Hidden Treasures in Stem Cells of Indeterminately Growing Bilaterian Invertebrates

Stem Cell Reviews and Reports

Volumn 8, Issue 2, 2012, Pages 305-317

  Vogt, Günter ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

Adult stem cells; Ageing; Bivalvia; Cancer; Decapoda; Echinodermata; Indeterminate growth; Regeneration; Regulation; Stem cell niche

Indexed keywords

ADULT STEM CELL; ANIMAL; ANTIBODY SPECIFICITY; ARTICLE; CYTOLOGY; GROWTH, DEVELOPMENT AND AGING; INVERTEBRATE; PHYSIOLOGY; PRENATAL DEVELOPMENT; REGENERATION; STEM CELL; STEM CELL RESEARCH;

ADULT STEM CELLS; ANIMALS; INVERTEBRATES; ORGAN SPECIFICITY; REGENERATION; STEM CELL RESEARCH; STEM CELLS;

ANIMALIA; BILATERIA; BIVALVIA; CRUSTACEA; DECAPODA (CRUSTACEA); ECHINODERMATA; HEXAPODA; INVERTEBRATA; MAMMALIA; MOLLUSCA;

EID: 84861688856     PISSN: 15508943     EISSN: 15586804     Source Type: Journal    
DOI: 10.1007/s12015-011-9303-1     Document Type: Article

References (117)

1. Lanza, R., Blau, H., Melton, D., Moore, M., Thomas, E. D., Verfaillie, C., et al. (Eds.). (2004). Handbook of stem cells. Vol. 2: Adult and fetal stem cells. Amsterdam: Academic Press.
2. Robert, J. S. (2004). Model systems in stem cell biology. BioEssays, 26, 1005-1012.
3. Yi, M.-S., Hong, N., Li, Z.-D., Yan, Y., Wang, D.-K., Zhao, H.-B., et al. (2010). Medaka fish stem cells and their applications. Science China Life Sciences, 53, 426-434.
4. Müller, B., & Grossniklaus, U. (2010). Model organisms - a historical perspective. Journal of Proteomics, 73, 2054-2063.
5. Bosch, T. C. G. (Ed.). (2008). Stem cells: From Hydra to man. Heidelberg: Springer.
6. Rinkevich, B., & Matranga, V. (Eds.). (2009). Stem cells in marine organisms. Heidelberg: Springer.
7. Müller, W. E. G. (2006). The stem cell concept in sponges (Porifera): metazoan traits. Seminars in Cell & Developmental Biology, 17, 481-491.
8. Funayama, N. (2010). The stem cell system in demosponges: insights into the origin of somatic stem cells. Development, Growth & Differentiation, 52, 1-14.
9. Bosch, T. C. G., Anton-Erxleben, F., Hemmrich, G., & Khalturin, K. (2010). The Hydra polyp: nothing but an active stem cell community. Development, Growth & Differentiation, 52, 15-25.
10. Watanabe, H., Hoang, V. T., Mättner, R., & Holstein, T. W. (2009). Immortality and the base of multicellular life: lessons from cnidarian stem cells. Seminars in Cell & Developmental Biology, 20, 1114-1125.
11. Handberg-Thorsager, M., Fernandez, E., & Salo, E. (2008). Stem cells and regeneration in planarians. Frontiers in Bioscience, 13, 6374-6394.
12. Gentile, L., Cebrià, F., & Bartscherer, K. (2011). The planarian flatworm: an in vivo model for stem cell biology and nervous system regeneration. Disease Models & Mechanisms, 4, 12-19.
13. Pellettieri, J., Fitzgerald, P., Watanabe, S., Mancuso, J., Green, D. R., & Sánchez Alvarado, A. (2010). Cell death and tissue remodeling in planarian regeneration. Developmental Biology, 338, 76-85.
14. Bely, A. E., & Sikes, J. M. (2010). Acoel and platyhelminth models for stem-cell research. Journal of Biology, 9, 14.
15. Harrison, S. M. W., & Harrison, D. A. (2006). Contrasting mechanisms of stem cell maintenance in Drosophila. Seminars in Cell & Developmental Biology, 17, 518-533.
16. Ohlstein, B., & Spadling, A. (2006). The adult Drosophila posterior midgut is maintained by pluripotent stem cells. Nature, 439, 470-474.
17. Kirilly, D., & Xie, T. (2007). The Drosophila ovary: an active stem cell community. Cell Research, 17, 15-25.
18. Pearson, J., López-Onieva, L., Rojas-Ríos, P., & González-Reyes, A. (2009). Recent advances in Drosophila stem cell biology. International Journal of Developmental Biology, 53, 1329-1339.
19. Kimble, J., & Crittenden, S. L. (2007). Controls of germline stem cells, entry into meiosis, and the sperm/oocyte decision in Caenorhabditis elegans. Annual Review of Cell and Developmental Biology, 23, 405-433.
20. Cinquin, O. (2009). Purpose and regulation of stem cells: a systems-biology view from the Caenorhabditis elegans germ line. Journal of Pathology, 217, 186-198.
21. Tiozzo, S., Brown, F. D., & De Tomaso, A. W. (2008). Regeneration and stem cells in ascidians. In T. C. G. Bosch (Ed.), Stem cells: From Hydra to man (pp. 95-112). Heidelberg: Springer.
22. Rinkevich, B. (2002). The colonial urochordate Botryllus schlosseri: from stem cells and natural tissue transplantation to issues in evolutionary ecology. Bioessays, 24, 730-740.
23. Wagner, D. E., Wang, I. E., & Reddien, P. W. (2011). Clonogenic neoblasts are pluripotent adult stem cells that underlie planarian regeneration. Science, 332, 811-816.
24. Kipreos, E. T. (2005). C. elegans cell cycles: invariance and stem cell divisions. Nature Reviews Molecular Cell Biology, 6, 766-776.
25. Wills, A. A., Holdway, J. E., Major, R. J., & Poss, K. D. (2008). Regulated addition of new myocardial and epicardial cells fosters homeostatic cardiac growth and maintenance in adult zebrafish. Development, 135, 183-192.
26. Smart, N., Bollini, S., Dube, K. N., Vieira, J. M., Zhou, B., Davidson, S., et al. (2011). De novo cardiomyocytes from within the activated adult heart after injury. Nature, in press, doi: 10. 1038/nature10188.
27. Li, L., & Clevers, H. (2010). Coexistence of quiescent and active adult stem cells in mammals. Science, 327, 542-545.
28. Vogt, G. (2010). Suitability of the clonal marbled crayfish for biogerontological research: a review and perspective, with remarks on some further crustaceans. Biogerontology, 11, 643-669.
29. Vogt, G. (1994). Life-cycle and functional cytology of the hepatopancreatic cells of Astacus astacus (Crustacea, Decapoda). Zoomorphology, 114, 83-101.
30. Söderhäll, I., Bangyeekhun, E., Mayo, S., & Söderhäll, K. (2003). Hemocyte production and maturation in an invertebrate animal; proliferation and gene expression in hematopoietic stem cells of Pacifastacus leniusculus. Developmental and Comparative Immunology, 27, 661-672.
31. Song, C.-K., Johnstone, L. M., Schmidt, M., Derby, C. D., & Edwards, D. H. (2007). Social domination increases neuronal survival in the brain of juvenile crayfish Procambarus clarkii. Journal of Experimental Biology, 210, 1311-1324.
32. Candia-Carnevali, M. D., Thorndyke, M. C., & Matranga, V. (2009). Regenerating echinoderms: A promise to understand stem cells potential. In B. Rinkevich & V. Matranga (Eds.), Stem cells in marine organisms (pp. 165-186). Heidelberg: Springer.
33. Fang, Z., Feng, Q., Chi, Y., Xie, L., & Zhang, R. (2008). Investigation of cell proliferation and differentiation in the mantle of Pinctada fucata (Bivalve, Mollusca). Marine Biology, 153, 745-754.
34. Sebens, K. P. (1987). The ecology of indeterminate growth in animals. Annual Review of Ecology, Evolution, and Systematics, 18, 371-407.
35. FAO. (2010). The state of world fisheries and aquaculture 2010. Rome: Food and Agriculture Organization of the United Nations.
36. Vogt, G. (2011). Ageing and longevity in the Decapoda (Crustacea): a review. Zoologischer Anzeiger, in press, doi: 10. 1016/j. jcz. 2011. 05. 003.
37. Schöne, B. R., Fiebig, J., Pfeiffer, M., Gleß, R., Hickson, J., Johnson, A. L. A., et al. (2005). Climate records from a bivalved Methuselah (Arctica islandica, Mollusca; Iceland). Palaeogeography, Palaeoclimatology, Palaeoecology, 228, 130-148.
38. Ebert, T. A. (2008). Longevity and lack of senescence in the red sea urchin Strongylocentrotus franciscanus. Experimental Gerontology, 43, 734-738.
39. Strahl, J., & Abele, D. (2010). Cell turnover in tissues of the long-lived ocean quahog Arctica islandica and the short-lived scallop Aequipecten opercularis. Marine Biology, 157, 1283-1292.
40. Philipp, E. E. R., & Abele, D. (2008). Masters of longevity: lessons from long-lived bivalves - a mini review. Gerontology, 56, 55-65.
41. Finch, C. E. (1990). Longevity, senescence and the genome. Chicago: University of Chicago Press.
42. Vogt, G. (2008). How to minimize formation and growth of tumours: potential benefits of decapod crustaceans for cancer research. International Journal of Cancer, 123, 2727-2734.
43. Robert, J. (2010). Comparative study of tumorigenesis and tumor immunity in invertebrates and nonmammalian vertebrates. Developmental and Comparative Immunology, 34, 915-925.
44. Barber, B. J. (2004). Neoplastic diseases of commercially important marine bivalves. Aquatic Living Resources, 17, 449-466.
45. Zhang, G., Guo, X., Li, L., Xu, F., Wang, X., Qi, H., et al. (2011). The oyster genome project: an update. Plant & Animal Genomes XIX Conference, San Diego, CA, January 15-19, 2011. Abstract W038.
46. Sea Urchin Genome Sequencing Consortium. (2006). The genome of the sea urchin Strongylocentrotus purpuratus. Science, 314, 941-952.
47. Xiang, J., Zhang, X., Zhang, T., Zhao, C., Zhang, B., Liu, C., et al. (2011). Progress on genome sequencing of Pacific white shrimp Litopenaeus vannamei. Plant & Animal Genomes XIX Conference, San Diego, CA, January 15-19, 2011. Abstract P644.
48. Vogt, G. (2008). The marbled crayfish: a new model organism for research on development, epigenetics and evolutionary biology. Journal of Zoology, 276, 1-13.
49. Vogt, G. (2011). Marmorkrebs: natural crayfish clone as emerging model for various biological disciplines. Journal of Biosciences, 36, 377-382.
50. Biffis, C., Alwes, F., & Scholtz, G. (2009). Cleavage and gastrulation of the dendrobranchiate shrimp Penaeus monodon (Crustacea, Malacostraca, Decapoda). Arthropod Structure & Development, 38, 527-540.
51. Hertzler, P. L. (2002). Development of the mesendoderm in the dendrobranchiate shrimp Sicyonia ingentis. Arthropod Structure & Development, 31, 33-49.
52. Alwes, F., & Scholtz, G. (2006). Stages and other aspects of the embryology of the parthenogenetic Marmorkrebs (Decapoda, Reptantia, Astacida). Development, Genes and Evolution, 216, 169-184.
53. Harzsch, S. (2001). Neurogenesis in the crustacean ventral nerve cord: homology of neuronal stem cells in Malacostraca and Branchiopoda? Evolution & Development, 3, 154-169.
54. Krol, R. M., Hawkins, W. E., & Overstreet, R. M. (1992). Reproductive components. In F. W. Harrison & A. G. Humes (Eds.), Microscopic anatomy of invertebrates. Vol. 10: Decapod Crustacea (pp. 295-343). New York: Wiley-Liss.
55. Hinsch, G. W. (1993). Ultrastructure of spermatogonia, spermatocytes, and Sertoli cells in the testis of the crayfish, Procambarus paeninsulanus. Tissue & Cell, 25, 737-742.
56. Vogt, G., Tolley, L., & Scholtz, G. (2004). Life stages and reproductive components of the Marmorkrebs (marbled crayfish), the first parthenogenetic decapod crustacean. Journal of Morphology, 261, 286-311.
57. Zhang, Y., Allodi, S., Sandeman, D. C., & Beltz, B. S. (2010). Adult neurogenesis in the crayfish brain: proliferation, migration, and possible origin of precursor cells. Developmental Neurobiology, 69, 415-436.
58. Martynova, M. G. (1993). Satellite cells in the crayfish heart muscle functions as stem cells and are characterized by molt-dependent behaviour. Zoologischer Anzeiger, 230, 181-190.
59. Martynova, M. G. (2004). Proliferation and differentiation processes in the heart muscle elements in different phylogenetic groups. International Review of Cytology, 235, 215-250.
60. Uhrík, B., Rýdlová, K., & Zacharová, D. (1989). The roles of haemocytes during degeneration and regeneration of crayfish muscle fibres. Cell and Tissue Research, 255, 443-449.
61. Vogt, G. (2002). Functional anatomy. In D. M. Holdich (Ed.), Biology of freshwater crayfish (pp. 53-151). Oxford: Blackwell Science.
62. Zeng, H., Ye, H., Li, S., Wang, G., & Huang, J. (2010). Hepatopancreas cell cultures from mud crab, Scylla paramamosain. In Vitro Cellular & Developmental Biology Animal, 46, 431-437.
63. Vogt, G., & Quinitio, E. T. (1994). Accumulation and excretion of metal granules in the prawn, Penaeus monodon, exposed to water-borne copper, lead, iron and calcium. Aquatic Toxicology, 28, 223-241.
64. Nimeth, K. T., Mahlknecht, M., Mezzanato, A., Peter, R., Rieger, R., & Ladurner, P. (2004). Stem cell dynamics during growth, feeding, and starvation in the basal flatworm Macrostomum sp. (Platyhelminthes). Developmental Dynamics, 230, 91-99.
65. Narbonne, P., & Roy, R. (2005). Inhibition of germline proliferation during C. elegans dauer development requires PTEN, LKB1 and AMPK signalling. Development, 133, 611-619.
66. Davis, L. E., & Burnett, A. L. (1964). A study of growth and cell differentiation in the hepatopancreas of the crayfish. Developmental Biology, 10, 122-153.
67. Söderhäll, I., Kim, Y.-A., Jiravanichpaisal, P., Lee, S.-Y., & Söderhäll, K. (2005). An ancient role for a prokineticin domain in invertebrate hematopoiesis. Journal of Immunology, 174, 6153-6160.
68. Lin, X., Novotny, M., Söderhäll, K., & Söderhäll, I. (2010). Ancient cytokines, the role of astakines as hematopoietic growth factors. Journal of Biological Chemistry, 285, 28577-28586.
69. Gherardi, F., Souty-Grosset, C., Vogt, G., Diéguez-Uribeondo, J., & Crandall, K. A. (2010). Infraorder Astacidea Latreille, 1802 p. p.: The freshwater crayfish. In F. R. Schram & J. C. von Vaupel Klein (Eds.), Treatise on zoology - anatomy, taxonomy, biology. The Crustacea, Vol. 9, Part A: Eucarida: Euphausiacea, Amphionidacea, and Decapoda (partim) (pp. 269-423). Leiden: Brill.
70. Harrison, P. J. H., Cate, H. S., Swanson, E. S., & Derby, C. D. (2001). Postembryonic proliferation in the spiny lobster antennular epithelium: rate of genesis of olfactory receptor neurons is dependent on molt stage. Journal of Neurobiology, 47, 51-66.
71. Johnson, P. T. (1980). Histology of the blue crab, Callinectes sapidus. New York: Praeger.
72. Vafopoulou, X., Laufer, H., & Steel, C. G. H. (2007). Spatial and temporal distribution of the ecdysteroid receptor (EcR) in haemocytes and epidermal cells during wound healing in the crayfish, Procambarus clarkii. General and Comparative Endocrinology, 152, 359-370.
73. Hopkins, P. M., Chung, A. C.-K., & Durica, D. S. (1999). Limb regeneration in the fiddler crab, Uca pugilator: histological, physiological and molecular considerations. American Zoologist, 39, 513-526.
74. Durica, D. S., Kupfer, D., Najar, F., Lai, H., Tang, Y., Griffin, K., et al. (2006). EST library sequencing of genes expressed during early limb regeneration in the fiddler crab and transcriptional responses to ecdysteroid exposure in limb bud explants. Integrative and Comparative Biology, 46, 948-964.
75. Franco, A., Jouaux, A., Mathieu, M., Sourdaine, P., Lelong, C., Kellner, K., et al. (2010). Proliferating cell nuclear antigen in gonad and associated storage tissue of the Pacific oyster Crassostrea gigas: seasonal immunodetection and expression in laser microdissected tissues. Cell and Tissue Research, 340, 201-210.
76. Obata, M., Sano, N., Kimata, S., Nagasawa, K., Yoshizaki, G., & Komaru, A. (2010). The proliferation and migration of immature germ cells in the mussel, Mytilus galloprovincialis: observation of the expression pattern in the M. galloprovincialis vasa-like gene (Myvlg) by in situ hybridization. Development, Genes and Evolution, 220, 139-149.
77. Zaldibar, B., Cancio, I., & Marigómez, I. (2004). Circatidal variation in epithelial cell proliferation in the mussel digestive gland and stomach. Cell and Tissue Research, 318, 395-402.
78. Casali, A., & Batlle, E. (2009). Intestinal stem cells in mammals and Drosophila. Cell Stem Cell, 4, 124-127.
79. Hine, P. M. (1999). The inter-relationships of bivalve haemocytes. Fish & Shellfish Immunology, 9, 367-385.
80. Cima, F., Matozzo, V., Marin, M. G., & Ballarin, L. (2000). Haemocytes of the clam Tapes philippinarum (Adams & Reeve, 1850): morphofunctional characterisation. Fish & Shellfish Immunology, 10, 677-693.
81. Matozzo, V., Marin, M. G., Cima, F., & Ballarin, L. (2008). First evidence of cell division in circulating haemocytes from the Manila clam Tapes philippinarum. Cell Biology International, 32, 865-868.
82. Acosta-Salmón, H., & Southgate, P. C. (2006). Wound healing after excision of mantle tissue from the Akoya pearl oyster, Pinctada fucata. Comparative Biochemistry and Physiology A, 143, 264-268.
83. Tomiyama, T., & Ito, K. (2006). Regeneration of lost siphon tissues in the tellinacean bivalve Nuttallia olivacea. Journal of Experimental Marine Biology and Ecology, 335, 104-113.
84. García-Arrarás, J. E., & Greenberg, M. J. (2001). Visceral regeneration in holothurians. Microscopy Research and Technique, 55, 438-451.
85. Mashanov, V. S., Zueva, O. R., Rojas-Catagena, C., & Garcia-Arraras, J. E. (2010). Visceral regeneration in a sea cucumber involves extensive expression of survivin and mortalin homologs in the mesothelium. BMC Developmental Biology, 10, 117.
86. Thorndyke, M. C., Chen, W.-C., Beesley, P. W., & Patruno, M. (2001). Molecular approach to echinoderm regeneration. Microscopy Research and Technique, 55, 474-485.
87. Candia Carnevali, M. D. (2006). Regeneration in echinoderms: repair, regrowth, cloning. Invertebrate Survival Journal, 3, 64-76.
88. García-Arrarás, J. E., & Dolmatov, I. Y. (2010). Echinoderms: potential model systems for studies on muscle regeneration. Current Pharmaceutical Design, 16, 942-955.
89. Ward, R. D., & Nishioka, D. (1993). Seasonal changes in testicular structure and localization of a sperm surface glycoprotein during spermatogenesis in sea urchins. Journal of Histochemistry and Cytochemistry, 41, 423-431.
90. Yakovlev, K. V., Battulin, N. R., Serov, O. L., & Odintsova, N. A. (2010). Isolation of oogonia from ovaries of the sea urchin Strongylocentrotus nudus. Cell and Tissue Research, 342, 479-490.
91. Holm, K., Dupont, S., Sköld, H., Stenius, A., Thorndyke, M., & Hernroth, B. (2008). Induced cell proliferation in putative haematopoietic tissues of the sea star, Asterias rubens (L.). Journal of Experimental Biology, 211, 2551-2558.
92. Pinsino, A., Thorndyke, M. C., & Matranga, V. (2007). Coelomocytes and post-traumatic response in the common sea star Asterias rubens. Cell Stress & Chaperones, 12, 331-341.
93. Ortiz-Pineda, P. A., Ramírez-Gómez, F., Pérez-Ortiz, J., González-Díaz, S., Santiago-De Jesús, F., Hernández-Pasos, J., et al. (2009). Gene expression profiling of intestinal regeneration in the sea cucumber. BMC Genomics, 10, 262.
94. Biressi, A. C. M., Zou, T., Dupont, S., Dahlberg, C., Di Benedetto, C., Bonasoro, F., et al. (2010). Wound healing and arm regeneration in Ophioderma longicaudum and Amphiura filiformis (Ophiuroidea, Echinodermata): comparative morphogenesis and histogenesis. Zoomorphology, 129, 1-19.
95. Hernroth, B., Farahani, F., Brunborg, G., Dupont, S., Dejmek, A., & Nilsson Sköld, H. (2010). Possibility of mixed progenitor cells in sea star arm regeneration. Journal of Experimental Zoology B, 314, 457-468.
96. Turksen, K. (Ed.). (2004). Adult stem cells. Totawa: Humana.
97. Odintsova, N. A. (2009). Stem cells of marine invertebrates: regulation of proliferation and induction of differentiation in vitro. Cell and Tissue Biology, 3, 403-408.
98. Rinkevich, B. (2011). Cell cultures from marine invertebrates: new insights for capturing endless stemness. Marine Biotechnology, 13, 345-354.
99. Weissman, I. L. (2000). Stem cells: units of development, units of regeneration, and units in evolution. Cell, 100, 157-168.
100. Murugesan, P., Balasubramanian, T., & Pandian, T. J. (2010). Does haemocoelom exclude embryonic stem cells and asexual reproduction in invertebrates? Current Science, 98, 768-771.
101. Bely, A. E. (2010). Evolutionary loss of animal regeneration: pattern and process. Integrative and Comparative Biology, 50, 515-527.
102. Katsube, K.-I., & Sakamoto, K. (2005). Notch in vertebrates - molecular aspects of the signal. International Journal of Developmental Biology, 49, 369-374.
103. Brand, A. H., & Livesey, F. J. (2011). Neural stem cell biology in vertebrates and invertebrates: more alike than different? Neuron, 70, 719-729.
104. Oviedo, N. J., Pearson, B. J., Levin, M., & Sánchez Alvarado, A. (2008). Planarian PTEN homologs regulate stem cells and regeneration through TOR signaling. Disease Models & Mechanisms, 1, 131-143.
105. Gustafson, E. A., & Wessel, G. M. (2010). Vasa genes: emerging roles in the germ line and in multipotent cells. Bioessays, 32, 626-637.
106. Sánchez Alvarado, A., & Tsonis, P. A. (2006). Bridging the regeneration gap: genetic insights from diverse animal models. Nature Reviews Genetics, 7, 873-884.
107. Yoshida-Noro, C., & Tochinai, S. (2010). Stem cell system in asexual and sexual reproduction of Enchytraeus japonensis (Oligochaeta, Annelida). Development, Growth & Differentiation, 52, 43-55.
108. Jopling, C., Boue, S., & Belmonte, J. C. I. (2011). Dedifferentiation, transdifferentiation and reprogramming: three routes to regeneration. Nature Reviews Molecular Cell Biology, 12, 79-89.
109. Nye, H. L. D., Cameron, J. A., Chernoff, E. A. G., & Stocum, D. L. (2003). Regeneration of the urodele limb: a review. Developmental Dynamics, 226, 280-294.
110. Masahito, P., Ishikawa, T., & Sugano, H. (1988). Fish tumors and their importance in cancer research. Japanese Journal of Cancer Research, 79, 545-555.
111. Newman, S. J., & Smith, S. A. (2006). Marine mammal neoplasia: a review. Veterinary Pathology, 43, 865-880.
112. Pompei, F., Polkanov, M., & Wilson, R. (2001). Age distribution of cancer in mice: the incidence turnover at old age. Toxicology and Industrial Health, 17, 7-16.
113. Spitsbergen, J. M., & Kent, M. L. (2003). The state of the art of the zebrafish model for toxicology and toxicologic pathology research - advantages and current limitations. Toxicologic Pathology, 31(Suppl), 62-87.
114. Feitsma, H., & Cuppen, E. (2008). Zebrafish as a cancer model. Molecular Cancer Research, 6, 685-694.
115. Anchelin, M., Murcia, L., Alcaraz-Pérez, F., García-Navarro, E. M., & Cayuela, M. L. (2011). Behaviour of telomere and telomerase during aging and regeneration in zebrafish. PLoS ONE, 6, e16955.
116. Lang, G. H., Wang, Y., Nomura, N., & Matsumura, M. (2004). Detection of telomerase activity in tissues and primary cultured lymphoid cells of Penaeus japonicus. Marine Biotechnology, 6, 347-354.
117. Klapper, W., Kühne, K., Singh, K. K., Heidorn, K., Parwaresh, R., & Krupp, G. (1998). Longevity of lobsters is linked to ubiquitous telomerase expression. FEBS Letters, 439, 143-146.