Duodenal expression of a putative stimulator of Fe transport and transferrin receptor in anemia and hemochromatosis

被引:13
作者
Barisani, D
Parafioriti, A
Armiraglio, E
Meneveri, R
Conte, D
机构
[1] IRCCS, Osped Maggiore, Dipartimento Sci Med, Cattedra Gastroenterol, I-20122 Milan, Italy
[2] Osped Gaetano Pini, Dept Pathol, Milan, Italy
[3] Univ Milano Bicocca, Dipartimento Med Sperimentale Ambientale & Biotec, Monza, Italy
关键词
D O I
10.1053/gast.2001.23946
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Stimulator of Fe Transport (SFT) and transferrin receptor (TfR) are proteins involved in iron transport. This study evaluated iron metabolism protein expression in duodenal biopsy specimens from controls and patients with abnormal iron metabolism. Methods: Twelve controls, 8 patients with iron deficiency anemia, 7 with HFE-related hemochromatosis, and 6 with non-HFE-related iron overload were studied. immunohistochemistry was performed on duodenal biopsy specimens with anti-TfR and anti-SFT antibodies which recognize a putative stimulator of Fe transport of similar to 80 kilodaltons, Results: In controls, the putative stimulator of Fe transport was expressed in the middle and distal part of the villi in the subapical cytoplasmatic region. Its expression increased in anemics and, to a lesser degree, in HFE-related hemochromatotics, whereas it was reduced in patients with non-HFE-related iron overload, TfR expression showed a crypt-to-tip gradient in controls, but not in anemics, in whom it was uniformly overexpressed. TfR expression was intermediate in HFE-related hemochromatotics and similar to controls in non-HFE-related iron overload. Conclusions: Expression of the putative stimulator of Fe transport and TfR increases in iron deficiency, Increased expression of both proteins is present only in HFE-related hemochromatotics suggesting that other factors may be involved in determining non-HFE-related iron overload phenotype.
引用
收藏
页码:1404 / 1411
页数:8
相关论文
共 50 条
  • [1] A novel mammalian iron-regulated protein involved in intracellular iron metabolism
    Abboud, S
    Haile, DJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (26) : 19906 - 19912
  • [2] Control of iron absorption
    Anderson, GJ
    [J]. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1996, 11 (11) : 1030 - 1032
  • [3] Intestinal iron absorption: current concepts circa 2000
    Andrews, NC
    [J]. DIGESTIVE AND LIVER DISEASE, 2000, 32 (01) : 56 - 61
  • [4] THE PATHOLOGY OF HEPATIC IRON OVERLOAD - A FREE-RADICAL MEDIATED PROCESS
    BACON, BR
    BRITTON, RS
    [J]. HEPATOLOGY, 1990, 11 (01) : 127 - 137
  • [5] Experimental hemochromatosis due to MHC class IHFE deficiency:: Immune status and iron metabolism
    Bahram, S
    Gilfillan, S
    Kühn, LC
    Moret, R
    Schulze, JB
    Lebeau, A
    Schümann, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (23) : 13312 - 13317
  • [6] TRANSFERRIN RECEPTORS IN THE HUMAN GASTROINTESTINAL-TRACT - RELATIONSHIP TO BODY IRON STORES
    BANERJEE, D
    FLANAGAN, PR
    CLUETT, J
    VALBERG, LS
    [J]. GASTROENTEROLOGY, 1986, 91 (04) : 861 - 869
  • [7] Crystal structure of the hereditary haemochromatosis protein HFE complexed with transferrin receptor
    Bennett, MJ
    Lebrón, JA
    Bjorkman, PJ
    [J]. NATURE, 2000, 403 (6765) : 46 - 53
  • [8] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [9] The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
    Camaschella, C
    Roetto, A
    Cali, A
    De Gobbi, M
    Garozzo, G
    Carella, M
    Majorano, N
    Totaro, A
    Gasparini, P
    [J]. NATURE GENETICS, 2000, 25 (01) : 14 - 15
  • [10] Overexpression of the hereditary hemochromatosis protein, HFE, in HeLa cells induces an iron-deficient phenotype
    Corsi, B
    Levi, S
    Cozzi, A
    Corti, A
    Altimare, D
    Albertini, A
    Arosio, P
    [J]. FEBS LETTERS, 1999, 460 (01) : 149 - 152