Mesenchymal Stem Cells Promote Pancreatic Tumor Growth by Inducing Alternative Polarization of Macrophages

被引:98
作者
Mathew, Esha [1 ]
Brannon, Arthur L. [1 ,2 ]
Del Vecchio, AnnaChiara [3 ]
Garcia, Paloma E. [4 ]
Penny, Morgan K. [5 ]
Kane, Kevin T. [3 ]
Vinta, Alekya [3 ]
Buckanovich, Ronald J. [1 ,6 ]
di Magliano, Marina Pasca [1 ,2 ,3 ,7 ]
机构
[1] Univ Michigan, Cellular & Mol Biol Program, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Med Scientist Training Program, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Surg, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Program Pathol, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Program Canc Biol, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[7] Univ Michigan, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
来源
NEOPLASIA | 2016年 / 18卷 / 03期
关键词
CANCER PROGRESSION; STROMAL CELLS; T-CELL; FIBROBLASTS; IMMUNOTHERAPY; ACTIVATION; DEPLETION; INVASION; THERAPY; PATHWAY;
D O I
10.1016/j.neo.2016.01.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic cancer is characterized by an extensive desmoplastic stroma, the functional relevance of which is poorly understood. Activated fibroblasts are a prevalent component of the stroma, and traditionally, these cells have been considered as a homogenous population derived from pancreatic stellate cells. In this study, we highlight a previously unappreciated heterogeneity of the fibroblast population within the stroma. In particular, a subset of stromal fibroblasts has characteristics of mesenchymal stem cells (MSCs). MSCs are present in the normal pancreas as well as in the carcinomatous pancreas (CA-MSCs). Here, we determine that CA-MSCs have increased tumor-promoting function compared with MSCs in normal pancreas. This ability to promote tumor growth is associated with CA-MSCs' unique ability to promote alternative macrophage polarization. Thus, our study identifies a previously uncharacterized cell population within the stroma and sheds light on tumor-promoting interactions between different components of the stroma. Significance Targeting the stroma is emerging as a new paradigmin pancreatic cancer; however, efforts to that effect are hampered by our limited understanding of the nature and function of stromal components. Here, we uncover previously unappreciated heterogeneity within the stroma and identify interactions among stromal components that promote tumor growth and could be targeted therapeutically.
引用
收藏
页码:142 / 151
页数:10
相关论文
共 36 条
[1]   c-Myc expression and MEK1-induced Erk2 nuclear localization are required for TGF-beta induced epithelialmesenchymal transition and invasion in prostate cancer [J].
Amatangelo, Michael D. ;
Goodyear, Shaun ;
Varma, Devika ;
Stearns, Mark E. .
CARCINOGENESIS, 2012, 33 (10) :1965-1975
[2]   Desmoplastic reaction in pancreatic cancer - Role of pancreatic stellate cells [J].
Apte, MV ;
Park, S ;
Phillips, PA ;
Santucci, N ;
Goldstein, D ;
Kumar, RK ;
Ramm, GA ;
Buchler, M ;
Friess, H ;
McCarroll, JA ;
Keogh, G ;
Merrett, N ;
Pirola, R ;
Wilson, JS .
PANCREAS, 2004, 29 (03) :179-187
[3]   Mesenchymal stem cells derived from human exocrine pancreas express transcription factors implicated in beta-cell development [J].
Baertschiger, Reto M. ;
Bosco, Domenico ;
Morel, Philippe ;
Serre-Beinier, Veronique ;
Berney, Thierry ;
Buhler, Leo H. ;
Gonelle-Gispert, Carmen .
PANCREAS, 2008, 37 (01) :75-84
[4]   Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes [J].
Biankin, Andrew V. ;
Waddell, Nicola ;
Kassahn, Karin S. ;
Gingras, Marie-Claude ;
Muthuswamy, Lakshmi B. ;
Johns, Amber L. ;
Miller, David K. ;
Wilson, Peter J. ;
Patch, Ann-Marie ;
Wu, Jianmin ;
Chang, David K. ;
Cowley, Mark J. ;
Gardiner, Brooke B. ;
Song, Sarah ;
Harliwong, Ivon ;
Idrisoglu, Senel ;
Nourse, Craig ;
Nourbakhsh, Ehsan ;
Manning, Suzanne ;
Wani, Shivangi ;
Gongora, Milena ;
Pajic, Marina ;
Scarlett, Christopher J. ;
Gill, Anthony J. ;
Pinho, Andreia V. ;
Rooman, Ilse ;
Anderson, Matthew ;
Holmes, Oliver ;
Leonard, Conrad ;
Taylor, Darrin ;
Wood, Scott ;
Xu, Qinying ;
Nones, Katia ;
Fink, J. Lynn ;
Christ, Angelika ;
Bruxner, Tim ;
Cloonan, Nicole ;
Kolle, Gabriel ;
Newell, Felicity ;
Pinese, Mark ;
Mead, R. Scott ;
Humphris, Jeremy L. ;
Kaplan, Warren ;
Jones, Marc D. ;
Colvin, Emily K. ;
Nagrial, Adnan M. ;
Humphrey, Emily S. ;
Chou, Angela ;
Chin, Venessa T. ;
Chantrill, Lorraine A. .
NATURE, 2012, 491 (7424) :399-405
[5]   Mesenchymal stem cells reciprocally regulate the M1/M2 balance in mouse bone marrow-derived macrophages [J].
Cho, Dong-Im ;
Kim, Mi Ra ;
Jeong, Hye-yun ;
Jeong, Hae Chang ;
Jeong, Myung Ho ;
Yoon, Sung Ho ;
Kim, Yong Sook ;
Ahn, Youngkeun .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2014, 46 :e70-e70
[6]   Dynamics of the immune reaction to pancreatic cancer from inception to invasion [J].
Clark, Carolyn E. ;
Hingorani, Sunil R. ;
Mick, Rosemarie ;
Combs, Chelsea ;
Tuveson, David A. ;
Vonderheide, Robert H. .
CANCER RESEARCH, 2007, 67 (19) :9518-9527
[7]   Metastatic Pancreatic Cancer Is Dependent on Oncogenic Kras in Mice [J].
Collins, Meredith A. ;
Brisset, Jean-Christophe ;
Zhang, Yaqing ;
Bednar, Filip ;
Pierre, Josette ;
Heist, Kevin A. ;
Galban, Craig J. ;
Galban, Stefanie ;
di Magliano, Marina Pasca .
PLOS ONE, 2012, 7 (12)
[8]   A perivascular origin for mesenchymal stem cells in multiple human organs [J].
Crisan, Mihaela ;
Yap, Solomon ;
Casteilla, Louis ;
Chen, Chien-Wen ;
Corselli, Mirko ;
Park, Tea Soon ;
Andriolo, Gabriella ;
Sun, Bin ;
Zheng, Bo ;
Zhang, Li ;
Norotte, Cyrille ;
Teng, Pang-Ning ;
Traas, Jeremy ;
Schugar, Rebecca ;
Deasy, Bridget M. ;
Badylak, Stephen ;
Buehring, Hans-Joerg ;
Giacobino, Jean-Paul ;
Lazzari, Lorenza ;
Huard, Johnny ;
Peault, Bruno .
CELL STEM CELL, 2008, 3 (03) :301-313
[9]   Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement [J].
Dominici, M. ;
Le Blanc, K. ;
Mueller, I. ;
Slaper-Cortenbach, I. ;
Marini, F. C. ;
Krause, D. S. ;
Deans, R. J. ;
Keating, A. ;
Prockop, D. J. ;
Horwitz, E. M. .
CYTOTHERAPY, 2006, 8 (04) :315-317
[10]   Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair [J].
Duffield, JS ;
Forbes, SJ ;
Constandinou, CM ;
Clay, S ;
Partolina, M ;
Vuthoori, S ;
Wu, SJ ;
Lang, R ;
Iredale, JP .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (01) :56-65