Blood, Vol. 89 No. 7 (April 1), 1997:
pp. 2611-2612
CORRESPONDENCE
Can Ferritin Provide Iron for Hemoglobin Synthesis?
 |
LETTER |
To the Editor:
We have read with great interest a recent report by Gelvan et al1 attempting to resurrect an old idea that immature erythroid cells obtain iron (Fe) from ferritin. We wish to comment on one single and extremely important issue in this report, viz, that Fe from internalized ferritin can be used for hemoglobin synthesis. We believe that neither the results of previous studies nor experiments presented by Gelvan et al1 provide adequate evidence supporting this claim.
In 1957 Bessis and Breton-Gorius2 presented electron micrographs depicting erythroblastic islands in the bone marrow, in which a central reticulum cell ("nurse cell") was surrounded by a ring of erythroblasts. In the region of contact between these cells the authors observed ferritin and proposed that it was transferred from the reticulum cell to the erythroblasts by a form of micropinocytosis termed "rhopheocytosis" (for review see ref 3). Somewhat later, Jandl, Katz, and coworkers4,5 showed that immature erythroid cells take up Fe from plasma Fe-binding protein, transferrin (Tf ), and suggested the existence of a membrane-bound Tf receptor which may be involved in Fe uptake. The many studies and discussions that followed have led to a general consensus that Tf, not ferritin, is the source of Fe for hemoglobin synthesis, and this view has been supported by the following evidence. First, under normal conditions all plasma Fe is associated with Tf, and ferrokinetic studies have provided clear evidence that all Fe used for hemoglobin synthesis passes through the plasma.6 Hence, if the reticulum cell ferritin was the source of hemoglobin Fe, these cells would have to acquire it from Tf. However, virtually no Fe enters the reticuloendothelial system from plasma Tf.7 Second, it should also be pointed out that plasma ferritin has a very low Fe content, and no ferrokinetic evidence supports its role in Fe transport.7 Third, a specific relationship between Tf and erythroid cells is documented by in vitro studies showing that this molecule is the only physiologically relevant Fe complex capable of providing Fe for hemoglobin synthesis.8 Fourth, normally developing erythroid cells take up 26 mg Fe/d from plasma Tf,7 a rate that matches almost perfectly with the daily production of hemoglobin (~6.2 g). The final and most convincing evidence of an absolute requirement for Tf by erythroid cells comes from observations that both humans and mice with hereditary atransferrinemia have severe hypochromic microcytic anemias.9-11 Furthermore, when compared with wild-type animals, hypotransferrinemic mice show an extremely restricted uptake of 59Fe by the erythron.12,13 Collectively, the above studies document the stringent dependency of erythroid cells on Tf-bound Fe. Interestingly, in 1962 Bessis and Breton-Gorius themselves reviewed critically their original hypothesis, and did not exclude the possibility that the phenomenon of "rhopheocytosis" takes place in the opposite direction, ie, "the erythroblast imparts the ferritin to the reticular cell."14
Ferritin is not only an improbable source of Fe for the erythroid cells, but it is also an unlikely mediator involved in intracellular translocation of Fe for heme synthesis. Although ferritin has been postulated to act as an intermediate for heme synthesis in erythroid cells,15,16 several studies failed to show that 59Fe from 59Fe-ferritin could be incorporated into hemoglobin.17,18 When heme synthesis was inhibited in erythroid cells incubated with 59Fe-transferrin, very little19,20 or no21 59Fe accumulates in ferritin. More importantly, when heme synthesis is restored in these cells, no 59Fe in ferritin was used for heme synthesis.20 These findings concur with observations that the intracellular Fe release from ferritin may require its catabolism,22 and suggests limited availability of ferritin Fe for metabolic purposes.
The evidence from previous studies showing that Tf and not ferritin is the Fe donor for hemoglobin synthesis must now be considered with the recent investigation by Gelvan et al.1 In this latter study the authors have incubated erythroid precursors with 59Fe-labeled ferritin for 21 hours, at which time they detected some 59Fe in the cells and in heme. Unfortunately, a number of technical flaws prevent the conclusion that 59Fe found in heme comes from 59Fe in the ferritin core. To prepare 59Fe-labeled ferritin, Gelvan and associates have exposed apoferritin to a mixture of 5% 59Fe(III) (as 59FeCl3 ) and 95% 56Fe(II) in an oxygenated buffer at pH 7.0. It is essential to point out that apoferritin shells can be loaded with Fe(II), whereas attempts to load Fe(III) into the core have failed.23 In their study, Gelvan et al probably presumed that 59Fe(III), in the presence of a large excess of unlabeled Fe(II), would be converted to 59Fe(II). However, in the absence of Fe-binding ligands such a conversion has been shown to occur only at an extremely low pH (<1.0, ref 24). From method description1 it is not apparent what ligand was present in the MOPS buffer that would stabilize both Fe(II) and Fe(III) in aqueous solution at pH 7.0 to allow electron self-exchange between the two redox states of Fe to occur. MOPS buffers are sometimes supplemented with EDTA (although this is not specified in ref 1) which, however, has almost 11 orders of magnitude higher formation constant for Fe(III) than for Fe(II).25 Hence, under aerobic conditions the Fe(II)-EDTA complex should be rapidly oxidized to Fe(III)-EDTA complex, but no reduction of 59Fe(III)-EDTA would occur. On the other hand, in the absence of any ligand, at pH 7.0, 59Fe(III) would be rapidly hydrolyzed into virtually insoluble ferric hydroxide polymers that could become nonspecifically associated with the external surface of ferritin shells.
The most troubling aspect of this study is that no attempt was made to determine that the 59Fe was actually present within the core of the ferritin molecule in contrast to nonspecifically bound to the surface. Hence, the physiological relevance of this ferritin preparation must be questioned. This poorly defined 59Fe-ferritin was then used for experiments at an Fe concentration of 6.5 mmol/L, ie, about 1,000-fold higher than the concentration of Fe found in the plasma under physiologic conditions. In addition, because the erythroblasts used in this study were not depleted of internalized Tf, it is possible that endocytosed Tf present within the cells could remove 59Fe from the surface of ferritin and donate it to the cells. It is also conceivable that some of the 59Fe(OH)3-polymers could be internalized by cells via nonspecific pinocytosis. Moreover, because of the aforementioned problems it is impossible to determine the specific radioactivity of 59Fe available for cellular uptake. Hence, it is impossible to estimate net Fe uptakes in terms of picomoles/106 cells, and no reasonable comparisons with Fe uptakes from Tf can be made. Apart from these problems, a number of important control experiments need to be completed before the physiological relevance of Fe uptake from ferritin can be postulated. These include time kinetics of 59Fe-ferritin uptake and saturability of 59Fe-ferritin uptake as a function of ferritin concentration. These latter studies need to be done with ferritin containing 59Fe in its core.
In conclusion, the experiments by Gelvan et al1 have not been adequately performed to conclude that ferritin plays a role as an Fe donor for hemoglobin synthesis. We strongly believe the investigators should repeat their experiments with ferritin, which has been definitely shown to contain 59Fe in its core. In combination with the additional controls described above, this strategy will then be appropriate to determine the role of ferritin in heme synthesis by erythroid cells.
Prem Ponka
Lady Davis Institute Jewish General Hospital Departments of Physiology and Medicine McGill University Montreal, Quebec, Canada
Des R. Richardson
Department of Physiology and Pharmacology School of Molecular Sciences James Cook University of North Queensland Townsville, Queensland, Australia
| |
ACKNOWLEDGMENT |
The authors thank Drs Ann English, Dennis Chasteen, Richard Frankel, and Gary Watt for many valuable discussions.
| |
REFERENCES |
1.
Gelvan D,
Fibach E,
Meyron-Holtz EG,
Konijn AM:
Ferritin uptake by human erythroid precursors is a regulated iron uptake pathway.
Blood
88:3200,
1996[Abstract/Free Full Text]
2.
Bessis MC,
Breton-Gorius J:
Iron particles in normal erythroblasts and normal and pathological erythrocytes.
J Biophys Biochem Cytol
3:503,
1957[Abstract/Free Full Text]
3. Bessis MC: Cytological aspects of hemoglobin production. The Harvey Lectures, Ser. 58, 1962-63, p 125
4.
Jandl JH,
Inman JK,
Simmons RL,
Allen DW:
Transfer of iron from serum iron-binding protein to human reticulocytes.
J Clin Invest
38:161,
1959
5.
Jandl JH,
Katz JH:
The plasma-to-cell cycle of transferrin in iron utilization.
J Clin Invest
42:314,
1963
6.
Pollycove M,
Mortimer R:
The quantitative determination of iron kinetics and hemoglobin synthesis in human subjects.
J Clin Invest
40:753,
1961
7. Bothwell TJ, Charlton RW, Cook JD, Finch CA: Iron Metabolism in Man. Oxford, UK, Blackwell Scientific, 1979
8.
Hemmaplardh D,
Morgan EH:
The mechanism of iron exchange between synthetic iron chelators and rabbit reticulocytes.
Biochim Biophys Acta
373:84,
1974[Medline]
[Order article via Infotrieve]
9.
Heilmeyer L:
Die atransferrinämien.
Acta Haematol
36:40,
1996
10.
Hamill RL,
Woods JC,
Cook BA:
Congenital atransferrinemia. A case report and review of the literature.
Am J Clin Pathol
96:215,
1991[Medline]
[Order article via Infotrieve]
11.
Bernstein SE:
Hereditary hypotransferrinemia with hemosiderosis, a murine disorder resembling human atransferrinemia.
J Lab Clin Med
110:690,
1987[Medline]
[Order article via Infotrieve]
12.
Craven CM,
Alexander T,
Eldridge M,
Kushner JP,
Bernstein S,
Kaplan J:
Tissue distribution and clearance kinetics of nontransferrin-bound iron in the hypotransferrinemic mouse: A rodent model for hemochromatosis.
Proc Natl Acad Sci USA
84:3457,
1987[Abstract/Free Full Text]
13.
Dickinson TK,
Devenyi AG,
Connor JR:
Distribution of injected iron 59 and manganese 54 in hypotransferrinemic mice.
J Lab Clin Med
128:270,
1996[Medline]
[Order article via Infotrieve]
14.
Bessis MC,
Breton-Gorius J:
Iron metabolism in the bone marrow as seen by electron microscopy. A critical review.
Blood
19:635,
1962[Abstract/Free Full Text]
15.
Mazur A,
Carleton A:
Relation of ferritin iron to heme synthesis in marrow and reticulocytes.
J Biol Chem
238:1817,
1963[Free Full Text]
16.
Nunez MT,
Glass J,
Robinson SH:
Mobilization of iron from the plasma membrane of the murine reticulocyte. The role of ferritin.
Biochim Biophys Acta
509:170,
1978[Medline]
[Order article via Infotrieve]
17.
Zail SS,
Charlton RW,
Torrance JD,
Bothwell TH:
Studies on the formation of ferritin in red cell precursors.
J Clin Invest
43:670,
1964
18.
Primosigh JV,
Thomas ED:
Studies on the partition of iron in bone marrow cells.
J Clin Invest
47:1473,
1968
19.
Ponka P,
Wilczynska A,
Schulman HM:
Iron utilization in rabbit reticulocytes. A study using succinylacetone as an inhibitor of heme synthesis.
Biochim Biophys Acta
720:96,
1982[Medline]
[Order article via Infotrieve]
20.
Richardson DR,
Ponka P,
Vyoral D:
Distribution of iron in reticulocytes after inhibition of heme synthesis with succinylacetone: Examination of intermediates involved in iron metabolism.
Blood
87:3477,
1996[Abstract/Free Full Text]
21.
Adams ML,
Ostapiuk I,
Grasso A:
The effects of inhibition of heme synthesis on the intracellular localization of iron in rat reticulocytes.
Biochim Biophys Acta
1012:243,
1989[Medline]
[Order article via Infotrieve]
22.
Pippard MJ,
Tikerpae J,
Peters TJ:
Ferritin iron metabolism in the rat liver.
Br J Haematol
64:839,
1986
23.
Harrison PM,
Arosio P:
The ferritins: Molecular properties, iron storage function and cellular regulation.
Biochim Biophys Acta
1275:161,
1996[Medline]
[Order article via Infotrieve]
24.
Silverman J,
Dodson RW:
The exchange reaction between the two oxidation states of iron in acid solution.
J Phys Chem
56:846,
1952
25. Harris DC: Quantitative Chemical Analysis (ed 3). New York, Freeman, 1991, p 285
Response
We fully agree with Drs Ponka and Richardson that transferrin is most likely the major iron donor for hemoglobin production in erythroid cells, as was also understandable from our report. However, because there is another major iron-protein in biologic systems, namely ferritin, our study dealt with the possibility that this iron-protein, or certain types of it, may be actively involved in iron transfer and utilization and does not serve exclusively for a dead-end storage purpose. Our results, working with early erythroid precursors,1,2 suggest such a role. This suggestion is backed by numerous other studies. Thus, Blight and Morgan3 showed that guinea pig reticulocytes take up ferritin by a receptor-mediated process and use its iron for heme synthesis. Moreover, the ferritin iron competed with iron derived from transferrin. Similarly, Nunez et al4 demonstrated ferritin-iron uptake and utilization for heme synthesis in rabbit reticulocytes. Ulvik and Romslo5 showed that ferritin iron can be used in the ferrochelatase reaction of isolated rat mitochondria. We have recently shown that iron of ferritin produced by human macrophages was incorporated into hemoglobin when these macrophages were co-incubated with early erythroid cells.6 Based on our and others studies, we suggest that the transferrin pathway is by no means the only one. The "consensus" that transferrin is the only source for heme iron in erythroid cells is unfounded. The fact that atransferrinemic mice and humans still synthesize hemoglobin, albeit at lower levels than healthy individuals, enabling them to survive, supports this view, since in the absence of transferrin ferritin is the only potential iron donor.
Regarding the technical questions raised by Ponka and Richardson, we regret that our attempt to be concise resulted in a misconception. Indeed, the labeling of apoferritin with 59Fe was done in MOPS buffer pH 7.0 with no additional Fe binding ligands. However, equilibration between Fe(II) and Fe(III) was achieved in 0.1N HCl. The iron loading was performed essentially as described by Levi et al,7 MOPS buffer was chosen over MES buffer because the autoxidation rate of iron in MOPS was slower than in any of several other Good buffers tested, thereby decreasing the tendency for the formation of nonferritin ferric-hydroxypolymers. Small amounts of such polymer and aggregated ferritin, as evident from Treffry et all,8 were essentially removed by filtration before the use of the ferritin preparation, as shown by polyacrylamide gel electrophoresis under nonreducing conditions followed by autoradiography. The incorporation of the ferritin associated iron into the iron core under the conditions used has been strongly established.7,8 Our previous study established that free or protein-associated iron-hydroxypolymers, not incorporated in the ferritin core, dissolve during staining with Prussian blue. However, our ferritin-associated iron was unaffected by this stain, strongly indicating iron incorporating into the ferritin core rather than its accumulation on the protein surface. Thus, we believe that all necessary precautions have been taken to ensure the propriety and purity of the ferritin administered to the cells.
In conclusion, we do not dispute the role of transferrin as the main iron donor to erythroid cells; however, we do not accept the notion that it is the only molecule capable of performing this function.
Abraham M. Konijn
Dan Gelvan
Esther Meyron-Holtz
Department of Human Nutrition and Metabolism The Hebrew University Faculty of Medicine
Eitan Fibach
Department of Hematology The Hebrew University Faculty of Medicine Jerusalem, Israel
| |
REFERENCES |
1.
Fibach E,
Manor D,
Oppenheim A,
Rachmilewitz EA:
Proliferation and maturation of human erythroid progenitors in liquid culture.
Blood
73:100,
1989[Abstract/Free Full Text]
2.
Gelvan D,
Fibach E,
Meyron-Holtz EG,
Konijn AM:
Ferritin uptake by human erythroid precursors is a regulated iron uptake pathway.
Blood
88:3200,
1996
3.
Blight GD,
Morgan EH:
Ferritin and iron uptake by reticulocytes.
Br J Haematol
55:59,
1983[Medline]
[Order article via Infotrieve]
4.
Nunez MT,
Cole ES,
Glass J:
Cytosol intermediates in the transport of iron.
Blood
55:1051,
1980[Abstract/Free Full Text]
5.
Ulvik R,
Romslo I:
Studies on the utilization of ferritin iron in the ferrochelatase reaction of isolated rat liver mitochondria.
Biochim Biophys Acta
541:251,
1978[Medline]
[Order article via Infotrieve]
6. Konijn AM, Vaisman B, Meyron-Holtz EG, Leimberg JM, Rouault TA, Fibach E: Human erythroid precursors utilize and sense intra- and extra cellular ferritin iron. Blood 88:489a, 1996 (abstr, suppl 1)
7. Levi S, Luzzago A, Cesareni G, Cozzi A, Fraceschinelli F, Albertini A, Arosio P: Mechanism of ferritin iron uptake: Activity of the H-chain and deletion mapping of the ferro-oxidase site. A study of iron uptake and ferro-oxidase activity of human liver, recombinant H-chain ferritins, and of two H-chain deletion mutants.
8.
Treffry A,
Gelvan D,
Konijn AM,
Harrison PM:
Ferritin does not accumulate iron oxidized by caeruloplasmin.
Biochem J
305:21,
1995
