Adequacy of iron supply for erythropoiesis: in vivo observations in humans - PubMed (original) (raw)
Affiliations
- PMID: 3681115
Adequacy of iron supply for erythropoiesis: in vivo observations in humans
M Cazzola et al. J Lab Clin Med. 1987 Dec.
Abstract
The adequacy of tissue iron supply was examined with ferrokinetic techniques in subjects with decreased plasma iron concentration and in subjects with a normal plasma iron concentration but with increased tissue iron requirements. The competition by transferrin receptors for diferric vs monoferric transferrin was measured in eight normal persons and eight with iron deficiency. There was a highly significant (P less than 0.001) decrease in receptor preference for diferric transferrin in subjects with iron deficiency, indicating an insufficient amount of iron-bearing transferrin to saturate tissue receptors. The adequacy of the plasma iron supply was also examined by determining the number of iron-bearing transferrin molecules with receptors at normal and elevated plasma iron concentrations. Significant increases were found at the higher plasma iron concentration, not only in patients with iron deficiency, but also in patients with sickle cell anemia and thalassemia. Furthermore, the increase in the latter two groups was shown to be proportional to the degree of erythroid hyperplasia. These data indicate that tissue iron supply must be evaluated in terms of both plasma iron supply and erythropoietic requirements and that a relative iron deficiency is frequent in patients with erythroid hyperplasia.
Similar articles
- Ferrokinetic measurement of erythropoiesis.
Beguin Y, Stray SM, Cazzola M, Huebers HA, Finch CA. Beguin Y, et al. Acta Haematol. 1988;79(3):121-6. doi: 10.1159/000205743. Acta Haematol. 1988. PMID: 3128034 - [The transferrin receptor: its role in iron metabolism and its diagnosis utility].
Vernet M. Vernet M. Ann Biol Clin (Paris). 1999 Jan-Feb;57(1):9-18. Ann Biol Clin (Paris). 1999. PMID: 9920962 Review. French. - Erythropoietin and iron-restricted erythropoiesis.
Goodnough LT. Goodnough LT. Exp Hematol. 2007 Apr;35(4 Suppl 1):167-72. doi: 10.1016/j.exphem.2007.01.026. Exp Hematol. 2007. PMID: 17379103 Review.
Cited by
- Crosstalk between Iron Metabolism and Erythropoiesis.
Li H, Ginzburg YZ. Li H, et al. Adv Hematol. 2010;2010:605435. doi: 10.1155/2010/605435. Epub 2010 Jun 10. Adv Hematol. 2010. PMID: 20631898 Free PMC article. - Characterization of Putative Erythroid Regulators of Hepcidin in Mouse Models of Anemia.
Mirciov CS, Wilkins SJ, Dunn LA, Anderson GJ, Frazer DM. Mirciov CS, et al. PLoS One. 2017 Jan 30;12(1):e0171054. doi: 10.1371/journal.pone.0171054. eCollection 2017. PLoS One. 2017. PMID: 28135344 Free PMC article. - Iron deficiency anemia: a common and curable disease.
Miller JL. Miller JL. Cold Spring Harb Perspect Med. 2013 Jul 1;3(7):a011866. doi: 10.1101/cshperspect.a011866. Cold Spring Harb Perspect Med. 2013. PMID: 23613366 Free PMC article. Review. - Delayed hepcidin response explains the lag period in iron absorption following a stimulus to increase erythropoiesis.
Frazer DM, Inglis HR, Wilkins SJ, Millard KN, Steele TM, McLaren GD, McKie AT, Vulpe CD, Anderson GJ. Frazer DM, et al. Gut. 2004 Oct;53(10):1509-15. doi: 10.1136/gut.2003.037416. Gut. 2004. PMID: 15361505 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical