Immunity in salamander regeneration: Where are we standing and where are we headed?

被引:24
作者
Bolanos-Castro, Lizbeth Airais [1 ]
Walters, Hannah Elisabeth [1 ]
Garcia Vazquez, Ruben Octavio [2 ]
Yun, Maximina Hee [1 ,3 ]
机构
[1] Tech Univ Dresden, CRTD Ctr Regenerat Therapies, Dresden, Germany
[2] Univ Florida, Coll Med, Dept Mol Genet & Microbiol, Gainesville, FL USA
[3] Max Planck Inst Mol Cell Biol & Genet, Dresden, Germany
基金
美国国家卫生研究院;
关键词
axolotl; clodronate; complement; lymphocyte; macrophage; neutrophil; newt; LIMB REGENERATION; LENS REGENERATION; MEXICAN AXOLOTL; WOUND REPAIR; NEWT LIMB; TISSUE; EXPRESSION; MACROPHAGES; CELLS; INFLAMMATION;
D O I
10.1002/dvdy.251
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Salamanders exhibit the most extensive regenerative repertoire among vertebrates, being able to accomplish scar-free healing and faithful regeneration of significant parts of the eye, heart, brain, spinal cord, jaws and gills, as well as entire appendages throughout life. The cellular and molecular mechanisms underlying salamander regeneration are currently under extensive examination, with the hope of identifying the key drivers in each context, understanding interspecies differences in regenerative capacity, and harnessing this knowledge in therapeutic settings. The immune system has recently emerged as a potentially critical player in regenerative responses. Components of both innate and adaptive immunity have been found at critical stages of regeneration in a range of salamander tissues. Moreover, functional studies have identified a requirement for macrophages during heart and limb regeneration. However, our knowledge of salamander immunity remains scarce, and a thorough definition of the precise roles played by its members is lacking. Here, we examine the evidence supporting roles for immunity in various salamander regeneration models. We pinpoint observations that need revisiting through modern genetic approaches, uncover knowledge gaps, and highlight insights from various model organisms that could guide future explorations toward an understanding of the functions of immunity in regeneration.
引用
收藏
页码:753 / 767
页数:15
相关论文
共 106 条
[11]   Live Imaging of Axolotl digit Regeneration reveals Spatiotemporal Choreography of Diverse Connective Tissue Progenitor Pools [J].
Currie, Joshua D. ;
Kawaguchi, Akane ;
Traspas, Ricardo Moreno ;
Schuez, Maritta ;
Chara, Osvaldo ;
Tanaka, Elly M. .
DEVELOPMENTAL CELL, 2016, 39 (04) :411-423
[12]   ULTRASTRUCTURE OF THE BONE-MARROW OF THE SALAMANDER PLETHODON-GLUTINOSUS (CAUDATA PLETHODONTIDAE) [J].
CURTIS, SK ;
COWDEN, RR ;
NAGEL, JW .
JOURNAL OF MORPHOLOGY, 1979, 159 (02) :151-183
[13]   The use of leukocyte profiles to measure stress in vertebrates: a review for ecologists [J].
Davis, A. K. ;
Maney, D. L. ;
Maerz, J. C. .
FUNCTIONAL ECOLOGY, 2008, 22 (05) :760-772
[14]   C1 inhibitor, a multi-functional serine protease inhibitor [J].
Davis, Alvin E., III ;
Lu, Fengxin ;
Mejia, Pedro .
THROMBOSIS AND HAEMOSTASIS, 2010, 104 (05) :886-893
[15]  
Del Rio-Tsonis K, 1998, J IMMUNOL, V161, P6819
[16]   Accelerated wound closure in neutrophil-depleted mice [J].
Dovi, JV ;
He, LK ;
DiPietro, LA .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 73 (04) :448-455
[17]   RAG expression is restricted to the first year of life in the Mexican axolotl [J].
Durand, C ;
Charlemagne, J ;
Fellah, JS .
IMMUNOGENETICS, 2000, 51 (8-9) :681-687
[18]   Wound repair and regeneration: Mechanisms, signaling, and translation [J].
Eming, Sabine A. ;
Martin, Paul ;
Tomic-Canic, Marjana .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (265)
[19]   Regulation of macrophage cytokine production by phagocytosis of apoptotic and post-apoptotic cells [J].
Fadok, VA ;
McDonald, PP ;
Bratton, DL ;
Henson, PM .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1998, 26 (04) :653-656
[20]  
Fahmy GH, 2002, IN VIVO, V16, P179