The Importance of Roots in Regulating the Senescence of Soybean Primary Leaves

The role of roots in regulating primary leaf senescence of 14-day-old soybean seedlings was investigated. Compared with intact seedlings, the senescence of primary leaves is accelerated by removal of the root system but delayed if apical bud and the first trifoliate leaf are removed. No difference in senescence was found between intact seedlings and seedlings without roots, apical bud, and first trifoliate leaf. Lateral roots seem to play a predominant role in regulating primary leaf senescence. However, neither root nodules nor primary root play any function in senescence. Results indicate that benzyladenine (BA) at optimal concentration (2 mg/1) completely replaces the roots to prevent the senescence of primary leaves, whereas gibberellic acid (GA) and abscisic acid (ABA) accelerate. The effect of indole-3-acetic acid (IAA) to replace roots in preventing senescence depends on the season the young seedlings are grown. Additional, though indirect, information of acropetal transport of ABA is provided. In conclusion, it seems that cytokinins in lateral roots play a predominant role in leaf senescence and the normal supply of root cytokinins is important in leaf metabolism.     

Translocation of Sulfate in Soybean (Glycine max L. Merr)

Sulfate translocation in soybean (Glycine max L. Merr) was investigated. More than 90% of the sulfate entering the shoot system was recoverable in one or two developing trifoliate leaves. In young plants, the first trifoliate leaf contained between 10 to 20 times as much sulfate as the primary leaves, even though both types of leaf had similar rates of transpiration and photosynthesis. We conclude that most of the sulfate entering mature leaves is rapidly loaded into the phloem and translocated to sinks elsewhere in the plant. This loading was inhibited by carbonylcyanide m-chlorophenylhydrazone and selenate. At sulfate concentrations below 0.1 millimolar, more than 95% of the sulfate entering primary leaves was exported. At higher concentrations the rate of export increased but so did the amount of sulfate remaining in the leaves. Removal of the first trifoliate leaf increased two-fold the transport of sulfate to the apex, indicating that these are competing sinks for sulfate translocated from the primary leaves. The small amount of sulfate transported into the mesophyll cells of primary leaves is a result of feedback regulation by the intracellular sulfate pool, not a consequence of their metabolic inactivity. For example, treatment of plants with 2 millimolar aminotriazole caused a 700 nanomoles per gram fresh weight increase in the glutathione content of primary leaves, but had no effect on sulfate aquisition.     

Influence of magnesium deficiency on rates of leaf expansion, starch and sucrose accumulation, and net assimilation in Phaseolus vulgaris

Twenty one-day-old Phaseolus vulgaris 'Saxa'plants were cultured in a growth chamber and the plants supplied with either a complete or a Mg-free nutrient solution. From 6 days after transfer to the Mg-free solution, the rate of increase of the area of the second trifoliate leaf was considerably reduced; by day 11 the sucrose concentration in the first trifoliate leaf had increased 6. 2-fold at the end of the dark period and 4. 6-fold after the light period as compared with the control plants. Corresponding starch concentrations increased 6. 6-fold and 2. 9-fold respectively. After days 5 to 6 the assimilation rates declined in the first trifoliate leaf of the plants showing deficiency, in comparison with the plants fully supplied with nutrients; respiration increased during darkness. The reduction in net assimilation rate was to a great extent reversible after resupply of magnesium.
The reduction of magnesium concentration in the deficient plants was much more marked in the expanding leaves than in the mature primary leaves and roots. Sucrose and starch accumulation did not occur when the first trifoliate leaf was partially shaded, although magnesium concentration, as in the unshaded leaves, was reduced to 13% of that of the control plants. The consequences of magnesium deficiency in the expanding first trifoliate leaf are discussed in terms of the possibility of sink limitation.     

Effect of Removing Cotyledons, Apical Growing Region, or Trifoliate Leaves on the Growth and Growth-substance Content of Dwarf French Bean (Phaseolus vulgaris)

The growth of the primary leaf on intact plants was comparedwith that on plants from which the cotyledons, apical growingregion, or trifoliate leaves had been removed. Removing thecotyledons early decreased the final area of the primary leaves,this response being partially accounted for by a decrease intheir cell number, and increased the concentration (but notthe quantity) of gibberellin and auxin in them. This responsewas not altered by applying any of several growth substances.Early removal of the apical growing region increased the finalarea of the primary leaves; it also increased the gibberellincontent and concentration at Day 10 but did not influence theauxin content and concentration. Primary leaf expansion wasaffected less by detaching young trifoliate leaves than by removingthe entire apical growing region.     

Influence of spectral quality on the growth response of intact bean plants to brassinosteroid, a growth-promoting steroidal lactone. II. Chlorophyll content and partitioning of assimilate

The chlorophyll content and partitioning of assimilate of bean ( Phaseolus vulgaris L. 'Pinto') plants were determined 6 days after treatment of the second internode (I₂ with 5 μg of brassinosteroid (BR), a growth-promoting steroidal lactone. Plants were grown for 6 days under equal levels (90 μmol s^-1 m^-2) of photosynthetic photon flux density (PPFD) provided by cool white fluorescent (CWF) or incandescent (INC) lamps and equal levels of far-red (28 W m^-2, 700–800 nm) radiation provided by the same INC or far-red (FR) fluorescent lamps. Brassinosteroid treatment had no appreciable effect on total biomass production but caused a decrease of 15–20% dry matter distribution in the upper portion of the shoot, a small (4%) but constant increase in dry matter in l₂ and a large (11–16%) increase in dry matter in the lower portion of the shoot (especially I₁). Treatment with BR increased assimilate accumulation in the primary leaves, especially under INC and FR lamps, and reduced dry matter in the trifoliate leaves. BR also caused a 16–21% reduction in total leaf area and even a greater reduction in area of the trifoliate leaves, but significantly increased specific leaf weight of the primary leaves and the first trifoliate leaf and the amount of dry matter in the lateral shoots under all radiation sources. In comparison to controls, BR treatment increased dry matter accumulation in the treated internode 3.3x under CWF and 1.6x under INC or FR. BR treatment also increased chlorophyll content in the primary leaves under all radiation sources and in the trifoliate leaves under CWF and INC lamps. These findings suggest a possible mobilization role of BR and establish the importance of adequate PPFD (and photosynthate) for maximum swelling and splitting response to brassinosteroid.     

Alterations in source-sink patterns by modifications of source strength

Bean plants, trimmed to a simplified “double source, double sink” translocation system (the paired primary leaves serving as the double source and the paired lateral leaflets of the immature first trifoliate leaf as the double sink) were used to study the magnitude and short-term time course of change in the allocation ratio (partition ratio) of assimilates translocated from the labeled primary leaf to its respective “near” and “far leaflet” sinks in response to an increase or decrease in the source strength of the opposite primary leaf (the “control” leaf). If the rates of net photosynthesis in the two primary leaves were similar, assimilates from the labeled source leaf partitioned to the leaflet sinks in the ratio of 5:1 or higher, the dominant sink being the leaflet “nearer” to the labeled source leaf. If the rate of net photosynthesis in the control leaf was increased substantially above that of the labeled source leaf, the rate of translocation from the labeled source to either the near leaflet sink or far leaflet sink remained unaffected, despite, presumably, a higher translocation rate from the control leaf, and hence a higher phloem pressure gradient (or increased cross-sectional area) in the transport pathway from the control leaf to the leaflet sinks. If the control leaf was excised, thus reducing the source leaf area by about a half, the translocation rate from the remaining source leaf rapidly doubled, the partition ratio becoming equal to unity. If the control leaf was darkened, the partition ratio adjusted to an intermediate value. Although export rates from the labeled source leaf were increased either by excising or darkening the control leaf, the rate of net photosynthesis in the labeled leaf remained constant.     

THE EFFECT OF GIBBERELLIC ACID ON THE ABSORPTION AND TRANSLOCATION OF PHOSPHORUS-32 BY BEAN PLANTS

Linck , A. J., and Theodore W. Sudia . (U. Minnesota, St. Paul.) The effect of gibberellic acid on the absorption and translocation of phosphorus-32 by bean plants. Amer. Jour. Bot. 47(2) : 101—105. Illus. 1960.–Plants of Phaseolus vulgaris, variety ‘Black Valentine,‘ treated with 1 p.p.m. gibberellic acid supplied to the roots for 4 hr. were compared with nontreated. plants for phosphorus-32 uptake. Plants treated with gibberellic acid where transpiration was either rapid or restricted absorbed more phosphorus-32 than those not treated. More phosphorus-32 was recovered from plants free to transpire than from plants in high humidity. In plants free to transpire, significantly more phosphorus was present in the treated plants after 28 hr. and significantly more phosphorus-32 accumulated in treated plants in those parts actively growing, i.e., stem apex, second internode and first trifoliate leaf, and in the roots. For plants in high humidity atmosphere significantly more phosphorus-32 was absorbed by the treated plants at the end of 4 hr. than in the non-treated plants and this difference was maintained throughout all times of harvest. For plants in high humidity atmosphere, significantly more phosphorus-32 accumulated in the lower portions, i.e., roots, hypocotyl, first internode and primary leaves, of treated plants than of non-treated plants, while the differences for the second internode, the first trifoliate leaf and the stem apex were not significant between treated and non-treated plants.     

不同pH值下丛枝菌根真菌对枳生长及铁吸收的影响

摘要：【目的】本文对营养液不同pH值下丛枝菌根(arbuscular mycorrhiza)真菌地表球囊霉（Glomus versiforme）对枳[Poncirus trifoliata]实生苗生长及植株铁营养状况的影响进行了初步研究。【方法】采用盆栽砂培试验,分别施浇pH 5.0、6.0、7.0和8.0的霍格兰营养液（含50 μM Fe-EDTA）;常规方法测定植株生长指标;曲利苯蓝染色法测定菌根侵染率;分光光度法测定叶绿素含量和根系三价铁螯合物还原酶活性;原子吸收分光光度法测定叶片钾和活性铁含量;钒     

Transport of 14C-Assimilates in Seedlings of Phaseolus vulgaris L. in Relation to Vascular Anatomy

Patterns of ¹⁴C-photosynthate translocation in bean (Phaseolusvulgaris L.) seedlings have been investigated in relation tovascular-bundle continuity between exporting and importing organsby use of radioassay and tissue-clearing techniques. Assimilatefrom the primary leaves reaches the first trifoliate leaf byan indirect route. There is no direct vascular connection betweenthe primary leaves and distal tissues. Bundles of the primaryleaf petiole connect with an anastomosis at the node, and allbundles which originate from this structure descend the stem.Assimilate from primary leaves moves down the stem, and is thentransferred to an ascending pathway, the bundles of which traversethe anastomosis at the second node. The lateral leaflets ofthe first trifoliate leaf are served differentially by primaryleaves with respect to assimilate supply. Differences are relatedto position, and may be accounted for by differences in vascularcontinuity.     

Photosynthetic Response to Water Stress in Phaseolus vulgaris

Water stressed Phaseolus vulgaris L. plants were monitored to detect the relationships between net photosynthesis, transpiration, boundary layer plus stomatal resistance, mesophyll resistance, CO₂ compensation point, ribulose, 1,5-diphosphate carboxylase activity and leaf water potential. At full expansion, the first trifoliate leaves of greenhouse grown bean plants were subjected to water stress by withholding irrigation. Gas exchange and enzyme activity of the central trifoliolate leaflets were monitored as leaf water potential decreased. Although increased stomatal resistance appeared to be the primary causal factor of reduced net photosynthesis, increased mesophyll resistance and decreased ribulose 1,5-diphosphate carboxylase activity further documented the role of non-stomatal factors.     

Regulation of Photosynthetic Activity in the Primary Leaves of Bean (Phaseolus vulgaris L.) by Materials Moving in the Water-conducting System

Endogenous factors which determine the photosynthetic capacity of the leaf were studied in the fully expanded, primary leaves of young seedings of bean (cv. Bulgarian). Following removal of the shoot above the primary leaf node and excision of all axillary buds, the primary leaves increased in area and thickness, in chlorophyll content, in levels of soluble protein, and in the specific activity of ribulose-1,5-bisphosphate carboxylase. Plants in which phloem continuity was disrupted by heat-girdling of the stem, between the shoot above the primary leaf node and the organs below, did not exhibit similar increases, whereas the shoot above the girdle continued to grow for several days. Plants in which all developing trifoliate leaves were excised as soon as they became macroscopic exhibited an increase in their photosynthetic activity, area, and thickness, while their main stem and (leafless) branches made considerable growth. Transpiration from the primary leaves was the same in decapitated plants as in the heat-girdled ones, although in the latter it accounted for only about 30% of total transpiration.     

Metabolism and distribution of cyclohexanecarboxylic Acid, a plant growth stimulant, in bush bean

A foliar spray of 10 mm cyclohexanecarboxylic acid (CHC), a component of the growth stimulant naphthenic acid, to primary leaves of 14-day-old plants of bush bean, Phaseolus vulgaris L., cv Top Crop, resulted in increased vegetative growth and pod production. One minute after the application of 0.5 mm CHC-7-(14)C (CHC(*)) to a primary leaf, CHC(*) was present within it. The chief conversion of the CHC(*) in the leaf during the interval 15 minutes to 4 hours after the acid had been applied appeared to be CHC(*) to its glucose conjugate (CHC(*)-G), and during 4 to 48 hours, CHC(*)-G to CHC(*)-aspartate and an unknown metabolite. Radioactivity was confined to the leaf for at least 1 hour, but by the 12th hour was detected throughout the plant. In the interval 1 to 4 weeks after CHC(*) application, the mean percentage distribution of radioactivity was: treated leaf, 65.3; roots, 18.8; stem, 7.7; trifoliate leaves, 5.9; flower buds-flowers-pods, 2.3. During this period CHC(*)-G was the most prominent metabolite in all organs; no free CHC(*) was detected. Light favored the movement of CHC(*) conjugates out of the leaf; glucose fed to dark-grown plants substituted for light to some extent but aspartate was relatively ineffective, suggesting the dependence of outward movement on ATP. The presence of the glucose and aspartate conjugates of the acid in all organs of CHC-treated plants and the absence of free CHC from them suggest that one or both conjugates, rather than the acid itself, are involved in growth stimulation.     

外源EBR对NaCl胁迫下燕麦幼苗无机离子吸收、运输和分配的影响

为了探讨外源2,4-表油菜素内酯(2,4-epibrassinolide,EBR)诱导燕麦(Avena sativa L.)幼苗抗盐性的效果及其生理调节机制,以"青引2号"和"加燕2号"燕麦为材料,研究NaCl胁迫下施用外源EBR对燕麦幼苗无机离子吸收、运输和分配的影响。结果表明:100mmol·L-1NaCl胁迫下,"青引2号"和"加燕2号"燕麦幼苗叶片和根系中的Na+、Cl-含量均显著升高,对阳离子的吸收产生了拮抗作用,导致燕麦幼苗叶片和根系中的K+、Ca2+、Mg2+、Mn2+、Fe2+、Zn2+、Cu2+含量显著降低,离子稳态平衡被打破; 100 mmol·L-1NaCl胁迫下,施用0.01μmol·L-1外源EBR后,"青引2号"和"加燕2号"燕麦幼苗叶片和根系中的Na+和Cl-含量显著降低,促进了燕麦幼苗根系对K+、Ca2+、Mg2+、Fe2+、Mn2+、Cu2+和Zn2+的吸收,叶片和根系中K+/Na+、Cl-/Na+、Ca2+/Na+、Mg2+/Na+、Fe2+/Na+、Mn2+/Na+、Cu2+/Na+和Zn2+/Na+显著升高,并且有效调控燕麦幼苗体内无机离子的运输...     

Benzyladenine-Directed Transport of Carbon-14 and Phosphorus-32 in Senescing Bean Plants

The distribution of radioactivity from applied sucrose.¹⁴C and³²P to various plant parts were studied in relation to the retardationof leaf senescence by applied benzyladenine (BA) in intact beanplants. In short-time experiments sucrose-¹⁴C was fed to theplants for 48 h through the second trifoliate leaf at weeklyintervals from the third to the eighth week after planting.In long-term experiments sucrose-¹⁴C was fed to all plants for48 h at the third week and changes in distribution examinedat weekly intervals up till the eight week. In both cases, BAapplied to the primary leaves of intact bean plants did notcause a directed mobilization of sucrose-¹⁴C. When the plantswere stripped, leaving the primary leaves and the terminal pod,and fed sucrose-¹⁴C or ³²P through the terminal leaflet of thesecond trifoliate leaf, the BA-treated leaf accumulated relativelymore radioactivity than the opposite water-treated leaf. Itwas concluded that the retardation of senescence by BA in theprimary leaves of intact bean plants does not result directlyfrom the mobilization of metabolites and nutrients from otherplant parts. It is therefore suggested that BA-induced longevityin the primary leaves of the intact plant is accomplished bymetabolic self-sustenance.     

Studies on Foliar Penetration: IX. PATTERNS OF PENETRATION OF 2,4-DICHLOROPHENOXYACETIC ACID INTO THE LEAVES OF DIFFERENT SPECIES

The comparative patterns of penetration of 2,4-dichlorophenoxyaceticacid (2,4-D) into the leaves of Phaseolus vulgaris, Zea mays,Pisum sativum, Beta wlgaris, Helianthus annuus and Gossypiumhirsuium have been examined. Save for Zea and Gossypium where there is little change withthe stage of leaf development the rates of penetration intoboth surfaces decrease as the leaf matures. The relative ratesare dependent on the species and the age of the leaf but thereare differences between the surfaces. In Phaseolus the characteristicsof primary leaves differ from those of trifoliate leaves sinceonly in immature trifoliate leaves is penetration into the adaxialsurface greater. In darkness the rates of penetration over 24 h remain constantor fall but slightly for all species. Light consistently promotespenetration but with Beta there is a lag before entry is acceleratedinto the abaxial surface as has previously been reported foryoung primary leaves of Phaseolus. For the remaining speciesthe courses of penetration in both light and darkness into bothsurfaces follow similar patterns. As the light intensity isincreased entry is enhanced but the limit of response variesbetween species, between surfaces within species, and in trifoliateleaves of Phaseolus with age. For the six species the order of the relative rates of entryis closely similar whether comparisons are made in light ordarkness or between abaxial and adaxial surfaces: viz. Zea >Helianthus > Phaseolus (primary) > Phaseolus (trifoliate)> Pisum = Beta = Gossypium. The observed specific differencesare discussed in relation to variations in leaf structure, theproperties and thickness of the cuticle and the physiologicaland metabolic processes which influence transport within theepidermal tissues after it has passed through the cuticle bydiffusion.     

Auxin is required for leaf vein pattern in Arabidopsis

To investigate possible roles of polar auxin transport in vein patterning, cotyledon and leaf vein patterns were compared for plants grown in medium containing polar auxin transport inhibitors (N-1-naphthylphthalamic acid, 9-hydroxyfluorene-9-carboxylic acid, and 2,3,5-triiodobenzoic acid) and in medium containing a less well-characterized inhibitor of auxin-mediated processes, 2-(p-chlorophynoxy)-2-methylpropionic acid. Cotyledon vein pattern was not affected by any inhibitor treatments, although vein morphology was altered. In contrast, leaf vein pattern was affected by inhibitor treatments. Growth in polar auxin transport inhibitors resulted in leaves that lacked vascular continuity through the petiole and had broad, loosely organized midveins, an increased number of secondary veins, and a dense band of misshapen tracheary elements adjacent to the leaf margin. Analysis of leaf vein pattern developmental time courses suggested that the primary vein did not develop in polar auxin transport inhibitor-grown plants, and that the broad midvein observed in these seedlings resulted from the coalescence of proximal regions of secondary veins. Possible models for leaf vein patterning that could account for these observations are discussed.     

Auxin Functions Downstream of Ethylene to Regulate Iron Absorption Promoted by Phomopsis liquidambaris in Arachis hypogaea L.

Plant iron (Fe) deficiency is widely present in alkaline calcium soils worldwide, and endophytes show great potential for promoting plant nutrient absorption. However, the underlying mechanisms remain unclear. To clarify the mechanisms by which the endophytic fungus Phomopsis liquidambaris promotes peanut Fe absorption, we designed this study to detect the physiological changes in peanut with P. liquidambaris infection. We measured ethylene and auxin in peanuts under Fe deficiency and found that fungal colonization promoted their accumulation (50% and 20%, respectively, at the top point). Moreover, plant Fe absorption ability and transfer were enhanced according to qPCR and enzyme results; the Fe content in the leaf increased (29.52%) as the symptoms of leaf chlorosis were ameliorated. Finally, the chlorophyll content increased (29%), and plant growth was enhanced (13.3%). We also proved that during Fe insufficiency, auxin functions downstream of ethylene to induce the upregulation of Fe absorption-related gene and enzyme activity including that of AHA4, IRT1, H⁺-ATPase, and FCR. We conclude that the addition of P. liquidambaris activates the auxin signaling pathway downstream of ethylene and improves peanut Fe absorption by promoting rhizosphere acidification, increasing FCR and IRT1 expression in peanut roots, leading to plant Fe absorption and growth.

     

Metabolic responses in iron deficient tomato plants

The effects of Fe deficiency on different metabolic processes were characterized in roots, xylem sap and leaves of tomato. The total organic acid pool increased significantly with Fe deficiency in xylem sap and leaves of tomato plants, whereas it did not change in roots. However, the composition of the pool changed with Fe deficiency, with major increases in citrate concentrations in roots (20-fold), leaves (2-fold) and xylem sap (17-fold). The activity of phosphoenolpyruvate carboxylase, an enzyme leading to anaplerotic C fixation, increased 10-fold in root tip extracts with Fe deficiency, whereas no change was observed in leaf extracts. The activities of the organic acid synthesis-related enzymes malate dehydrogenase, citrate synthase, isocitrate dehydrogenase, fumarase and aconitase, as well as those of the enzymes lactate dehydrogenase and pyruvate carboxylase, increased with Fe deficiency in root extracts, whereas only citrate synthase increased significantly with Fe deficiency in leaf extracts. These results suggest that the enhanced C fixation capacity in Fe-deficient tomato roots may result in producing citrate that could be used for Fe xylem transport. Total pyridine nucleotide pools did not change significantly with Fe deficiency in roots or leaves, although NAD(P)H/NAD(P) ratios were lower in Fe-deficient roots than in controls. Rates of O(2) consumption were similar in Fe-deficient and Fe-sufficient roots, but the capacity of the alternative oxidase pathway was decreased by Fe deficiency. Also, increases in Fe reductase activity with Fe deficiency were only 2-fold higher when measured in tomato root tips. These values are significantly lower than those found in other plant species, where Fe deficiency leads to larger increases in organic acid synthesis-related enzyme activities and flavin accumulation. These data support the hypothesis that the extent of activation of different metabolic pathways, including carbon fixation via PEPC, organic acid synthesis-related enzymes and oxygen consumption is different among species, and this could modulate the different levels of efficiency in Strategy I plants.     

铁胁迫对三种柑橘砧木的生长、生理特性及铁分布的影响

以枳壳、酸橙和红橘三种柑橘砧木实生苗为材料,采用溶液培养法研究了铁胁迫对其生长、生理特性及铁分布的影响.结果表明:缺铁胁迫(0 μmol·L-1)时,三种柑橘砧木的生长指标及叶片叶绿素含量均显著低于低铁(5 μmol·L-1)和适量铁(50 μmol·L-1)处理;三者叶片和根系的POD、CAT活性显著降低,SOD活性...     

Iron absorption and hepatic iron uptake are increased in a transferrin receptor 2 (Y245X) mutant mouse model of hemochromatosis type 3

Hereditary hemochromatosis type 3 is an iron (Fe)-overload disorder caused by mutations in transferrin receptor 2 (TfR2). TfR2 is expressed highly in the liver and regulates Fe metabolism. The aim of this study was to investigate duodenal Fe absorption and hepatic Fe uptake in a TfR2 (Y245X) mutant mouse model of hereditary hemochromatosis type 3. Duodenal Fe absorption and hepatic Fe uptake were measured in vivo by 59Fe-labeled ascorbate in TfR2 mutant mice, wild-type mice, and Fe-loaded wild-type mice (2% dietary carbonyl Fe). Gene expression was measured by real-time RT-PCR. Liver nonheme Fe concentration increased progressively with age in TfR2 mutant mice compared with wild-type mice. Fe absorption (both duodenal Fe uptake and transfer) was increased in TfR2 mutant mice compared with wild-type mice. Likewise, expression of genes participating in duodenal Fe uptake (Dcytb, DMT1) and transfer (ferroportin) were increased in TfR2 mutant mice. Nearly all of the absorbed Fe was taken up rapidly by the liver. Despite hepatic Fe loading, hepcidin expression was decreased in TfR2 mutant mice compared with wild-type mice. Even when compared with Fe-loaded wild-type mice, TfR2 mutant mice had increased Fe absorption, increased duodenal Fe transport gene expression, increased liver Fe uptake, and decreased liver hepcidin expression. In conclusion, despite systemic Fe loading, Fe absorption and liver Fe uptake were increased in TfR2 mutant mice in association with decreased expression of hepcidin. These findings support a model in which TfR2 is a sensor of Fe status and regulates duodenal Fe absorption and liver Fe uptake.