CoChat
Sign Up
Cited by 571Alzheimer's disease research and treatmentsMitochondrial Function and PathologyAutophagy in Disease and Therapy

The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.

Mitochondrial targeting and a novel transmembrane arrest of Alzheimer's amyloid precursor protein impairs mitochondrial function in neuronal cells

Open access
Anandatheerthavarada, Hindupur K., Biswas, Gopa, Robin, Marie-Anne, Avadhani, Narayan G.·2003·The Journal of Cell Biology
DOI 10.1083/jcb.200207030PMC PMC2172865
Open this paper in CoChat — free account

Abstract

Alzheimer's amyloid precursor protein 695 (APP) is a plasma membrane protein, which is known to be the source of the toxic amyloid beta (Abeta) peptide associated with the pathogenesis of Alzheimer's disease (AD). Here we demonstrate that by virtue of its chimeric NH2-terminal signal, APP is also targeted to mitochondria of cortical neuronal cells and select regions of the brain of a transgenic mouse model for AD. The positively charged residues at 40, 44, and 51 of APP are critical components of the mitochondrial-targeting signal. Chemical cross-linking together with immunoelectron microscopy show that the mitochondrial APP exists in NH2-terminal inside transmembrane orientation and in contact with mitochondrial translocase proteins. Mutational studies show that the acidic domain, which spans sequence 220-290 of APP, causes the transmembrane arrest with the COOH-terminal 73-kD portion of the protein facing the cytoplasmic side. Accumulation of full-length APP in the mitochondrial compartment in a transmembrane-arrested form, but not lacking the acidic domain, caused mitochondrial dysfunction and impaired energy metabolism. These results show, for the first time, that APP is targeted to neuronal mitochondria under some physiological and pathological conditions.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1083/jcb.200207030

Cites

47 of 47 references verified0 citation errors · 0 not checkable

Statistics

Figures

Figure 1. Chimeric signal properties of APP and its bimodal targeting to mitochondria and PMs. (A) Chimeric signals of APP and comparison with the signal domains of P4501A1 and 2B1. The ER-targeting sequence (1–36) of APP is indicated as a dark shaded area. Sequence 36–61 with three positively charged residues (at positions 40, 44, and 51), the predicted mitochondrial-targeting sequence, and the mutant construct 3M/APP carrying mutations at these positions are shown. (B) Immunoblot analysis of marker proteins for different subcellular fractions (50 μg protein each) using antibodies to Na+/K+ ATPase, TOM40, calreticulin, βCOP, and p97. The bottom panel represents 200 μg protein from each membrane fraction and was developed with APP Nt Ab. (C) Northern blot analysis of total RNA (25 μg RNA each) from HCN cells treated with PMA for different time intervals. Hybridization with 18S DNA probe served as a loading control. (D) Western blot analysis of mitochondria and PM proteins (200 μg protein each) from HCN cells treated with PMA for different time intervals using APP Nt Ab. (E) Measurement of reduction of MTT dye by freshly isolated mitochondria from HCN-1A cells treated with PMA for various time points was performed as described in the Materials and methods. (F) Immunoblot analysis of glycosidase-treated proteins (200 μg each) from PMA (100 nM)-induced HCN cells using APP Nt Ab. Treatment with glycosidases was performed as described in the Materials and methods. Mito, mitochondria.
Figure 1. Chimeric signal properties of APP and its bimodal targeting to mitochondria and PMs. (A) Chimeric signals of APP and comparison with the signal domains of P4501A1 and 2B1. The ER-targeting sequence (1–36) of APP is indicated as a dark shaded area. Sequence 36–61 with three positively charged residues (at positions 40, 44, and 51), the predicted mitochondrial-targeting sequence, and the mutant construct 3M/APP carrying mutations at these positions are shown. (B) Immunoblot analysis of marker proteins for different subcellular fractions (50 μg protein each) using antibodies to Na+/K+ ATPase, TOM40, calreticulin, βCOP, and p97. The bottom panel represents 200 μg protein from each membrane fraction and was developed with APP Nt Ab. (C) Northern blot analysis of total RNA (25 μg RNA each) from HCN cells treated with PMA for different time intervals. Hybridization with 18S DNA probe served as a loading control. (D) Western blot analysis of mitochondria and PM proteins (200 μg protein each) from HCN cells treated with PMA for different time intervals using APP Nt Ab. (E) Measurement of reduction of MTT dye by freshly isolated mitochondria from HCN-1A cells treated with PMA for various time points was performed as described in the Materials and methods. (F) Immunoblot analysis of glycosidase-treated proteins (200 μg each) from PMA (100 nM)-induced HCN cells using APP Nt Ab. Treatment with glycosidases was performed as described in the Materials and methods. Mito, mitochondria.CC BY-NC-SA · PubMed Central
Figure 2. Mitochondrial targeting of APP under in vitro and in vivo conditions. (A, B and C) WT/APP, 3M/APP, Δ220–290/APP, P450 MT2 (+33/1A1), and P450 MT4 (2B1) proteins were used for the in vitro transport in isolated rat brain mitochondria as described in the Materials and methods using 250 μg trypsin/ml of reaction (+). (A, lanes 4–6) Mitochondria were preincubated with or without added inhibitors (50 μM CCCP or 50 μM 2,4 DNP) at 25°C for 10 min before initiating the in vitro transport. (C) Mitochondria were treated with 0.1% Triton X-100 before treatment with trypsin. In each case, 200 μg of mitochondrial protein was used for electrophoresis, and the gels were subjected to fluorography. (D–G) In vivo targeting of WT/APP, 3M/APP, and Δ220–290/APP. HCN-1A cells were transfected with WT/APP (D and G), 3M/APP (E), and Δ220–290/APP (F) cDNA constructs, and PM and mitochondrial fractions were probed with APP Ct Ab (D–F) and APP Nt Ab (G). Trypsin treatment was performed as in A. Treatment with digitonin and extraction with 0.1 M Na2CO3 (D, lanes 9 and 10) were performed as described in the Materials and methods. P, pellet; S, supernatant.
Figure 2. Mitochondrial targeting of APP under in vitro and in vivo conditions. (A, B and C) WT/APP, 3M/APP, Δ220–290/APP, P450 MT2 (+33/1A1), and P450 MT4 (2B1) proteins were used for the in vitro transport in isolated rat brain mitochondria as described in the Materials and methods using 250 μg trypsin/ml of reaction (+). (A, lanes 4–6) Mitochondria were preincubated with or without added inhibitors (50 μM CCCP or 50 μM 2,4 DNP) at 25°C for 10 min before initiating the in vitro transport. (C) Mitochondria were treated with 0.1% Triton X-100 before treatment with trypsin. In each case, 200 μg of mitochondrial protein was used for electrophoresis, and the gels were subjected to fluorography. (D–G) In vivo targeting of WT/APP, 3M/APP, and Δ220–290/APP. HCN-1A cells were transfected with WT/APP (D and G), 3M/APP (E), and Δ220–290/APP (F) cDNA constructs, and PM and mitochondrial fractions were probed with APP Ct Ab (D–F) and APP Nt Ab (G). Trypsin treatment was performed as in A. Treatment with digitonin and extraction with 0.1 M Na2CO3 (D, lanes 9 and 10) were performed as described in the Materials and methods. P, pellet; S, supernatant.CC BY-NC-SA · PubMed Central
Figure 3. Subcellular localization of WT/APP and 3M/APP by immunofluorescence microscopy. HCN-1A cells (A–L) and COS cells (M–R) were transfected with WT/APP (A–F) or 3M/APP (G–L). The inset in F is a twofold enlargement of a region showing APP Ab–stained granular structures both overlapping and nonoverlapping with mitochondrial stain, as indicated by arrows. Nonpermeabilized cells (A–C, G–I, and M–O) were double immunostained with APP Nt Ab and monoclonal antibody to Na+/ K+ ATPase. Permeabilized cells (D–F, J–L, and P–R) were double stained with APP Nt Ab and rabbit polyclonal antibodies to TOM40. Staining patterns (A, B, D, E, G, H, J, K, M, N, P, and Q) were developed with appropriate secondary antibodies conjugated to Alexa dyes. (C, F, I, L, O, and R) Respective overlay patterns.
Figure 3. Subcellular localization of WT/APP and 3M/APP by immunofluorescence microscopy. HCN-1A cells (A–L) and COS cells (M–R) were transfected with WT/APP (A–F) or 3M/APP (G–L). The inset in F is a twofold enlargement of a region showing APP Ab–stained granular structures both overlapping and nonoverlapping with mitochondrial stain, as indicated by arrows. Nonpermeabilized cells (A–C, G–I, and M–O) were double immunostained with APP Nt Ab and monoclonal antibody to Na+/ K+ ATPase. Permeabilized cells (D–F, J–L, and P–R) were double stained with APP Nt Ab and rabbit polyclonal antibodies to TOM40. Staining patterns (A, B, D, E, G, H, J, K, M, N, P, and Q) were developed with appropriate secondary antibodies conjugated to Alexa dyes. (C, F, I, L, O, and R) Respective overlay patterns.CC BY-NC-SA · PubMed Central
Figure 4. Transmembrane-arrested APP exists in contact with mitochondrial translocase proteins. 35S-labeled APP (1–220) fused to DHFR (APP–DHFR), WT/APP, or Δ220–290/APP proteins were used for in vitro transport with isolated yeast mitochondria, and translocation intermediates were cross-linked with MBS as described below. In indicated experiments, MTX (1 μmol/ml of reaction) was added to generate translocation intermediates. Both the input and cross-linked products were immunoprecipitated with antibody to APP and then probed with indicated antibodies by immunoblot analysis. (A) In vitro transport of APP–DHFR fusion protein. Trypsin treatment (250 μg /ml reaction) was performed for 20 min on ice as described in the Materials and methods. (B) Cross-linking of APP–DHFR fusion protein with yeast mitochondrial translocases. (C) Cross-linking of WT/APP and Δ220–290/APP with yeast mitochondrial translocase proteins. In vitro transport was performed with indicated proteins in the absence of added MTX. (D, E, and F) Immunoelectron microscopy of HCN-1A cells transfected with WT/APP, 3MAPP, and Δ22–290/APP, respectively, for 32 h. M, mitochondrion; G, Golgi; E, ER; N, nucleus; V, vesicles. Arrow 1, COOH terminus of APP (10-nm gold particle); arrow 2, TOM40 (20-nm gold particle); arrow 3, NH2 terminus of APP (5-nm gold particle).
Figure 4. Transmembrane-arrested APP exists in contact with mitochondrial translocase proteins. 35S-labeled APP (1–220) fused to DHFR (APP–DHFR), WT/APP, or Δ220–290/APP proteins were used for in vitro transport with isolated yeast mitochondria, and translocation intermediates were cross-linked with MBS as described below. In indicated experiments, MTX (1 μmol/ml of reaction) was added to generate translocation intermediates. Both the input and cross-linked products were immunoprecipitated with antibody to APP and then probed with indicated antibodies by immunoblot analysis. (A) In vitro transport of APP–DHFR fusion protein. Trypsin treatment (250 μg /ml reaction) was performed for 20 min on ice as described in the Materials and methods. (B) Cross-linking of APP–DHFR fusion protein with yeast mitochondrial translocases. (C) Cross-linking of WT/APP and Δ220–290/APP with yeast mitochondrial translocase proteins. In vitro transport was performed with indicated proteins in the absence of added MTX. (D, E, and F) Immunoelectron microscopy of HCN-1A cells transfected with WT/APP, 3MAPP, and Δ22–290/APP, respectively, for 32 h. M, mitochondrion; G, Golgi; E, ER; N, nucleus; V, vesicles. Arrow 1, COOH terminus of APP (10-nm gold particle); arrow 2, TOM40 (20-nm gold particle); arrow 3, NH2 terminus of APP (5-nm gold particle).CC BY-NC-SA · PubMed Central
Figure 5. Subcellular distribution of ectopically expressed APPs in HCN-1A cells. Cells were transfected with WT/APP (A–D), 3M/APP (E–H), Δ220–290/APP (I–L), and SW/APP (M–P). At indicated times after transfection, mitochondria (MITO.), PM, and Golgi fractions (50 μg protein each) and also protein concentrate from 10 ml of cell-free culture medium (CM) were subjected to Western immunoblot analysis using antibodies to APP Nt (A, B, E, F, I, J, M, and N) or Aβ (C, D, G, H, K, L, O, and P). (Q) The level of expression of total APP protein in cells transfected with various cDNA constructs for different time points was monitored by immunoblot analysis of whole cell lysates. The antibody-reactive proteins were quantified using a Bio-Rad Laboratories Fluoro S imaging system. Table I shows the distribution of APP in different membrane fractions at different time points after transfection with WT/APP and SW/APP cDNAs. Values at the bottom of Q show relative APP levels in comparison with the level at 24-h transfection that was considered to be 1. (R) Pulse chase characteristics of mitochondrial- and PM-associated APP. HCN-1A cells transfected with WT/APP cDNA for 24 h were labeled with [35S]Met for 2 h, followed by a chase in normal growth medium containing 3 mM unlabeled Met. Mitochondrial and PM proteins from cells at different points of chase (500 μg each) were immunoprecipitated with APP Nt Ab, analyzed by electrophoresis on 10% SDS-polyacrylamide gels, and imaged through a Bio-Rad Laboratories GS525 molecular imager. The immunoblot at the top of the figure was performed using 100 μg protein from each fraction using APP Nt Ab.
Figure 5. Subcellular distribution of ectopically expressed APPs in HCN-1A cells. Cells were transfected with WT/APP (A–D), 3M/APP (E–H), Δ220–290/APP (I–L), and SW/APP (M–P). At indicated times after transfection, mitochondria (MITO.), PM, and Golgi fractions (50 μg protein each) and also protein concentrate from 10 ml of cell-free culture medium (CM) were subjected to Western immunoblot analysis using antibodies to APP Nt (A, B, E, F, I, J, M, and N) or Aβ (C, D, G, H, K, L, O, and P). (Q) The level of expression of total APP protein in cells transfected with various cDNA constructs for different time points was monitored by immunoblot analysis of whole cell lysates. The antibody-reactive proteins were quantified using a Bio-Rad Laboratories Fluoro S imaging system. Table I shows the distribution of APP in different membrane fractions at different time points after transfection with WT/APP and SW/APP cDNAs. Values at the bottom of Q show relative APP levels in comparison with the level at 24-h transfection that was considered to be 1. (R) Pulse chase characteristics of mitochondrial- and PM-associated APP. HCN-1A cells transfected with WT/APP cDNA for 24 h were labeled with [35S]Met for 2 h, followed by a chase in normal growth medium containing 3 mM unlabeled Met. Mitochondrial and PM proteins from cells at different points of chase (500 μg each) were immunoprecipitated with APP Nt Ab, analyzed by electrophoresis on 10% SDS-polyacrylamide gels, and imaged through a Bio-Rad Laboratories GS525 molecular imager. The immunoblot at the top of the figure was performed using 100 μg protein from each fraction using APP Nt Ab.CC BY-NC-SA · PubMed Central
Figure 6. Effects of transmembrane-arrested APP on mitochondrial functions. Total cell extracts or mitochondria from HCN-1A cells transfected with WT/APP, 3M/APP, Δ220–290/APP, and SW/APP were analyzed for CytOX activity (A), mitochondria and total cell ATP generation (B and C, respectively), and changes in the mitochondrial membrane potential using MitoTracker orange CM-H2TM ROS (D), as described in the Materials and methods. Mitochondrial CytOX activity (2 nmol of cytochrome c oxidized/min/mg mitochondrial protein) from vector alone–transfected cells was used as 100% activity. Values represent mean ± SEM from three separate transfection experiments.
Figure 6. Effects of transmembrane-arrested APP on mitochondrial functions. Total cell extracts or mitochondria from HCN-1A cells transfected with WT/APP, 3M/APP, Δ220–290/APP, and SW/APP were analyzed for CytOX activity (A), mitochondria and total cell ATP generation (B and C, respectively), and changes in the mitochondrial membrane potential using MitoTracker orange CM-H2TM ROS (D), as described in the Materials and methods. Mitochondrial CytOX activity (2 nmol of cytochrome c oxidized/min/mg mitochondrial protein) from vector alone–transfected cells was used as 100% activity. Values represent mean ± SEM from three separate transfection experiments.CC BY-NC-SA · PubMed Central
Figure 7. Mitochondrial-associated APP in the brains of transgenic mice overexpressing APP. (A) Mitochondria and PM fractions from different brain regions of control and SWEAPP (2576) transgenic mice (50 μg protein each) were subjected to immunoblot analysis using APP Nt Ab. (B) Mitochondria (50 μg) from different brain regions of transgenic mice overexpressing SW/APP (SWEAPP [2576]) were subjected to trypsin treatment (as described in Fig. 2) followed by immunoblot analysis with APP Nt Ab. (C) CytOX activity in total mitochondrial membrane fraction and (D) total cellular ATP levels were assayed as described in the Materials and methods. MITO., mitochondria; Ctl, control; Tg, transgenic; Ct, cortex; Hp, hippocampus; Ce, cerebellum.
Figure 7. Mitochondrial-associated APP in the brains of transgenic mice overexpressing APP. (A) Mitochondria and PM fractions from different brain regions of control and SWEAPP (2576) transgenic mice (50 μg protein each) were subjected to immunoblot analysis using APP Nt Ab. (B) Mitochondria (50 μg) from different brain regions of transgenic mice overexpressing SW/APP (SWEAPP [2576]) were subjected to trypsin treatment (as described in Fig. 2) followed by immunoblot analysis with APP Nt Ab. (C) CytOX activity in total mitochondrial membrane fraction and (D) total cellular ATP levels were assayed as described in the Materials and methods. MITO., mitochondria; Ctl, control; Tg, transgenic; Ct, cortex; Hp, hippocampus; Ce, cerebellum.CC BY-NC-SA · PubMed Central
Figure 8. A proposed model for the mitochondrial targeting and accumulation of transmembrane- arrested APP affecting mitochondrial functions.
Figure 8. A proposed model for the mitochondrial targeting and accumulation of transmembrane- arrested APP affecting mitochondrial functions.CC BY-NC-SA · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 47 references

Research works printed but not linked: 1

  1. 1996, Int. J. Dev. Neurosci., 14, 61

Cited by

Sorted by citations

Items 401–500 of 570

Related

See all

Metadata

Authors
Anandatheerthavarada, H. K., Biswas, G., Robin, M.-A., & Avadhani, N. G.
Affiliations
University of Pennsylvania (US)
ORCID
Avadhani, Narayan G.
Venue
The Journal of Cell Biology
Publisher
Rockefeller University Press
Published
2003-04-14
Volume
161
Issue
1
Pages
41-54
ISSN
  • 0021-9525 (ISSN-L)
  • 1540-8140
DOI
10.1083/jcb.200207030
PMC
PMC2172865
OpenAlex
W2132988134
Cited by
571
References
47
Citations by year
2026: 11 · 2025: 12 · 2024: 18 · 2023: 22 · 2022: 16 · 2021: 24 · 2020: 23 · 2019: 18 · 2018: 35 · 2017: 14 · 2016: 27 · 2015: 24 · 2014: 17 · 2013: 24 · 2012: 31
FWCI
13.60
Type
journal article
Language
en
Open access
Licence
cc-by-nc-sa
Locations
  • The Journal of Cell Biology (publishedVersion)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (1r01gm034483-01a3)
  • National Institute of General Medical Sciences (GM34483)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
Keywords
amyloid precursor protein, APP695, mitochondrial targeting, mitochondrial dysfunction, energy metabolism, Alzheimer's disease, amyloid-beta, mitochondrial translocase, acidic domain, cortical neurons, transgenic mouse model, crosslinking, immunoelectron microscopy
MeSH terms
Alzheimer Disease, Amino Acid Sequence, Animals, Brain, Cell Compartmentation, Cells, Cultured, Disease Models, Animal, Energy Metabolism, Humans, Immunohistochemistry, Intracellular Membranes, Mice, Transgenic, Microscopy, Electron, Mitochondria, Molecular Conformation, Neurons, Recombinant Fusion Proteins, Amyloid beta-Protein Precursor, Protein Structure, Tertiary, Protein Transport, Cytochrome-c Oxidase Deficiency, Mice

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review