuke Egashira
    Shiro Kitamoto
    Minako Ishibashi
    Shujiro Inoue
    Weihua Ni
    Qingwei Zhao
    Shin Nagata
    Makoto Katoh
    Masataka Sata
    Akira Takeshita
    Basic Research in Cardiology, 2004, 99 : 165 - 172
  • [33] Sex Differences and Bone Metastases of Breast, Lung, and Prostate Cancers: Do Bone Homing Cancers Favor Feminized Bone Marrow?
    Farach-Carson, Mary C.
    Lin, Sue-Hwa
    Nalty, Theresa
    Satcher, Robert L.
    FRONTIERS IN ONCOLOGY, 2017, 7 : 163
  • [34] Infectivity in bone marrow from sporadic CJD patients
    Huor, Alvina
    Douet, Jean Yves
    Lacroux, Caroline
    Lugan, Severine
    Tillier, Cecile
    Aron, Naima
    Cassard, Herve
    Arnold, Mark
    Maria Torres, Juan
    Ironside, James W.
    Andreoletti, Olivier
    JOURNAL OF PATHOLOGY, 2017, 243 (03) : 273 - 278
  • [35] Reduction in infarct size, but no functional improvement after bone marrow cell administration in a porcine model of reperfused myocardial infarction
    Moelker, Amber D.
    Baks, Timo
    van den Bos, E. J.
    van Geuns, R. J.
    de Feyter, P. J.
    Duncker, Dirk J.
    van der Giessen, W. J.
    EUROPEAN HEART JOURNAL, 2006, 27 (24) : 3057 - 3064
  • [36] Could Cancer Initiate From Bone Marrow Progenitors?
    Ben Nasr, Hmed
    Hammami, Serria Turky
    Zeghal, Khaled
    IRANIAN JOURNAL OF CANCER PREVENTION, 2013, 6 (02) : 108 - 112
  • [37] Enhanced Effect of Combining Human Cardiac Stem Cells and Bone Marrow Mesenchymal Stem Cells to Reduce Infarct Size and to Restore Cardiac Function After Myocardial Infarction
    Williams, Adam R.
    Hatzistergos, Konstantinos E.
    Addicott, Benjamin
    McCall, Fred
    Carvalho, Decio
    Suncion, Viky
    Morales, Azorides R.
    Da Silva, Jose
    Sussman, Mark A.
    Heldman, Alan W.
    Hare, Joshua M.
    CIRCULATION, 2013, 127 (02) : 213 - 223
  • [38] EXTRACELLULAR-MATRIX GENE-EXPRESSION BY HUMAN BONE-MARROW STROMA AND BY MARROW FIBROBLASTS
    CHICHESTER, CO
    FERNANDEZ, M
    MINGUELL, JJ
    CELL ADHESION AND COMMUNICATION, 1993, 1 (02) : 93 - 99
  • [39] Proof of Concept for an Automated Image Analysis Method to Quantify Rat Bone Marrow Hematopoietic Lineages on H&E Sections
    Kozlowski, Cleopatra
    Fullerton, Aaron
    Cain, Gary
    Katavolos, Paula
    Bravo, Joseph
    Tarrant, Jacqueline M.
    TOXICOLOGIC PATHOLOGY, 2018, 46 (03) : 336 - 347
  • [40] Human bone marrow stromal cell: Coexpression of markers specific for multiple mesenchymal cell lineages
    Seshi, B
    Kumar, S
    Sellers, D
    BLOOD CELLS MOLECULES AND DISEASES, 2000, 26 (03) : 234 - 246