The liver plays a central role in iron metabolism. It is the major storage site for iron and also expresses a complex range of molecules which are involved in iron transport and regulation of iron homeostasis. An incr...The liver plays a central role in iron metabolism. It is the major storage site for iron and also expresses a complex range of molecules which are involved in iron transport and regulation of iron homeostasis. An increasing number of genes associated with hepatic iron transport or regulation have been identified. These include transferrin receptors （TFRI and 2）, a ferrireductase （STEAP3）, the transporters divalent metal transporter-1 （DMT1） and ferroportin （FPN） as well as the haemochromatosis protein, HFE and haemojuvelin （HJV）, which are signalling molecules. Many of these genes also participate in iron regulatory pathways which focus on the hepatic peptide hepcidin. However, we are still only beginning to understand the complex interactions between liver iron transport and iron homeostasis. This review outlines our current knowledge of molecules of iron metabolism and their roles in iron transport and regulation of iron homeostasis.展开更多
Non-HFE hereditary haemochromatosis （HH） refers to a genetically heterogeneous group of iron overload disorders that are unlinked to mutations in the HFE gene. The four main types of non-HFE HH are caused by mutatio...Non-HFE hereditary haemochromatosis （HH） refers to a genetically heterogeneous group of iron overload disorders that are unlinked to mutations in the HFE gene. The four main types of non-HFE HH are caused by mutations in the hemojuvelin, hepcidin, transferrin receptor 2 and ferroportin genes. Juvenile haemochromatosis is an autosomal recessive disorder and can be caused by mutations in either hemojuvelin or hepcidin. Ar~ adult onset form of HH similar to HFE-HH is caused by homozygosity for mutations in transferrin receptor 2. The autosomal dominant iron overload disorder ferroportin disease is caused by mutations in the iron exporter ferroportin. The clinical characteristics and molecular basis of the various types of non-HFE haemochromatosis are reviewed. The study of these disorders and the molecules involved has been invaluable in improving our understanding of the mechanisms involved in the regulation of iron metabolism.展开更多
Fe, Chlorophyll (Chl) and total nitrogen (TN) content in tissues were measured in Fe-deficient cultures of Ulva. pertusa over a period of 60 days. Photosynthetic carbon fixation rates were studied at the start of and ...Fe, Chlorophyll (Chl) and total nitrogen (TN) content in tissues were measured in Fe-deficient cultures of Ulva. pertusa over a period of 60 days. Photosynthetic carbon fixation rates were studied at the start of and 30 days after Fe-deficiency culture, when the effects of Fe-deficiency on the ultrastructure were also analyzed. The iron content in tissue decreased exponentially during Fe-deficiency (from 726.7 to 31.6 μg/gdw) and simultaneously Chl and TN content declined to 4.35% and 59.9% of their original levels respectively. Maximum carbon fixation rate (50-250 μmol/m 2 s) under Fe-deficiency decreased significantly compared with the control (p<0.01) and was 13.6 to 0.365 μg C /cm 2 h. Photosynthesis in Fe-deficient cells became light-saturated at lower irradiance than that in control. Ultrastructural observations of Fe-deficient cells showed reductions in chloroplast number, some degeneration of lamellar organization, an increase in vacuolar area, a decrease in mitochondrial matrix density, and variation in accumulation body number and morphology. During Fe-deficiency, the algae growth rate continued to decline and after 6 weeks of iron deficiency, no further growth was detectable. These suggested that the lower growth rate of Ulva. pertusa under Fe-deficiency could be due mainly to nitrogen utilization and inhibition of photosynthesis.展开更多
Cyanobacterial blooms are ubiquitous in fresh and brackish eutrophic waters in India. The cyanotoxins produced by many bloom forming cyanobacteria severely affect the health of animals, fishes, birds and human beings....Cyanobacterial blooms are ubiquitous in fresh and brackish eutrophic waters in India. The cyanotoxins produced by many bloom forming cyanobacteria severely affect the health of animals, fishes, birds and human beings. Different physical and chemical factors contribute towards bloom formation. Ten bloom forming cyanobacteria were isolated from natural blooms of northern India. The strains were purified and enriched in the laboratory. The aim of this study was to understand the influence of iron on growth, pigmentation and antioxidative activity of enzymes-catalase and ascorbate peroxidase of bloom forming cyanobacteria. Results show that different strains of bloom forming cyanobacteria attain optimum growth at varied concentration of iron. The cyanobacterial strains like Synechocystis aquatalis, Merismopedia glauca, Anabaena variabilis and Anabaena iyengarii exhibit maximum growth at low iron concentration （2 pM） while some species require higher concentration of iron for their optimum growth namely, Arthrospira platensis show optimum growth at 10uM, and Nostocpaludosum shows maximum growth at 100uM concentration of iron. It was also noticed that chlorophyll and phycobiliprotein content also varies with change in iron concentration. The activity of antioxidative enzymescatalase and ascorbate peroxidase was noticed in all ten cyanobacterial strains. In the light of the findings, it seems that Arthrospira platensis possess maximum catalase and ascorbate peroxidase activity. Increment in concentration beyond optimum value leads to deterioration in the growth, pigment content and enzymatic activity of the cyanobacterial strains. Knowledge about the factors influencing growth of bloom forming cyanobacteria will help to work out ways for eradication of hazardous cyanobacterial blooms.展开更多
基金The National Health and Medical Research Council of Australia
文摘The liver plays a central role in iron metabolism. It is the major storage site for iron and also expresses a complex range of molecules which are involved in iron transport and regulation of iron homeostasis. An increasing number of genes associated with hepatic iron transport or regulation have been identified. These include transferrin receptors （TFRI and 2）, a ferrireductase （STEAP3）, the transporters divalent metal transporter-1 （DMT1） and ferroportin （FPN） as well as the haemochromatosis protein, HFE and haemojuvelin （HJV）, which are signalling molecules. Many of these genes also participate in iron regulatory pathways which focus on the hepatic peptide hepcidin. However, we are still only beginning to understand the complex interactions between liver iron transport and iron homeostasis. This review outlines our current knowledge of molecules of iron metabolism and their roles in iron transport and regulation of iron homeostasis.
文摘Non-HFE hereditary haemochromatosis （HH） refers to a genetically heterogeneous group of iron overload disorders that are unlinked to mutations in the HFE gene. The four main types of non-HFE HH are caused by mutations in the hemojuvelin, hepcidin, transferrin receptor 2 and ferroportin genes. Juvenile haemochromatosis is an autosomal recessive disorder and can be caused by mutations in either hemojuvelin or hepcidin. Ar~ adult onset form of HH similar to HFE-HH is caused by homozygosity for mutations in transferrin receptor 2. The autosomal dominant iron overload disorder ferroportin disease is caused by mutations in the iron exporter ferroportin. The clinical characteristics and molecular basis of the various types of non-HFE haemochromatosis are reviewed. The study of these disorders and the molecules involved has been invaluable in improving our understanding of the mechanisms involved in the regulation of iron metabolism.
文摘Fe, Chlorophyll (Chl) and total nitrogen (TN) content in tissues were measured in Fe-deficient cultures of Ulva. pertusa over a period of 60 days. Photosynthetic carbon fixation rates were studied at the start of and 30 days after Fe-deficiency culture, when the effects of Fe-deficiency on the ultrastructure were also analyzed. The iron content in tissue decreased exponentially during Fe-deficiency (from 726.7 to 31.6 μg/gdw) and simultaneously Chl and TN content declined to 4.35% and 59.9% of their original levels respectively. Maximum carbon fixation rate (50-250 μmol/m 2 s) under Fe-deficiency decreased significantly compared with the control (p<0.01) and was 13.6 to 0.365 μg C /cm 2 h. Photosynthesis in Fe-deficient cells became light-saturated at lower irradiance than that in control. Ultrastructural observations of Fe-deficient cells showed reductions in chloroplast number, some degeneration of lamellar organization, an increase in vacuolar area, a decrease in mitochondrial matrix density, and variation in accumulation body number and morphology. During Fe-deficiency, the algae growth rate continued to decline and after 6 weeks of iron deficiency, no further growth was detectable. These suggested that the lower growth rate of Ulva. pertusa under Fe-deficiency could be due mainly to nitrogen utilization and inhibition of photosynthesis.
文摘Cyanobacterial blooms are ubiquitous in fresh and brackish eutrophic waters in India. The cyanotoxins produced by many bloom forming cyanobacteria severely affect the health of animals, fishes, birds and human beings. Different physical and chemical factors contribute towards bloom formation. Ten bloom forming cyanobacteria were isolated from natural blooms of northern India. The strains were purified and enriched in the laboratory. The aim of this study was to understand the influence of iron on growth, pigmentation and antioxidative activity of enzymes-catalase and ascorbate peroxidase of bloom forming cyanobacteria. Results show that different strains of bloom forming cyanobacteria attain optimum growth at varied concentration of iron. The cyanobacterial strains like Synechocystis aquatalis, Merismopedia glauca, Anabaena variabilis and Anabaena iyengarii exhibit maximum growth at low iron concentration （2 pM） while some species require higher concentration of iron for their optimum growth namely, Arthrospira platensis show optimum growth at 10uM, and Nostocpaludosum shows maximum growth at 100uM concentration of iron. It was also noticed that chlorophyll and phycobiliprotein content also varies with change in iron concentration. The activity of antioxidative enzymescatalase and ascorbate peroxidase was noticed in all ten cyanobacterial strains. In the light of the findings, it seems that Arthrospira platensis possess maximum catalase and ascorbate peroxidase activity. Increment in concentration beyond optimum value leads to deterioration in the growth, pigment content and enzymatic activity of the cyanobacterial strains. Knowledge about the factors influencing growth of bloom forming cyanobacteria will help to work out ways for eradication of hazardous cyanobacterial blooms.
