Literature DB >> 10475271

A protein from Naegleria amoebae causes apoptosis in chick embryo and CHO cells after they become confluent.

T H Dunnebacke1, K H Walen.   

Abstract

Exposure for less than an hour to a protein isolated from Naegleria amoebae initiates a process that has no apparent effect on the appearance or growth of chick embryo or CHO cell cultures for 4 to 9 days; after the development of confluency, at some unknown signal, all of the cells undergo an apoptotic death within a 12- to 24-hour period. Abnormalities detected among the last mitotic cells include chromosomal breakage and early reversal in metaphase to telo/interphase daughter nuclei with irregular shapes. Additional events in the dying cultures include the development of a cytoplasmic amoebic-related immunogen, gross DNA fragmentation, cell blebbing, shrinkage, and apoptotic body formation. Culture death included all cells, those present in confluent cultures when the protein was added, and in other cultures, those formed during a more than 30-fold increase in cells as the cultures became confluent. The increase in the number of cells followed by the uniformity and synchrony of their death pattern indicates that the signal to kill has increased and spread throughout the culture; upon an unknown condition related to confluency, events are initiated that lead to the unusual apoptotic death of the culture.

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Year:  1999        PMID: 10475271     DOI: 10.1007/s11626-999-0069-6

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol Anim        ISSN: 1071-2690            Impact factor:   2.416


  41 in total

1.  Internucleosomal DNA cleavage should not be the sole criterion for identifying apoptosis.

Authors:  R J Collins; B V Harmon; G C Gobé; J F Kerr
Journal:  Int J Radiat Biol       Date:  1992-04       Impact factor: 2.694

2.  Ongoing activity of RNA polymerase II precludes chromatin collapse and DNA fragmentation in Chinese hamster ovary cells.

Authors:  J Damgaard; Y Balslev; K Møllgaard; K Wassermann
Journal:  Biochem Biophys Res Commun       Date:  1996-10-23       Impact factor: 3.575

3.  Apoptosis of human lymphocytes in the absence or presence of internucleosomal DNA cleavage.

Authors:  M Marini; D Musiani; P Sestili; O Cantoni
Journal:  Biochem Biophys Res Commun       Date:  1996-12-24       Impact factor: 3.575

4.  The temporal relationship between protein phosphatase, ICE/CED-3 proteases, intracellular acidification, and DNA fragmentation in apoptosis.

Authors:  C M Wolf; J E Reynolds; S J Morana; A Eastman
Journal:  Exp Cell Res       Date:  1997-01-10       Impact factor: 3.905

5.  Classification of peptidases.

Authors:  A J Barrett
Journal:  Methods Enzymol       Date:  1994       Impact factor: 1.600

Review 6.  Cell death: the significance of apoptosis.

Authors:  A H Wyllie; J F Kerr; A R Currie
Journal:  Int Rev Cytol       Date:  1980

7.  Sequential acquisition of mitochondrial and plasma membrane alterations during early lymphocyte apoptosis.

Authors:  M Castedo; T Hirsch; S A Susin; N Zamzami; P Marchetti; A Macho; G Kroemer
Journal:  J Immunol       Date:  1996-07-15       Impact factor: 5.422

8.  Internucleosomal cleavage of DNA as the sole criterion for apoptosis may be artifactual.

Authors:  H Enright; R P Hebbel; K A Nath
Journal:  J Lab Clin Med       Date:  1994-07

Review 9.  Apoptosis. Its significance in cancer and cancer therapy.

Authors:  J F Kerr; C M Winterford; B V Harmon
Journal:  Cancer       Date:  1994-04-15       Impact factor: 6.860

10.  Cell nucleus and DNA fragmentation are not required for apoptosis.

Authors:  K Schulze-Osthoff; H Walczak; W Dröge; P H Krammer
Journal:  J Cell Biol       Date:  1994-10       Impact factor: 10.539

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