Haemoglobin switching in human embryos: asynchrony of ζ → α and ε → γ-globin switches in primitive and definitive erythropoietic lineage

作者: C. Peschle , F. Mavilio , A. Carè , G. Migliaccio , A. R. Migliaccio

DOI: 10.1038/313235A0

关键词:

摘要: Haemoglobin switching in humans provides a unique model for investigating the mechanisms underlying expression of developmentally regulated gene family. Numerous studies have focused on switch from fetal to adult (that is, gamma----beta) globin, but little is known about embryonic----fetal zeta----alpha and epsilon----gamma) switches, as well transition 'primitive' yolk sac 'definitive' liver erythropoiesis. Here we studied haemoglobin switches sac, circulating blood erythroblasts 25 embryos 6 fetuses. Globin synthesis was also evaluated purified erythroblasts. Primitive synthesize essentially zeta epsilon chains at 5 weeks alpha- epsilon-globin with minor aliquot gamma 6-7 weeks, whereas definitive produce alpha + beta-globin only beta 8 onward. In both lineages epsilon----gamma are asynchronous, former preceding latter. Furthermore, zeta- restricted primitive respectively. These findings discussed terms monoclonal early human ontogeny.

参考文章(17)
Endre Kelemen, Wenceslao Calvo, Theodor M. Fliedner, Atlas of Human Hemopoietic Development ,(2013)
Paul A. Marks, John S. Kovach, Chapter 8 Development of Mammalian Erythroid Cells Current Topics in Developmental Biology. ,vol. 1, pp. 213- 252 ,(1966) , 10.1016/S0070-2153(08)60014-9
F. Hecht, A. G. Motulsky, R. J. Lemire, T. E. Shepard, Predominance of hemoglobin Gower 1 in early human embryonic development. Science. ,vol. 152, pp. 91- 92 ,(1966) , 10.1126/SCIENCE.152.3718.91
Giuseppe Salvo, Patrizia Caprari, Paola Samoggia, Gualtiero Mariani, Anna Maria Salvati, Human erythrocyte separation according to age on a discontinuous "Percoll" density gradient. Clinica Chimica Acta. ,vol. 122, pp. 293- 300 ,(1982) , 10.1016/0009-8981(82)90290-X
Blanche P. Alter, Sabra C. Goff, Electrophoretic separation of human embryonic globin demonstrates “α-thalassemia” in human leukemia cell line K562 Biochemical and Biophysical Research Communications. ,vol. 94, pp. 843- 848 ,(1980) , 10.1016/0006-291X(80)91311-X
R. E. GALE, J. B. CLEGG, E. R. HUEHNS, Human embryonic haemoglobins Gower 1 and Gower 2 Nature. ,vol. 280, pp. 162- 164 ,(1979) , 10.1038/280162A0
GEORGE CASSADY, Monitoring, Birth Defects and Environment: The Problem of Surveillance. Archives of Pediatrics & Adolescent Medicine. ,vol. 124, pp. 458- 458 ,(1972) , 10.1001/ARCHPEDI.1972.02110150156042
W. G. WOOD, Haemoglobin synthesis during human fetal development. British Medical Bulletin. ,vol. 32, pp. 282- 287 ,(1976) , 10.1093/OXFORDJOURNALS.BMB.A071376
William Bloom, G. W. Bartelmez, Hematopoiesis in young human embryos American Journal of Anatomy. ,vol. 67, pp. 21- 53 ,(1940) , 10.1002/AJA.1000670103