Literature DB >> 2351065

Temporal and spatial selection against parthenogenetic cells during development of fetal chimeras.

R H Fundele1, M L Norris, S C Barton, M Fehlau, S K Howlett, W E Mills, M A Surani.   

Abstract

The fate of parthenogenetic cells was investigated during development of fetal and early postnatal chimeras. On day 13 of embryonic development, considerable contribution of parthenogenetic cells was observed in all tissues of chimeric embryos, although selection against parthenogenetic cells seemed to start before day 13. Between days 13 and 15 of development, parthenogenetic cells came under severe selective pressure, which was most striking in tongue. The disappearance of parthenogenetic cells from tongue coincided with the beginning of myoblast fusion in this tissue. Severe selection against parthenogenetic cells was also observed in pancreas and liver, although in the latter, parthenogenetic cells were eliminated later than in skeletal muscle or pancreas. In other tissues, parthenogenetic cells may persist and participate to a considerable extent throughout the gestation period and beyond, although a significant decrease was observed in all tissues. Parthenogenetic in equilibrium fertilized chimeras were significantly smaller than their non-chimeric littermates at all developmental stages. These results suggest that the absence of paternal chromosomes is largely incompatible with the maintenance of specific differentiated cell types. Furthermore, paternally derived genes seem to be involved in the regulation of proliferation of all cell types, as indicated by the drastic growth decceleration of parthenogenetic in equilibrium fertilized chimeras and the overall decrease of parthenogenetic cells during fetal development. Chromosomal imprinting may have a role in maintaining a balance between cell growth and differentiation during embryonic development. The major exception to the selective elimination of parthenogenetic cells appear to be the germ cells; viable offspring derived from parthenogenetic oocytes were detected, sometimes at a high frequency in litters of female parthenogenetic in equilibrium fertilized chimeras.

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Year:  1990        PMID: 2351065     DOI: 10.1242/dev.108.1.203

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  21 in total

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Authors:  J W Gordon; M W Bradbury
Journal:  J In Vitro Fert Embryo Transf       Date:  1991-02

2.  Hematopoietic reconstitution with androgenetic and gynogenetic stem cells.

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Review 3.  Parthenotes as a source of embryonic stem cells.

Authors:  T A L Brevini; F Gandolfi
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4.  In vivo and in vitro differentiation of uniparental embryonic stem cells into hematopoietic and neural cell types.

Authors:  Sigrid Eckardt; Timo C Dinger; Satoshi Kurosaka; N Adrian Leu; Albrecht M Müller; K John McLaughlin
Journal:  Organogenesis       Date:  2008-01       Impact factor: 2.500

5.  Global analysis of parental imprinting in human parthenogenetic induced pluripotent stem cells.

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Journal:  Nat Struct Mol Biol       Date:  2011-05-15       Impact factor: 15.369

6.  Distribution of androgenetic cells in fetal mouse chimeras.

Authors:  R Fundele; R Krause; S C Barton; M A Surani; B Christ
Journal:  Rouxs Arch Dev Biol       Date:  1995-08

7.  Parthenogenetic stem cells for tissue-engineered heart repair.

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Journal:  J Clin Invest       Date:  2013-02-22       Impact factor: 14.808

Review 8.  Concise review: parthenote stem cells for regenerative medicine: genetic, epigenetic, and developmental features.

Authors:  Brittany Daughtry; Shoukhrat Mitalipov
Journal:  Stem Cells Transl Med       Date:  2014-01-17       Impact factor: 6.940

9.  Downregulation of H19 improves the differentiation potential of mouse parthenogenetic embryonic stem cells.

Authors:  Neli P Ragina; Karianne Schlosser; Jason G Knott; Patricia K Senagore; Pamela J Swiatek; Eun Ah Chang; Walid D Fakhouri; Brian C Schutte; Matti Kiupel; Jose B Cibelli
Journal:  Stem Cells Dev       Date:  2011-09-14       Impact factor: 3.272

10.  Brief report: Parthenogenetic embryonic stem cells are an effective cell source for therapeutic liver repopulation.

Authors:  Silvia Espejel; Sigrid Eckardt; Jack Harbell; Garrett R Roll; K John McLaughlin; Holger Willenbring
Journal:  Stem Cells       Date:  2014-07       Impact factor: 6.277

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