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Immature erythroid cells with novel morphology and cytoskeletal organization in adultXenopus

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Summary

Nucleated erythrocytes of non-mammalian vertebrates are a useful model system for studying the correlation between changes in cell shape and cytoskeletal organization during cellular morphogenesis. They are believed to transform from spheres to flattened discs to ellipsoids. Our previous work on developing erythroblasts suggested that pointed cells containing incomplete, pointed marginal bands (MBs) of microtubules might be intermediate stages in the larval axolotl. To test whether the occurrence of such pointed cells was characteristic of amphibian erythrogenesis, we have utilized phenylhydrazine (PHZ)-induced anemia in adultXenopus. In this system, circulating erythrocytes are destroyed and replaced by erythroblasts that differentiate in the blood, making them experimentally accessible. Thus, we followed the time-course of morphological and cytoskeletal changes in the new erythroid population during recovery. During days ∼ 7–9 post-PHZ, pointed cells did indeed begin to appear, as did spherical and discoidal cells. The percentage of pointed cells peaked at days ∼ 11–13 in different animals, subsequently declining as the percentage of elliptical cells increased. Since degenerating “old” erythrocytes were still present when pointed cells appeared, we tested directly whether pointed ones were “old” or “new” cells. Blood was removed via the dorsal tarsus vein, and the erythrocytes washed, fluorescently tagged, and re-injected. In different animals, ∼ 2–8% of circulating erythrocytes were labeled. Subsequent to induction of anemia in these frogs, time-course sampling showed that no pointed cells were labeled, identifying them as “new” cells. Use of propidium iodide revealed large nuclei and cytoplasmic staining indicative of immaturity, and video-enhanced phase contrast and anti-tubulin immunofluorescence showed that the pointed cells contained pointed MBs. The results show that pointed cells, containing incomplete, pointed MBs are a consistent feature of amphibian erythrogenesis. These cells may represent intermediate stages in the formation of elliptical erythrocytes.

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Abbreviations

MB:

marginal band

MS:

membrane skeleton

PHZ:

phenylhydrazine

References

  • Aleporou V, Maclean N (1978) Feedback inhibition of erythropoiesis induced in anaemicXenopus. J Embryol Exp Morphol 43: 221–231

    Google Scholar 

  • Altland, PD, Brace KC (1962) Red cell life span in the turtle and toad. Am J Physiol 203: 1188–1190

    Google Scholar 

  • Barrett LA, Dawson RB (1974) Avian erythrocyte development: microtubules and the formation of the disk shape. Dev Biol 36: 72–81

    Google Scholar 

  • —, Scheinberg SL (1972) The development of avian red cell shape. J Exp Zool 182: 1–14

    Google Scholar 

  • Behnke O (1993) The formation of fusiform proplatelets and their transformation to discoid platelets. Platelets 4: 262–267

    Google Scholar 

  • Chegini N, Aleporou V, Bell G, Hilder VA, Maclean N (1979) Production and fate of erythroid cells in anaemicXenopus laevis. J Cell Sci 35: 403–415

    Google Scholar 

  • Cohen WD (1982) The cytomorphic system of anucleate non-mammalian erythrocytes. Protoplasma 113: 23–32

    Google Scholar 

  • — (1986) Association of centrioles with the marginal band in skate erythrocytes. Biol Bull 171: 338–349

    Google Scholar 

  • — (1991) The cytoskeletal system of nucleated erythrocytes. Int Rev Cytol 130: 37–84

    Google Scholar 

  • —, Cohen MF, Tyndale-Biscoe CH, VandeBerg JL, Ralston GB (1990) The cytoskeletal system of mammalian primitive erythrocytes: studies in developing marsupials. Cell Motil Cytoskeleton 16: 133–145

    Google Scholar 

  • Dorn AR, Broyles RH (1982) Erythrocyte differentiation during the metamorphic hemoglobin switch ofRana catesbeiana. Proc Natl Acad Sci USA 79: 5592–5596

    Google Scholar 

  • DuPasquier L, Flajnik MF, Guiet C, Hsu E (1985) Methods used to study the immune system ofXenopus (Amphibia, Anura). In: Lefkovits I, Pernis B (eds) Immunological methods, vol III. Academic Press, New York, pp 425–465

    Google Scholar 

  • Ginsburg MF (1991) Cellular morphogenesis and the cytoskeleton in amphibian erythrocytes. PhD dissertation, City University of New York, New York, USA

    Google Scholar 

  • —, Twersky LH, Cohen WD (1989) Cellular morphogenesis and the formation of marginal bands in amphibian splenic erythroblasts. Cell Motil Cytoskeleton 12: 157–168

    Google Scholar 

  • Goniakowska-Witalinska L, Witalinski W (1977) Occurrence of micro tubules during erythropoiesis inLlama glama. J Zool 181: 309–313

    Google Scholar 

  • Hadji-Azimi I, Coosemans V, Canicatti C (1987) Atlas of adultXenopus laevis hematology. Dev Comp Immunol 11: 807–874

    Google Scholar 

  • Hollyfield JG (1966) Erythrocyte replacement at metamorphosis in the frogRana pipiens. J Morphol 119: 1–6

    Google Scholar 

  • Jones KH, Kniss DA (1987) Propidium iodide as a nuclear counterstain for immunofluorescence studies on cells in culture. J Histochem Cytochem 35: 123–125

    Google Scholar 

  • Jordan HE, Speidel CC (1930) Blood formation in cyclostomes. Am J Anat 46: 355–391

    Google Scholar 

  • Joseph-Silverstein J, Cohen WD (1984) The cytoskeletal system of nucleated erythrocytes. III. Marginal band function in mature cells. J Cell Biol 98: 2118–2125

    Google Scholar 

  • Lucas AM, Jamroz C (1961) Atlas of avian hematology. US Government Printing Office, Washington, DC (US Department of Agriculture monograph 25)

    Google Scholar 

  • Morin DE, Garry FB, Weiser MG, Fettman MJ, Johnson LW (1992) Hematologic features of iron deficiency anemia in llamas. Vet Pathol 29: 400–404

    Google Scholar 

  • Nemhauser I, Joseph-Silverstein J, Cohen WD (1983) Centrioles as microtubule-organizing centers for marginal bands of molluscan erythrocytes. J Cell Biol 96: 979–989

    Google Scholar 

  • Novikoff P, Cammer M, Satir P, Wolkoff AW (1992) Microtubule, actin filament, and ER distribution in untreated and taxol-treated cultured rat hepatocytes: analysis by confocal laser microscopy. Mol Biol Cell 3: 48 a

    Google Scholar 

  • Rugh R (1962) Experimental embryology. Burgess, Minneapolis

    Google Scholar 

  • Slezak SE, Horan PK (1989) Fluorescent in vivo tracking of hematopoietic cells. Part I. Technical considerations. Blood 74: 2171–2177

    Google Scholar 

  • Small JV, Davies HG (1972) Erythropoiesis in the yolk sac of the early chick embryo: an electron microscope and microspectro-photometric study. Tissue Cell 4: 341–378

    Google Scholar 

  • Smith BB, Reed PJ, Pearson EG, Long P, Lassen D, Watrous BJ, Lovelady S, Sims DE, Snyder SP (1991) Erythrocyte dyscrasia, anemia, and hypothyroidism in chronically underweight llamas. JAVMA 198: 81–88

    Google Scholar 

  • Sugiyama S (1926) Origin of thrombocytes and of the different types of blood cells as seen in the living chick blastoderm. Carnegie Inst Wash 18: 123–147

    Google Scholar 

  • Thomas N, Maclean N (1974) The blood as an erythropoietic organ in anaemicXenopus. Experientia 30: 1083–1085

    Google Scholar 

  • — — (1975) The erythroid cells of anemicXenopus laevis. I. Studies on cellular morphology and protein and nucleic acid synthesis during differentiation. J Cell Sci 19: 509–520

    Google Scholar 

  • Winckler B, Solomon F (1991) A role for microtubule bundles in the morphogenesis of chicken erythrocytes. Proc Natl Acad Sci USA 88: 6033–6037

    Google Scholar 

  • Wu M, Gerhart J (1991) RaisingXenopus in the laboratory. In: Kay BK, Peng HB (eds) Methods in cell biology, vol 36,Xenopus laevis: practical uses in cell and molecular biology. Academic Press, New York, pp3–18

    Google Scholar 

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Twersky, L.H., Bartley, A.D., Rayos, N. et al. Immature erythroid cells with novel morphology and cytoskeletal organization in adultXenopus . Protoplasma 185, 37–49 (1995). https://doi.org/10.1007/BF01272752

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