Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0005221,
umls-concept:C0007634,
umls-concept:C0015936,
umls-concept:C0017262,
umls-concept:C0033268,
umls-concept:C0062245,
umls-concept:C0205307,
umls-concept:C0369183,
umls-concept:C0439849,
umls-concept:C0521457,
umls-concept:C0681850,
umls-concept:C1261502,
umls-concept:C1550501,
umls-concept:C1706203,
umls-concept:C1882911,
umls-concept:C2349001,
umls-concept:C2697811
|
pubmed:issue |
4
|
pubmed:dateCreated |
1987-5-7
|
pubmed:abstractText |
We have developed methodology that allows comparison of the mean corpuscular hemoglobin (MCH) of fetal hemoglobin (HbF)-containing red cells (F cells) with the MCH of non-F cells from the same individual. To do this, suspensions of peripheral blood erythrocytes and their internal contents are fixed with an imidodiester, dimethyl-3,3'-dithiobispropionimidate dihydrochloride (DTBP). Thereafter fixed cells are made permeable to antisera by treatment with Triton X-100 and isopropanol, reacted with a mouse monoclonal antibody (MoAb) against HbF, and then with fluorescein-conjugated antimouse IgG. No appreciable hemoglobin is lost during such manipulation. Red cells from a diversity of subjects were thus treated and examined microscopically, first by transmitted light and then by epifluorescence. A direct correlation between Coulter-derived MCH and mean absorbance of 415 nm transmitted light was found for 100 unfixed (r = 0.96) and for 100 antibody-treated fixed-permeabilized red cells (r = 0.99) among individuals selected so as to provide a range of Coulter MCH values between 20 and 35. Comparisons of microscopically derived MCH of F cells and non-F cells were statistically nondistinguishable (P greater than 0.05) in all subjects. Such comparisons included normal individuals (less than 1% F cells), SS patients (7% to 48% F cells), subjects with congenital anemia (22% to 65% F cells), individuals with heterocellular hereditary persistence of HbF (HPFH) (12% to 21% F cells), and heterozygotes for beta + thalassemia (11% to 31% F cells). We conclude that gamma- and beta-globin production within F cells is regulated in a reciprocal fashion both among normal individuals and among individuals with elevated HbF production.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0006-4971
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
69
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1109-13
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:2435342-Anemia,
pubmed-meshheading:2435342-Anemia, Sickle Cell,
pubmed-meshheading:2435342-Antibodies, Monoclonal,
pubmed-meshheading:2435342-Erythrocytes,
pubmed-meshheading:2435342-Fanconi Anemia,
pubmed-meshheading:2435342-Fetal Hemoglobin,
pubmed-meshheading:2435342-Gene Expression Regulation,
pubmed-meshheading:2435342-Globins,
pubmed-meshheading:2435342-Hemoglobinopathies,
pubmed-meshheading:2435342-Humans,
pubmed-meshheading:2435342-Thalassemia
|
pubmed:year |
1987
|
pubmed:articleTitle |
Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin production.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|