The role of stem cells in limb regeneration

REFERENCES

• Bode HR. Head regeneration in Hydra. Dev Dyn 2003; 226:225-36; PMID:12557201; http://dx.doi.org/10.1002/dvdy.10225
   PubMed Web of Science ®Google Scholar
• Rink JC. Stem cell systems and regeneration in planaria. Dev Genes Evol 2013; 223:67-84; PMID:23138344; http://dx.doi.org/10.1007/s00427-012-0426-4
   PubMed Web of Science ®Google Scholar
• Trembley M. Observations and Experiments upon the Freshwater Polypus, by Monsieur Trembley, at the Hague. Translated from the French by PHZFRS. Philosophical Transactions 1742; 42:iii-xi; http://dx.doi.org/10.1098/rstl.1742.0005
   Google Scholar
• Dinsmore CE. Urodele limb and tail regeneration in early biological thought: an essay on scientific controversy and social change. Int J Dev Biol 1996; 40:621-7; PMID:8877433
   PubMed Web of Science ®Google Scholar
• Spallanzani L. Nouvelles Recherches, Part 1-2: Sur Les Decouvertes Microscopiques Et La Generation Des Corps Organises (1769). 2009 Apr 30; pg 680.
   Google Scholar
• Frobisch NB, Bickelmann C, Witzmann F. Early evolution of limb regeneration in tetrapods: evidence from a 300-million-year-old amphibian. Proc Biol Sci 2014; 281:20141550; PMID:25253458; http://dx.doi.org/10.1098/rspb.2014.1550
   PubMed Web of Science ®Google Scholar
• Frobisch NB, Bickelmann C, Olori JC, Witzmann F. Deep-time evolution of regeneration and preaxial polarity in tetrapod limb development. Nature 2015; 527:231-4; PMID:26503047; http://dx.doi.org/10.1038/nature15397
   PubMed Web of Science ®Google Scholar
• Larson BJ, Longaker MT, Lorenz HP. Scarless fetal wound healing: a basic science review. Plast Reconstr Surg 2010; 126:1172-80; PMID:20885241; http://dx.doi.org/10.1097/PRS.0b013e3181eae781
   PubMed Web of Science ®Google Scholar
• Yokoyama H. Initiation of limb regeneration: the critical steps for regenerative capacity. Dev Growth Differ 2008; 50:13-22; PMID:17986260; http://dx.doi.org/10.1111/j.1440-169X.2007.00973.x
   PubMed Web of Science ®Google Scholar
• Schotte OE, Smith CB. Wound healing processes in amputated mouse digits. Biol Bull 1959; 117:546-61; http://dx.doi.org/10.2307/1538866
   Web of Science ®Google Scholar
• Borgens RB. Mice regrow the tips of their foretoes. Science 1982; 217:747-50; PMID:7100922; http://dx.doi.org/10.1126/science.7100922
   PubMed Web of Science ®Google Scholar
• Han M, Yang X, Lee J, Allan CH, Muneoka K. Development and regeneration of the neonatal digit tip in mice. Dev Biol 2008; 315:125-35; PMID:18234177; http://dx.doi.org/10.1016/j.ydbio.2007.12.025
   PubMed Web of Science ®Google Scholar
• Takeo M, Chou WC, Sun Q, Lee W, Rabbani P, Loomis C, et al. Wnt activation in nail epithelium couples nail growth to digit regeneration. Nature 2013; 499:228-32; PMID:23760480; http://dx.doi.org/10.1038/nature12214
   PubMed Web of Science ®Google Scholar
• Illingworth CM. Trapped fingers and amputated finger tips in children. J Pediatr Surg 1974; 9:853-58; PMID:4473530; http://dx.doi.org/10.1016/S0022-3468(74)80220-4
   PubMed Web of Science ®Google Scholar
• Rosenthal LJ, Reiner MA, Bleicher MA. Nonoperative management of distal fingertip amputations in children. Pediatrics 1979; 64:1-3; PMID:450537
   PubMed Web of Science ®Google Scholar
• Vidal P, Dickson MG. Regeneration of the distal phalanx. A case report. J Hand Surg Br 1993; 18:230-3; PMID:8501382; http://dx.doi.org/10.1016/0266-7681(93)90116-W
   PubMedGoogle Scholar
• Tamura K, Ohgo S, Yokoyama H. Limb blastema cell: a stem cell for morphological regeneration. Dev Growth Differ 2010; 52:89-99; PMID:19891640; http://dx.doi.org/10.1111/j.1440-169X.2009.01144.x
   PubMed Web of Science ®Google Scholar
• Hyun JS, Chung MT, Wong VW, Montoro D, Longaker MT, Wan DC. Rethinking the blastema. Plast Reconstr Surg 2012; 129:1097-103; PMID:22544093; http://dx.doi.org/10.1097/PRS.0b013e31824a2c49
   PubMed Web of Science ®Google Scholar
• Tanaka EM. Cell differentiation and cell fate during urodele tail and limb regeneration. Curr Opin Genet Dev 2003; 13:497-501; PMID:14550415; http://dx.doi.org/10.1016/j.gde.2003.08.003
   PubMed Web of Science ®Google Scholar
• Simon A, Tanaka EM. Limb regeneration. Wiley Interdiscip Rev Dev Biol 2013; 2:291-300; PMID:24009038; http://dx.doi.org/10.1002/wdev.73
   PubMed Web of Science ®Google Scholar
• Iten LE, Bryant SV. Forelimb regeneration from different levels of amputation in the newt,Notophthalmus viridescens: Length, rate, and stages. Wilhelm Roux' Archiv für Entwicklungsmechanik der Organismen 1973; 173:263-82; http://dx.doi.org/10.1007/BF00575834
   Google Scholar
• Fukazawa T, Naora Y, Kunieda T, Kubo T. Suppression of the immune response potentiates tadpole tail regeneration during the refractory period. Development 2009; 136:2323-7; PMID:19515697; http://dx.doi.org/10.1242/dev.033985
   PubMed Web of Science ®Google Scholar
• Mescher AL, Neff AW, King MW. Changes in the inflammatory response to injury and its resolution during the loss of regenerative capacity in developing Xenopus limbs. PloS One 2013; 8:e80477; PMID:24278286; http://dx.doi.org/10.1371/journal.pone.0080477
   PubMedGoogle Scholar
• Godwin JW, Pinto AR, Rosenthal NA. Macrophages are required for adult salamander limb regeneration. Proc Natl Acad Sci U S A 2013; 110:9415-20; PMID:23690624; http://dx.doi.org/10.1073/pnas.1300290110
   PubMed Web of Science ®Google Scholar
• Yun MH, Davaapil H, Brockes JP. Recurrent turnover of senescent cells during regeneration of a complex structure. Elife 2015; 4; PMID:25942455; http://dx.doi.org/10.7554/eLife.05505
   PubMedGoogle Scholar
• Sousa-Victor P, Gutarra S, Garcia-Prat L, Rodriguez-Ubreva J, Ortet L, Ruiz-Bonilla V, Jardí M, Ballestar E, González S, Serrano AL, et al. Geriatric muscle stem cells switch reversible quiescence into senescence. Nature 2014; 506:316-21; PMID:24522534; http://dx.doi.org/10.1038/nature13013
   PubMed Web of Science ®Google Scholar
• Telgenhoff D, Shroot B. Cellular senescence mechanisms in chronic wound healing. Cell Death Differ 2005; 12:695-8; PMID:15861190; http://dx.doi.org/10.1038/sj.cdd.4401632
   PubMed Web of Science ®Google Scholar
• Mastellos DC, Deangelis RA, Lambris JD. Complement-triggered pathways orchestrate regenerative responses throughout phylogenesis. Semin Immunol 2013; 25:29-38; PMID:23684626; http://dx.doi.org/10.1016/j.smim.2013.04.002
   PubMed Web of Science ®Google Scholar
• Bryant SV, Endo T, Gardiner DM. Vertebrate limb regeneration and the origin of limb stem cells. Int J Dev Biol 2002; 46:887-96; PMID:12455626
   PubMed Web of Science ®Google Scholar
• Heber-Katz E, Zhang Y, Bedelbaeva K, Song F, Chen X, Stocum DL. Cell cycle regulation and regeneration. Curr Top Microbiol Immunol 2013; 367:253-76; PMID:23263201
   PubMed Web of Science ®Google Scholar
• Satoh A, Graham GM, Bryant SV, Gardiner DM. Neurotrophic regulation of epidermal dedifferentiation during wound healing and limb regeneration in the axolotl (Ambystoma mexicanum). Dev Biol 2008; 319:321-35; PMID:18533144; http://dx.doi.org/10.1016/j.ydbio.2008.04.030
   PubMed Web of Science ®Google Scholar
• Kragl M, Knapp D, Nacu E, Khattak S, Maden M, Epperlein HH, Tanaka EM. Cells keep a memory of their tissue origin during axolotl limb regeneration. Nature 2009; 460:60-5; PMID:19571878; http://dx.doi.org/10.1038/nature08152
   PubMed Web of Science ®Google Scholar
• Rinkevich Y, Lindau P, Ueno H, Longaker MT, Weissman IL. Germ-layer and lineage-restricted stem/progenitors regenerate the mouse digit tip. Nature 2011; 476:409-13; PMID:21866153; http://dx.doi.org/10.1038/nature10346
   PubMed Web of Science ®Google Scholar
• Lehoczky JA, Robert B, Tabin CJ. Mouse digit tip regeneration is mediated by fate-restricted progenitor cells. Proc Natl Acad Sci U S A 2011; 108:20609-14; PMID:22143790; http://dx.doi.org/10.1073/pnas.1118017108
   PubMed Web of Science ®Google Scholar
• Tanaka EM, Reddien PW. The cellular basis for animal regeneration. Dev Cell 2011; 21:172-85; PMID:21763617; http://dx.doi.org/10.1016/j.devcel.2011.06.016
   PubMed Web of Science ®Google Scholar
• Maden M. Neurotrophic control of the cell cycle during amphibian limb regeneration. J Embryol Exp Morphol 1978; 48:169-75; PMID:744947
   PubMedGoogle Scholar
• Smith AR, Wolpert L. Nerves and angiogenesis in amphibian limb regeneration. Nature 1975; 257:224-5; PMID:1161022; http://dx.doi.org/10.1038/257224a0
   PubMed Web of Science ®Google Scholar
• Stocum DL. The role of peripheral nerves in urodele limb regeneration. Eur J Neurosci 2011; 34:908-16; PMID:21929624; http://dx.doi.org/10.1111/j.1460-9568.2011.07827.x
   PubMed Web of Science ®Google Scholar
• Satoh A, Gardiner DM, Bryant SV, Endo T. Nerve-induced ectopic limb blastemas in the Axolotl are equivalent to amputation-induced blastemas. Dev Biol 2007; 312:231-44; PMID:17959163; http://dx.doi.org/10.1016/j.ydbio.2007.09.021
   PubMed Web of Science ®Google Scholar
• Kumar A, Delgado JP, Gates PB, Neville G, Forge A, Brockes JP. The aneurogenic limb identifies developmental cell interactions underlying vertebrate limb regeneration. Proc Natl Acad Sci U S A 2011; 108:13588-93; PMID:21825124; http://dx.doi.org/10.1073/pnas.1108472108
   PubMed Web of Science ®Google Scholar
• Kumar A, Godwin JW, Gates PB, Garza-Garcia AA, Brockes JP. Molecular basis for the nerve dependence of limb regeneration in an adult vertebrate. Science 2007; 318:772-7; PMID:17975060; http://dx.doi.org/10.1126/science.1147710
   PubMed Web of Science ®Google Scholar
• Mohammad KS, Neufeld DA. Denervation retards but does not prevent toetip regeneration. Wound Repair Regen 2000; 8(4):277-81; PMID: 11013019
   Google Scholar
• Rinkevich Y, Montoro DT, Muhonen E, Walmsley GG, Lo D, Hasegawa M, Januszyk M, Connolly AJ, Weissman IL, Longaker MT. Clonal analysis reveals nerve-dependent and independent roles on mammalian hind limb tissue maintenance and regeneration. Proc Natl Acad Sci U S A 2014; 111:9846-51; PMID:24958860; http://dx.doi.org/10.1073/pnas.1410097111
   PubMed Web of Science ®Google Scholar
• Gardiner DM, Muneoka K, Bryant SV. The migration of dermal cells during blastema formation in axolotls. Dev Biol 1986; 118:488-93; PMID:379-2618; http://dx.doi.org/10.1016/0012-1606(86)900-20-5
   PubMedGoogle Scholar
• Muneoka K, Fox WF, Bryant SV. Cellular contribution from dermis and cartilage to the regenerating limb blastema in axolotls. Dev Biol 1986; 116:256-60; PMID:3732605; http://dx.doi.org/10.1016/0012-1606(86)90062-X
   PubMed Web of Science ®Google Scholar
• Hirata A, Gardiner DM, Satoh A. Dermal fibroblasts contribute to multiple tissues in the accessory limb model. Dev Growth Differ 2010; 52:343-50; PMID:20148925; http://dx.doi.org/10.1111/j.1440-169X.2009.01165.x
   PubMed Web of Science ®Google Scholar
• Satoh A, Bryant SV, Gardiner DM. Regulation of dermal fibroblast dedifferentiation and redifferentiation during wound healing and limb regeneration in the Axolotl. Dev Growth Differ 2008; 50:743-54; PMID:19046162; http://dx.doi.org/10.1111/j.1440-169X.2008.01072.x
   PubMed Web of Science ®Google Scholar
• Egawa S, Miura S, Yokoyama H, Endo T, Tamura K. Growth and differentiation of a long bone in limb development, repair and regeneration. Dev Growth Differ 2014; 56:410-24; PMID:24860986; http://dx.doi.org/10.1111/dgd.12136
   PubMed Web of Science ®Google Scholar
• Said S, Parke W, Neufeld DA. Vascular supplies differ in regenerating and nonregenerating amputated rodent digits. Anat Rec A Discov Mole Cell Evol Biol 2004; 278:443-9; PMID:15103739; http://dx.doi.org/10.1002/ar.a.20034
   PubMedGoogle Scholar
• Sousa S, Afonso N, Bensimon-Brito A, Fonseca M, Simoes M, Leon J, Roehl H, Cancela ML, Jacinto A. Differentiated skeletal cells contribute to blastema formation during zebrafish fin regeneration. Development 2011; 138:3897-905; PMID:21862555; http://dx.doi.org/10.1242/dev.064717
   PubMed Web of Science ®Google Scholar
• Watson CJ, Kwon RY. Osteogenic programs during zebrafish fin regeneration. Bonekey Rep 2015; 4:745; PMID:26421148; http://dx.doi.org/10.1038/bonekey.2015.114
   PubMedGoogle Scholar
• Wehner D, Weidinger G. Signaling networks organizing regenerative growth of the zebrafish fin. Trends Genet 2015; 31:336-43; PMID:25929514; http://dx.doi.org/10.1016/j.tig.2015.03.012
   PubMed Web of Science ®Google Scholar
• Duran I, Ruiz-Sanchez J, Santamaria JA, Mari-Beffa M. Holmgren's principle of delamination during fin skeletogenesis. Mech Dev 2015; 135:16-30; PMID:25460362; http://dx.doi.org/10.1016/j.mod.2014.11.002
   PubMed Web of Science ®Google Scholar
• Oustanina S, Hause G, Braun T. Pax7 directs postnatal renewal and propagation of myogenic satellite cells but not their specification. EMBO J 2004; 23:3430-9; PMID:15282552; http://dx.doi.org/10.1038/sj.emboj.7600346
   PubMed Web of Science ®Google Scholar
• von Maltzahn J, Jones AE, Parks RJ, Rudnicki MA. Pax7 is critical for the normal function of satellite cells in adult skeletal muscle. Proc Natl Acad Sci U S A 2013; 110:16474-9; PMID:24065826; http://dx.doi.org/10.1073/pnas.1307680110
   PubMed Web of Science ®Google Scholar
• Relaix F, Zammit PS. Satellite cells are essential for skeletal muscle regeneration: the cell on the edge returns centre stage. Development 2012; 139:2845-56; PMID:22833472; http://dx.doi.org/10.1242/dev.069088
   PubMed Web of Science ®Google Scholar
• Morrison JI, Borg P, Simon A. Plasticity and recovery of skeletal muscle satellite cells during limb regeneration. FASEB J 2010; 24:750-6; PMID:19887652; http://dx.doi.org/10.1096/fj.09-134825
   PubMed Web of Science ®Google Scholar
• Sandoval-Guzman T, Wang H, Khattak S, Schuez M, Roensch K, Nacu E, Tazaki A, Joven A, Tanaka EM, Simon A. Fundamental differences in dedifferentiation and stem cell recruitment during skeletal muscle regeneration in two salamander species. Cell stem Cell 2014; 14:174-87; PMID:24268695; http://dx.doi.org/10.1016/j.stem.2013.11.007
   PubMed Web of Science ®Google Scholar
• McCusker CD, Gardiner DM. Positional information is reprogrammed in blastema cells of the regenerating limb of the axolotl (Ambystoma mexicanum). PloS One 2013; 8:e77064; PMID:24086768; http://dx.doi.org/10.1371/journal.pone.0077064
   PubMedGoogle Scholar
• Stocum DL, Melton DA. Self-organizational capacity of distally transplanted limb regeneration blastemas in larval salamanders. J Exp Zool 1977; 201:451-61; PMID:908916; http://dx.doi.org/10.1002/jez.1402010312
   PubMedGoogle Scholar
• Echeverri K, Tanaka EM. Proximodistal patterning during limb regeneration. Dev Biol 2005; 279:391-401; PMID:15733667; http://dx.doi.org/10.1016/j.ydbio.2004.12.029
   PubMed Web of Science ®Google Scholar
• Gardiner DM, Blumberg B, Komine Y, Bryant SV. Regulation of HoxA expression in developing and regenerating axolotl limbs. Development 1995; 121:1731-41; PMID:7600989
   PubMed Web of Science ®Google Scholar
• McCusker CD, Gardiner DM. Understanding positional cues in salamander limb regeneration: implications for optimizing cell-based regenerative therapies. Dis Model Mech 2014; 7:593-9; PMID:24872456; http://dx.doi.org/10.1242/dmm.013359
   PubMed Web of Science ®Google Scholar
• Monaghan JR, Maden M. Visualization of retinoic acid signaling in transgenic axolotls during limb development and regeneration. Dev Biol 2012; 368:63-75; PMID:22627291; http://dx.doi.org/10.1016/j.ydbio.2012.05.015
   PubMed Web of Science ®Google Scholar
• Echeverri K, Tanaka EM. Ectoderm to mesoderm lineage switching during axolotl tail regeneration. Science 2002; 298:1993-6; PMID:12471259; http://dx.doi.org/10.1126/science.1077804
   PubMed Web of Science ®Google Scholar
• Walmsley GG, Hu MS, Hong WX, Maan ZN, Lorenz HP, Longaker MT. A mouse fetal skin model of scarless wound repair. J Vis Exp 2015; 95:52297; PMID:25650841; http://dx.doi.org/10.3791/52297
   PubMed Web of Science ®Google Scholar
• Denis JF, Levesque M, Tran SD, Camarda AJ, Roy S. Axolotl as a Model to Study Scarless Wound Healing in Vertebrates: Role of the Transforming Growth Factor Beta Signaling Pathway. Adv Wound Care 2013; 2:250-60; PMID:24527347; http://dx.doi.org/10.1089/wound.2012.0371
   PubMedGoogle Scholar
• Rinkevich Y, Walmsley GG, Hu MS, Maan ZN, Newman AM, Drukker M, Januszyk M, Krampitz GW, Gurtner GC, Lorenz HP, et al. Skin fibrosis. Identification and isolation of a dermal lineage with intrinsic fibrogenic potential. Science 2015; 348:aaa2151; PMID:25883361; http://dx.doi.org/10.1126/science.aaa2151
   PubMed Web of Science ®Google Scholar
• Satoh A, Hirata A, Makanae A. Collagen reconstitution is inversely correlated with induction of limb regeneration in Ambystoma mexicanum. Zoolog Sci 2012; 29:191-7; PMID:22379987; http://dx.doi.org/10.2108/zsj.29.191
   PubMed Web of Science ®Google Scholar