Literature DB >> 810611

Variations in the frequency of fetal hemoglobin-bearing erythrocytes (F-cells) in well adults, pregnant women, and adult leukemics.

S H Boyer, T K Belding, L Margolte, A N Noyes, P J Burke, W R Bell.   

Abstract

Fetal hemoglobin (HbF) in adult life is usually restricted to a few erythrocytes called F-cells. Their presence can be detected and the quantity of HbF per F-cell estimated by pericellular immunodiffusion reactions with anti-HbF. In normal adults F-cell frequency (range: 1 F-cell per 25 erythrocytes to 1 per 6800) and the mean amount of HbF per F-cell (range: approximately 14 to 28% of mean cell hemoglobin), although they are variables, remain constant over many months. Frequencies are similar in men and women. For a given individual, F-cell lifetimes are probably similar to those of other erythrocytes. F-cell production is not appreciably influenced by short term exposure to high altitude (approximately 4300 m) hypoxia. F-cell frequencies are briefly but substantially increased in many women during midpregnancy. In some women, presumptive 5- to 15-fold increases in F-cell production result in observed 3- to 7-fold increases in F-cell frequency during the 23rd to 31st weeks of gestation. These increases in F-cell frequency arise from selective alterations in maternal erythropoiesis and not from transplacental bleeding from the fetus. Substantial increases in F-cell frequency also occur in most adults with acute leukemia. In both pregnancy and leukemia, F-cell contributions of HbF are sufficient to account for modest elevations found in hemolysate HbF levels.

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Year:  1975        PMID: 810611

Source DB:  PubMed          Journal:  Johns Hopkins Med J        ISSN: 0021-7263


  7 in total

1.  Stimulation of fetal hemoglobin synthesis in bone marrow cultures from adult individuals.

Authors:  T H Papayannopoulou; M Brice; G Stamatoyannopoulos
Journal:  Proc Natl Acad Sci U S A       Date:  1976-06       Impact factor: 11.205

2.  Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.

Authors:  S H Boyer; L Margolet; M L Boyer; T H Huisman; W A Schroeder; W G Wood; D J Weatherall; J B Clegg; R Cartner
Journal:  Am J Hum Genet       Date:  1977-05       Impact factor: 11.025

3.  Hemoglobin F synthesis in vitro: evidence for control at the level of primitive erythroid stem cells.

Authors:  T Papayannopoulou; M Brice; G Stamatoyannopoulos
Journal:  Proc Natl Acad Sci U S A       Date:  1977-07       Impact factor: 11.205

4.  Detection and quantitation of the fetal hemoglobin variant Hb F-Malta-I in adults.

Authors:  G Altay; F Garver; W H Bannister; J L Grech; A Felice; T H Huisman
Journal:  Biochem Genet       Date:  1977-10       Impact factor: 1.890

5.  Proportion of fetal hemoglobin synthesis decreases during erythroid cell maturation.

Authors:  D H Chui; S C Wong; M W Enkin; M Patterson; R A Ives
Journal:  Proc Natl Acad Sci U S A       Date:  1980-05       Impact factor: 11.205

6.  Genetic regulation of gamma gene expression: study of the interaction of beta-thalassemia with heterocellular HPFH.

Authors:  A M Soummer; U Testa; P Dujardin; A Guerrasio; A Henri; M Gazaix; J Riou; H Rochant; Y Beuzard; J Rosa
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Genetic control of quantitative variation in carbonic anhydrase isozymes of mammals. I. The concentration within single erythrocytes of the mouse.

Authors:  S S Hsu; R E Tashian
Journal:  Biochem Genet       Date:  1977-10       Impact factor: 1.890

  7 in total

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