Deficiency of α-1-antitrypsin influences systemic iron homeostasis.

There is evidence that proteases and antiproteases participate in the iron homeostasis of cells and living systems. We tested the postulate that α-1 antitrypsin (A1AT) polymorphism and the consequent deficiency of this antiprotease in humans are associated with a systemic disruption in iron homeostasis. Archived plasma samples from Alpha-1 Foundation (30 MM, 30 MZ, and 30 ZZ individuals) were analyzed for A1AT, ferritin, transferrin, and C-reactive protein (CRP). Plasma samples were also assayed for metals using inductively coupled plasma atomic emission spectroscopy (ICPAES). Plasma levels of A1AT in MZ and ZZ individuals were approximately 60% and 20% of those for MM individuals respectively. Plasma ferritin concentrations in those with the ZZ genotype were greater relative to those individuals with either MM or MZ genotype. Plasma transferrin for MM, MZ, and ZZ genotypes showed no significant differences. Linear regression analysis revealed a significant (negative) relationship between plasma concentrations of A1AT and ferritin while that between A1AT and transferrin levels was not significant. Plasma CRP concentrations were not significantly different between MM, MZ, and ZZ individuals. ICPAES measurement of metals confirmed elevated plasma concentrations of nonheme iron among ZZ individuals. Nonheme iron concentrations correlated (negatively) with levels of A1AT. A1AT deficiency is associated with evidence of a disruption in iron homeostasis with plasma ferritin and nonheme iron concentrations being elevated among those with the ZZ genotype.

Introduction

Alpha-1 antitrypsin (A1AT; also known as α-1 proteinase inhibitor) is a serum glycoprotein which predominantly (80%) originates from hepatocytes.1 A1AT inhibits a wide variety of proteases (eg, neutrophil elastase and proteinase-3) to contribute to a proteinase/antiproteinase balance.2 It is postulated that this acute phase protein participates in limiting host tissue injury by proteases at sites of inflammation;3 a proposed critical function is the prevention of lung injury associated with disruption of connective tissue by neutrophil elastase enzyme.1

A1AT deficiency is an autosomal recessive genetic disorder caused by its defective production leading to both decreased activity in body tissues and deposition of excessive abnormal protein in the liver.1,2 While M is the normal allele for A1AT, there are over 80 variant mutations of the gene. The Z allele results in a glutamate to lysine mutation at position 342 while the S allele produces a glutamate to valine mutation at position 264. In individuals with SS, MZ and SZ genotypes, blood levels of A1AT are reduced to between 40% and 60% of normal levels (ie, those observed among MM individuals). Among those who do not smoke, this A1AT concentration is almost always sufficient to protect the lungs from the effects of elastase. However, among individuals with the ZZ genotype, A1AT levels are usually less than 15% of normal and these deficient patients can develop lung disease at a young age. In addition, those with the ZZ genotype can develop liver disease; this is associated with impaired A1AT secretion and its consequent accumulation in this specific tissue. Therefore, A1AT deficient patients can present with lung disease (eg, panacinar emphysema [chronic obstructive pulmonary disease], pneumothorax, asthma, and bronchiectasis) and liver disease (eg, hepatitis, cirrhosis, and hepatocellular carcinoma).4 People of northern and western European ancestry are at the greatest risk for A1AT deficiency and its associated diseases;5 4% carry the PiZ allele and between 1 in 1,500 and 1 in 2,500–3,000 are ZZ.

In addition to siderophores and ferrireductases, microbials employ proteases to mobilize host sources of iron to support their growth and replication.6 These proteases cleave iron-transport and -storage proteins allowing utilization of the metal by the microbe.7,8 Corroborating a potential interaction between metal homeostasis and proteases, elevated iron concentrations impact expression of proteases and their activities.9–12 Animal and human investigation similarly suggests a participation of proteases in iron homeostasis.13–15 The intratracheal instillation of a single dose of neutrophil elastase in an animal model increased lung iron concentrations. Iron homeostasis is disrupted among cystic fibrosis patients in whom airway elastase content and activity is excessive; cystic fibrosis patients have elevated iron and ferritin concentrations in both the sputum and bronchoalveolar lavage.

A participation of proteases also suggests a potential involvement of anti-proteases in iron homeostasis. A1AT is the antiprotease in greatest concentration in humans. A participation of A1AT in the iron homeostasis of humans has been previously suggested with observations of deficient patients developing cirrhosis characterized by significant iron accumulation.16 An involvement of neutrophil elastase and A1AT in disrupting iron homeostasis of the lung was supported by investigation which demonstrated a proteolytic cleavage of both iron-transport and -storage proteins with subsequent increase in nonheme tissue iron concentrations.17 Finally, patients treated with antiproteases, and thus altering protease activity, can show evidence of disruptions in iron homeostasis.18 We further explored the relationship between A1AT and iron homeostasis in humans by testing the postulate that its deficiency is associated with a systemic disruption in iron homeostasis.

Methods

Samples from MM, MZ, and ZZ individuals

Archived plasma samples were kindly provided by the Alpha-1 Foundation (Miami, FL). These included 90 nonfasting plasma specimens from 30 MM, 30 MZ, and 30 ZZ individuals who had been screened as family members of a patient with A1AT deficiency. The health status of the donor was not known. Institutional Review Board exemption was granted from the University of North Carolina for analyses of these blood samples.

Plasma assays

Samples were analyzed for A1AT, ferritin, iron, transferrin, and C-reactive protein (CRP). A1AT and CRP concentrations were measured using immunoturbidimetric assay kits (DiaSorin Inc, Stillwater, MN). Ferritin was quantified by also using an immunoturbidimetric assay (Kamiya Biomedical Company, Seattle, WA). Transferrin concentrations were analyzed using an immunoprecipitin analysis (INCSTAR Corporation, Stillwater, MN). Assays were modified for use on the Konelab Arena 30 (ThermoLab Systems, Espoo, Finland).

Measurements of metals in plasma

Plasma samples were hydrolyzed at 70°C in 3 N HCl/10% trichloroacetic acid for 24 hours. After centrifugation, metals in the supernatant were measured using inductively coupled plasma optical emission spectroscopy (ICPOES; Model Optima 4300D; Perkin Elmer, Norwalk, CT).

Statistics

Data are expressed as mean values ± standard error unless otherwise specified. Differences between groups were compared using one-way analysis of variance. The post-hoc test employed was Duncan’s Multiple Range test. General linear regression modeling was used in delineating a relationship between two continuous variables. Significance was assumed at P < 0.05.

Results

Demographics of healthy individuals providing archived plasma samples are listed (Table 1). There were differences in the gender distributions between the MM, MZ, and ZZ cohorts and subsequently results were provided for males and females. Disparities in age and ethnicity between the cohorts were not significant.

Table 1

Demographics of healthy individuals providing plasma samples

	MM	MZ	ZZ
Males (n)	7	10	14
Females (n)	23	20	16
Age (years ± standard deviation)	52.2 ± 14.1	48.9 ± 15.9	50.3 ± 17.4
Caucasian (n)	25	27	25
African American (n)	3	0	0

Among the samples collected by the Alpha-1 Foundation, plasma levels of A1AT for MZ and ZZ individuals were approximated as 60% and 20% of those for MM individuals respectively (Figure 1A). This concentration of A1AT approximates those serum values reported in other study populations in which ZZ individual demonstrate levels 15% of MM subjects.19 There were significant differences in plasma ferritin concentrations between MM, MZ, and ZZ cohorts (Figure 1B). Those with the ZZ genotype showed greater ferritin values relative to both MM and MZ genotypes while there were no differences between MM and MZ (Figure 1B; F = 5.54; P = 0.02). When separate analyses of variance were conducted for males and females, the ferritin concentration in the ZZ cohort was greater than both MM and MZ for males while only greater than MM subjects for females. Plasma transferrin for MM, MZ, and ZZ cohorts showed no significant differences between them regardless of whether all were included in the analysis or sex-specific values were considered (Figure 1C; F = 2.97; P = 0.09).

Figure 1

Concentrations of A1AT, ferritin, and transferrin among MM, MZ, and ZZ cohorts. Relative to the MM genotype, significant decrements in plasma A1AT concentrations were observed in both MZ and ZZ subjects (A). Relative to MM subjects, plasma ferritin levels were significantly increased only in the ZZ cohort (B). Transferrin did not demonstrate differences between the three genotypes (C).

Notes: *Significant difference relative to the comparable sex-specific group of MM; **significant difference relative to the comparable sex-specific groups of MM and MZ.

Abbreviation: A1AT, α-1 antitrypsin.

Linear regression analysis revealed a significant (negative) relationship between plasma concentrations of A1AT and ferritin (Figure 2A; r = 0.26; P = 0.01). Linear regression between A1AT and transferrin levels was not significant (Figure 2B; r = 0.18; P = 0.09). The linear regression between ferritin and transferrin was significant (negative) (Figure 2C; r = 0.39; P < 0.01).

Figure 2

Linear correlations between plasma concentrations of A1AT, ferritin, and transferrin. The correlation between A1AT and ferritin concentrations (A) reached significance while that between A1AT and transferrin (B) did not. The relationship between plasma ferritin and transferrin was negative and significant (C).

Abbreviation: A1AT, α-1 antitrypsin.

Plasma CRP concentrations were not significantly different between MM, MZ, and ZZ individuals (Figure 3A). Linear regression analysis did not show a significant association between CRP and A1AT (Figure 3B; r = 0.10; P = 0.36). Regarding the relationships between CRP and indices of iron homeostasis, there was no significant association with either ferritin (r = 0.17; P = 0.11) or transferrin (r = 0.20; P = 0.06).

Figure 3

C-reactive protein (CRP) levels in MM, MZ, and ZZ individuals and its correlation with A1AT concentration. There were no significant differences in CRP among the MM, MZ, and ZZ genotypes (A). Similarly, there was no significant correlation between plasma A1AT and CRP concentrations (B).

Abbreviation: A1AT, α-1 antitrypsin.

Plasma metal concentrations were significantly different between MM and ZZ cohorts for aluminum (F = 3.10; P = 0.05) and iron (F = 3.37; P = 0.04) (Figure 4A). Zinc also appeared to increase in the ZZ cohort, but this did not reach significance (F = 0.49; P = 0.61). Aluminum and iron were elevated in those individuals with the ZZ genotype relative to the MM genotype; disparities between MM and MZ were not significant. In contrast, copper levels among those with both MZ and ZZ genotypes were significantly lower relative to the MM cohort (F = 4.33; P = 0.02) (Figure 4A). Correlations of plasma metal concentration with levels of A1AT were significant only for iron (Figure 3B; r = 0.21; P = 0.05).

Figure 4

Plasma metal concentrations among MM, MZ, and ZZ cohorts. Aluminum and iron concentrations were observed to increase in ZZ individuals relative to those with MM and MZ genotype (A). In contrast, copper levels decreased in both MZ and ZZ cohorts (A). Only the correlation between A1AT and iron concentration was significant (B).

Notes: *Significantly increased relative to the comparable sex-specific group of MM; **significantly decreased relative to the comparable sex-specific group of MM.

Abbreviation: A1AT, α-1 antitrypsin.

Discussion

Ferritin is considered the best available index to measure total body stores of iron.20–22 Significant differences in plasma ferritin concentrations between MM and ZZ individuals support an impact of A1AT deficiency on iron homeostasis in humans. Similarly, plasma iron levels were increased in the ZZ genotype. While the MZ genotype decreased A1AT levels, it did not influence ferritin and iron concentrations; this may reflect either a true lack of effect of A1AT genotype on iron homeostasis or the sample number may have been insufficient to demonstrate a difference. The significant correlations between both plasma levels of ferritin and iron with A1AT also suggest a participation of this anti-protease in iron homeostasis. A relationship between A1AT and ferritin can possibly be predicted since both would increase with inflammation. However, CRP levels were not significantly different between genotypes (MM, MZ, and ZZ) and there was no significant relationship between CRP and ferritin suggesting the increase in ferritin levels among ZZ individuals was not the result of disparities in inflammatory status. In addition, while both A1AT and ferritin are positive acute phase reactants, the relationship between them in our study cohort was an inverse one; that is, as A1AT decreased, ferritin increased. It is not possible to argue that inflammation is responsible for an increase in one index while the other is decreased.

This investigation does not address the molecular basis for a disruption in iron homeostasis in patients with A1AT deficiency. Proteases are employed as a third pathway of iron acquisition by microbials (in addition to siderophores and ferrireductases).23,24 These proteins have a capacity to cleave iron-transport and -storage proteins thus allowing utilization of the metal by the microbe.25–27 Reflecting potential interactions between metal availability and proteases, increased iron concentrations can impact expression and/or activity of collagenase, elastase, alkaline proteinase, and metalloproteases.9,10,12,28,29 In addition, in vitro exposure to the protease inhibitor A1AT alters iron homeostasis in eukaryotic cells.30–34 This serpin, which primarily inhibits neutrophil elastase, can elevate intracellular ferritin concentrations in cultured cells. In vivo exposure to protease disrupted iron homeostasis in an animal model.17 Finally, among patients with A1AT deficiency, iron homeostasis is disrupted.16,35,36 Accordingly, one mechanism through which A1AT deficiency can affect a disruption in iron homeostasis is by allowing an unrestricted activity of specific proteases which would result in increased iron availability. This will lead to elevated tissue concentrations of iron especially in the liver and spleen, which are major cites of storage. Reflecting this, blood ferritin will be increased among individuals with A1AT deficiency.

This disruption in iron homeostasis associated with A1AT deficiency can assist in understanding the clinical presentation of such patients. Clinical manifestations of A1AT deficiency most frequently include liver and lung disease. Liver tissue is one of the major sites for iron storage. With a lack of A1AT, there will be an accumulation of iron with subsequent elevations in liver concentrations. Elevated liver iron is associated with hepatitis, cirrhosis, and hepatocarcinoma, which are the manifestations of disease in A1AT deficiency among ZZ individuals. Inhaled exposures (eg, particles) precipitate a biological effect in the lung by disrupting the normal iron homeostasis and increasing the availability of host iron.37 Subsequently, particle exposure in A1AT deficient individuals is predicted to be associated with a higher incidence of disease (eg, chronic obstructive pulmonary disease among smokers and those exposed to elevated particle levels).38–40

We conclude that A1AT deficiency is associated with evidence of a disruption in iron homeostasis in ZZ individuals with plasma ferritin and iron concentrations being elevated. Such a disruption in iron homeostasis can contribute to understanding the clinical presentation of A1AT deficiency.