Immunocalization of telomerase in cells of lizard tail after amputation suggests cell activation for tail regeneration

Tissue and Cell

Volumn 48, Issue 1, 2016, Pages 63-71

  Alibardi, L ^a  

^a UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

Amputation; Immunocytochemistry; Lizard; Regeneration; Tail; Telomerase

Indexed keywords

TELOMERASE;

ADIPOCYTE; ANIMAL TISSUE; ANOLIS CAROLINENSIS; ARTICLE; AUTOTOMY; BASOPHIL; BLASTEMA; CELL ACTIVATION; CELL NUCLEUS; CELL PROLIFERATION; CONTROLLED STUDY; ENZYME ACTIVATION; ERYTHROBLAST; FIBROBLAST; IMMUNOLOCALIZATION; LIZARD; LYMPHOBLAST; NONHUMAN; PODARCIS MURALIS; SKELETAL MUSCLE SATELLITE CELL; TAIL; TISSUE REGENERATION; AMPUTATION; ANIMAL; EPIDERMIS; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; REGENERATION;

AMPUTATION; ANIMALS; CELL PROLIFERATION; EPIDERMIS; FIBROBLASTS; LIZARDS; REGENERATION; TAIL; TELOMERASE;

EID: 84950261557     PISSN: 00408166     EISSN: 15323072     Source Type: Journal    
DOI: 10.1016/j.tice.2015.10.004     Document Type: Article

References (35)

1. Alibardi, L., Production of immature erythrocytes in lizard during tail regeneration. Anim. Biol. 3 (1994), 139–147.
2. Alibardi, L., Morphological and cellular aspects of tail and limb regeneration in lizard: a model system with implications for tissue regeneration in mammals. Adv. Anat. Embryol. Cell. Biol. 207 (2010), 1–112.
3. Alibardi, L., Ultrastructural features of the process of wound healing after tail and limb amputation in lizard. Acta Zool. 91 (2010), 306–318.
4. Alibardi, L., Histochemical biochemical and cell biological aspects of tail regeneration in lizard, an amniote model for studies on tissue regeneration. Progr. Histoch. Cytoch. 48 (2014), 143–244.
5. Alibardi, L., Immunolocalization of the telomerase-1 component in cells of the regenerating tail, testis, and intestine of lizards. J. Morphol., 2015, 10.1002/jmor.20375.
6. Alibardi, L., Immunolocalization of a p53/p63-like protein in the regenerating tail epidermis of the wall lizard (Podarcis muralis) suggests it is involved in the differentiation of the epidermis. Acta Zool., 2015, 10.1111/azo.12130.
7. Alibardi, L., Immunolocalization indicates that both original and regenerated lizard tail tissues contain populations of long retaining cells, putative stem/progenitor cells. Microsc. Res. Techn., 2015.
8. Alibardi, L., Immunodetection of Telomerase-like immunoreactivity in normal and regenerating tail of amphibians suggests it is related to their regenerative capacity. J. Exp. Zool. A, 2015.
9. Alibardi, L., Sala, M., Fine structure of the blastema in the regenerating tail of the lizard Podarcis sicula. Boll. Zool. 55 (1988), 307–313.
10. Alibardi, L., Toni, M., Wound keratins in the regenerating epidermis of lizard suggest that the wound reaction is similar in the tail and limb. J. Exp. Zool. 303A (2005), 845–860.
11. Bellairs, A.A., d'Bryant, S.V., Autotomy and regeneration in reptiles. Gans, C., Billet, F., Maderson, P.F.A., (eds.) Biology of the Reptilia, vol. 15B, 1985, John Wiley& Sons, NY, USA, 302–410.
12. Broccoli, D., Young, J.W., de Lange, T., Telomerase activity in normal and malignant hematopoietic cells. PNAS 92 (1995), 9082–9086.
13. Cox, P.G., Some aspects of tail regeneration in the lizard Anolis carolinensis. I. A description based on histology and autoradiography. J. Exp. Zool. 171 (1969), 127–150.
14. Counter, C.M., Gupta, J., Harley, C.B., Leber, B., Bacchetti, S., Telomerase activity in normal leucocytes and in Hematological malignancies. Blood 85 (1995), 2315–2320.
15. Dell'Aica, I., Rossini, K., Sandri, M., Destro, C., Carraro, U., Telomerase activity in regenerated normal muscles: effects of repeated injuries. Basic Appl. Myol. 12 (2002), 73–76.
16. Delorme, S.L., Lungu, I.M., Vickaryous, M.K., Scar-free wound healing and regeneration following tail loss in the leopard gecko Eublepharis macularius. Anat. Rec. 295 (2012), 1575–1595.
17. Elmore, L.W., Norris, M.W., Sircar, S., Taylor-Bright, A., McChesney, P.A., Winn, R.N., Holt, S.E., Upregulation of telomerase function during tissue regeneration. Exper. Biol. Med. 233 (2008), 958–967.
18. Fisher, R.E., Geiger, L.A., Stroik, L.K., Hutchins, E.D., George, R.M., DeNardo, D.F., Kosumi, K., Rawls, J.A., Wilson-Rawls, J., A histological comparison of the original and regenerated tail in the green anole Anolis carolinensis. Anat. Rec. 295 (2012), 1609–1619.
19. Flanary, B.E., Streit, W.J., Effects of axotomy on telomere length, telomerase activity, and protein in activated microglia. J. Neurosci. 82 (2005), 160–171.
20. Gilbert, E.A.B., Payne, S.L., Vickaryous, M.K., The anatomy and histology of caudal autotomy and regeneration in lizards. Physiol. Bioch. Zool. 86 (2013), 631–644.
21. Hutchins, E.D., Markov, G.J., Eckalbar, W.L., Gorge, R.M., King, J.M., Tokuyama, M.A., Geiger, L.A., Emmert, N., Ammar, M.J., Allen, A.P., Siniard, A.L., Corneveaux, J.J., Fisher, R.E., Wade, J., DeNardo, D.F., Rawls, J.A., Huentelman, M.J., Wilson-Rawls, J., Kosumi, K., Transcriptomic analysis of tail regeneration in the lizard Anolis carolinensis reveals activation of conserved vertebrate developmental and repair mechanisms. Plos One, 9, 2014, e105004.
22. Kang, H.J., Choi, Y.S., Hong, S.B., Kim, K.W., Woo, R.S., Won, S.J., Kim, E.J., Jeon, H.K., Jo, S.Y., Kim, T.K., Bachoo, R., Reynold, I.J., Gwag, B.J., Lee, H.W., Ectopic expression of the catalytic subunit of telomerase protects against brain injury resulting from ischemia and NMDA-induced neurotoxicity. J. Neurosci. 24 (2004), 1280–1287.
23. Lozito, T.P., Tuan, R.S., Lizard tail regeneration: regulation of two distinct cartilage regions by Indian hedgehog. Dev. Biol., 2015 doi:org/10.1016/j.ydbio.2014.12.036i.
24. Lund, T.C., Glass, T.J., Tolar, J., Blazar, B.R., Expression of telomerase and telomere length are unaffected by either age or limb regeneration in Danio rerio. PLOS One, 4, 2009, e7688.
25. McLean, C.E., Vickaryous, M.K., A novel amniote model of epimorphic regeneration: the leopard gecko Eublepharis macularius. BMC Dev. Biol. 11 (2011), 50–74.
26. Nozaki, Y., Liu, T., Hatano, K., Gharaee-Kermani, M., Phan, S.H., Induction of telomerase activity in fribroblasts from bleomycin-injured lungs. Am. J. Respir. Cell Mol. Biol. 23 (2000), 460–465.
27. Quattrini, D., Piano di autotomia e rigenerazione della coda nei Sauri. Arch. Ital. Anat. Embriol. 59 (1954), 225–282.
28. Park, J.I.I., Venteicher, A.S., Hong, J.Y., Choi, J., Jun, S., Shkreli, M., Chang, W., Meng, Z., Cheung, P., Ji, H., McLaughlin, M., Veenstra, T.D., Nusse, R., McCrea, P.D., Artandi, S.E., Telomerase modulates Wnt signaling by association with target gene chromatin. Nature 460 (2009), 66–73.
29. Sarin, K.Y., Cheung, P., Gilison, D., Lee, E., Tennen, R.I., Wang, E., Artandi, M.K., Oro, A.E., Artandi, S.E., CVonditional telomerase induction causes proliferation of follicle stem cells. Nature 18 (2005), 1048–1052.
30. Scala, C., Cenacchi, G., Ferrari, C., Pasquinelli, G., Preda, P., Manara, G.C., A new acrylic resin formulation: a useful tool for histological, ultrastructural, and immunocytochemical investigations. J. Histochem. Cytochem. 40 (1992), 1799–1804.
31. Shah, R.V., Kinariwala, R.V., Ramachandran, A.V., Haematopoiesis and regeneration: changes in the cellular elements of blood and haemoglobin during tail regeneration in the scincid lizard Mabuya carinata. Mon. Zool. Ital. N.S. 14 (1980), 137–150.
32. Simpson, S.B., Kiortsis, V., Trampusch, H.A.L., (eds.) Regeneration of the Lizard Tail. Regeneration in Animals and Related Problems, 1965, Amsterdam, North-Holland, 431–443.
33. Taylor, R.S., Ramirez, R.D., Ogoshi, M., Chaffins, M., Piatyszek, M.A., Shay, J.W., Detection of telomerase activity in malignant and non-malignant skin conditions. J. Inv. Dermatol. 106 (1996), 759–765.
34. Weng, N.P., Palmer, L.D., Levine, B.L., Lane, H.C., June, C.H., Hodes, R.J., Tales of tails: regulation of telomere length and telomerase activity during lymphocyte development, differentiation, activation and aging. Immunol. Rev. 160 (1997), 43–54.
35. Werner, Y.L., Regeneration of the caudal axial skeleton in a gekkonid lizard (Hemidactylus) with particular reference to the “latent” period. Acta Zool. 48 (1967), 103–125.