Chronic early life lead (Pb2+) exposure alters presynaptic vesicle pools in hippocampal synapses
© The Author(s). 2016
Received: 1 June 2016
Accepted: 14 October 2016
Published: 2 November 2016
Lead (Pb2+) exposure has been shown to impair presynaptic neurotransmitter release in both in vivo and in vitro model systems. The mechanism by which Pb2+ impairs neurotransmitter release has not been fully elucidated. In previous work, we have shown that Pb2+ exposure inhibits vesicular release and reduces the number of fast-releasing sites in cultured hippocampal neurons. We have also shown that Pb2+ exposure inhibits vesicular release and alters the distribution of presynaptic vesicles in Shaffer Collateral – CA1 synapses of rodents chronically exposed to Pb2+ during development.
In the present study, we used transmission electron microscopy to examine presynaptic vesicle pools in Mossy Fiber-CA3 synapses and in Perforant Path-Dentate Gyrus synapses of rats to determine if in vivo Pb2+ exposure altered presynaptic vesicle distribution in these hippocampal regions. Data were analyzed using T-test for each experimental endpoint.
We found that Pb2+ exposure significantly reduced the number of vesicles in the readily releasable pool and recycling pool in Mossy Fiber-CA3 terminals. In both Mossy Fiber-CA3 terminals and in Perforant Path-Dentate Gyrus terminals, Pb2+ exposure significantly increased vesicle nearest neighbor distance in all vesicular pools (Rapidly Releasable, Recycling and Resting). We also found a reduction in the size of the postsynaptic densities of CA3 dendrites in the Pb2+ exposed group.
In our previous work, we have demonstrated that Pb2+ exposure impairs vesicular release in Shaffer Collateral - CA1 terminals of the hippocampus and that the number of docked vesicles in the presynaptic active zone was reduced. Our current data shows that Pb2+ exposure reduces the number of vesicles that are in proximity to release sites in Mossy Fiber- CA3 terminals. Furthermore, Pb2+ exposure causes presynaptic vesicles to be further from one another, in both Mossy Fiber- CA3 terminals and in Perforant Pathway – Dentate Gyrus terminals, which may interfere with vesicle movement and release. Our findings provide a novel in vivo mechanism by which Pb2+ exposure impairs vesicle dynamics and release in the hippocampus.
KeywordsLead (Pb2+) Synapses Presynaptic Vesicles Postsynaptic Density (PSD) Mitochondria
Effective neurotransmission requires appropriate expression, packaging, release, reception and degradation or reuptake of neurotransmitters . Mechanisms underlying the release of neurotransmitters are highly complex and require precise interactions between pre-synaptic membrane proteins, vesicular proteins, ions and energy . Exposure to lead (Pb2+) has been shown to inhibit the release of neurotransmitters, including glutamate and γ-aminobutyric acid (GABA), in various in vivo, in vitro and ex vivo models [3–6].
It is well known that the brain is a primary target of Pb2+ toxicity [7, 8]. Pb2+ can readily cross the blood brain barrier (BBB), and is found in brain homogenate following Pb2+ exposure , which is likely due to the ability of Pb2+ to substitute for Ca2+ ions [10, 11]. On the cellular level, Pb2+ exposure results in a myriad of direct effects in brain, which include apoptosis, excitotoxicity and alterations in neurotransmitter storage and release [12–20].
The mechanism by which Pb2+ exposure impairs vesicular release appears to involve presynaptic releasing sites [18–20]. In hippocampal neuron cultures, we have shown that Pb2+ exposure increased the number of nascent presynaptic contact sites. These release sites may be immature and lack the necessary vesicular release machinery proteins, thus contributing to reduced vesicular docking and release . The mechanism by which Pb2+ exposure decreases the number of vesicular docking sites may involve retrograde Brain Derived Neurotrophic Factor (BDNF) – Receptor Tyrosine Kinase B (TrkB) receptor signaling . Pb2+ is a potent inhibitor of the N-Methyl-d-Aspartate (NMDA) receptor, [21–23] whose activation is essential for cAMP Response Element (CREB) phosphorylation and subsequent BDNF expression . Inhibition of the NMDA receptor by Pb2+ exposure reduces the expression of BDNF and impairs presynaptic BDNF-TrkB receptor signaling [5, 18, 19]. Reduced BDNF-TrkB interaction on presynaptic sites decreases the phosphorylation of synapsin-1, a vesicular protein which is important in vesicle-synaptic membrane interactions and is imperative to vesicular release [23–25]. Previously, we have shown that synapsin I phosphorylation at sites 4 (serine 62) and 5 (serine 67) were significantly decreased by Pb2+ exposure with no effect on total synapsin I protein levels . The effect of Pb2+ on these particular signaling mechanisms is not reversed when Pb2+ is removed from the system which suggests that Pb2+ exposure results in persistent, deleterious effects on neurotransmission. On the other hand, the inhibitory effect of Pb2+ on L-type calcium channels can be reversed with removal of Pb2+ . Therefore, the permanent effect of Pb2+ exposure on vesicular exocytotic mechanisms appears to be exceedingly important in Pb2+ exposure induced deficits in neurotransmission.
Mechanistic studies demonstrate that Pb2+ can have an effect on multiple cellular constituents that are involved in neurotransmission, thus leading to differential effects of Pb2+ exposure on neurotransmission in different brain regions, even within the same structure. For example, chronic, low-level exposure to lead has been shown to reduce long term potentiation (LTP) in NMDA receptor-dependent CA1 synapses, while having no effect on LTP in NMDA receptor - independent synapses of the CA3 region of the hippocampus . Recently, we have shown that Pb2+ markedly inhibits presynaptic vesicular release in the hippocampal Shaffer Collateral – CA1 synapses in young adult rats. In support of previous data, impairments in vesicular release were found in CA1 but not in CA3 immediately following stimulation. This decrease in vesicular release in CA1 was found along with a decrease in both the rapidly releasable pool/docked (RRP/docked) vesicle pools as well as the recycling pool of vesicles, with no overall reduction in the total number of presynaptic vesicles. Furthermore, vesicles in the Pb2+ exposure group were further apart from one another, irrespective of the distance of the vesicle to the presynaptic active zone (PAZ). Interestingly, at later time points, impairments in vesicular release became apparent in the CA3, demonstrating the differential effects of Pb2+ on neurotransmission in the CA1 and CA3 brain regions .
Mitochondria are organelles that are intricately involved in neurotransmission, as they provide energy for vesicular biogenesis, packaging, movement and release . Mitochondria are typically synthesized in the cell body, are sent to the axonal terminal for energy and then sent back to the cell body for degradation . Exposure to Pb2+ has been shown to have numerous detrimental effects on mitochondria [30–32]. Our previous work has shown that chronic Pb2+ exposure reduces the number of mitochondria found in Shaffer Collateral- CA1 synapses . Mechanistically, Pb2+ exposure can impair ATP synthesis, which would in turn limit energy-expending activities. Therefore, the effect of Pb2+ on presynaptic mitochondria may contribute to impaired vesicular release.
In light of our previous work, which demonstrated that there was a latent but significantly impaired neurotransmission in the CA3 following Pb2+ exposure, we sought to determine if Pb2+ exposure could affect the distribution of vesicular pools in the presynaptic terminals of asymmetric Mossy Fiber-CA3 synapses, using electron microscopy. We also examined the effect of Pb2+ exposure on asymmetric Perforant Pathway-Dentate Gyrus synapses, another region of the hippocampus in which Pb2+ exposure has been shown to impair long term potentiation . Asymmetric synapses can be identified using electron microscopy by identification of the postsynaptic density (PSD). We have selected to examine the synapses of rats exposed to 1500 ppm lead. Feeding rats this concentration of lead yields a blood lead level of approximately 21 ug/dL. Previous studies have shown that a BLL of approximately 27 ug/dL yields a significant change in NMDA receptor expression as compared to low level Pb2+ exposure and highly concentrated Pb2+ exposure . Since we examined asymmetric synapses via identification of the PSD, which typically contain NMDA receptors, we thought that a creating a model with a BLL comparable to that which produces Pb2+ mediated effects on NMDA receptor would allow us to characterize the maximal effect of Pb2+ on vesicular pools. Furthermore, we have found that this particular exposure produced profound spatial learning deficits [6, 34], which likely reflect the effect of this particular concentration of Pb2+ on hippocampal function. Additionally, we studied the number and size of mitochondria in the presynaptic terminals to determine if there were changes in mitochondrial size, number and distribution that could affect energy availability in the presynaptic terminals and examined the size of the postsynaptic density in asymmetrical synapses.
All chemicals used for electron microscopy (Glutaraldehyde, Paraformaldehyde, Osmium Tetroxide, Uranyl Acetate, Ethanol, Propylene Oxide and Spurr’s Low Viscosity Resin Embedding Kit) were purchased from Electron Microscopy Sciences (Hatfield, PA, USA).
Adult female Long-Evans rats were purchased from Charles River, Inc. (Wilmington, MA) and fed 0 (control) or 1500 ppm lead acetate (PbAc) in the diet (Dyets, Bethlehem, PA) 10 days prior to breeding with normal Long-Evans males. Litters were culled to 10 on postnatal day 1 (PN1). Dams were maintained on their respective diet until weaning of pups. After weaning, offspring remained on respective maternal diet until PN 50. Rats were housed in pairs in rectangular plastic cages at 22 ± 2 °C on a 12/12 light:dark cycle. Food and water were allowed ad libitum. Rats were provided with corn cob bedding which was changed on a weekly basis. 10 litters of rats were bred for these studies. We used a litter based design in which one male rat per litter was randomly selected for inclusion into either the control group or the control group (n = 10, n = 5 Pb2+; n = 5 control). The number of animals to be used was calculated with a Power Analysis using G*Power 3.1 statistical software. This study was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was approved by Columbia University Institutional Animal Care and Use Committees (AC-AAAF4810). All non-survival procedures were performed under sodium pentobarbital anesthesia, and all efforts were made to minimize suffering.
All perfusion procedures were carried out during the light cycle (1300–1600 h). At PN 50, Long-Evans male rats were anesthetized with 20 mg/kg pentobarbital via intraperitoneal injection in their home cage. Pentobarbital was selected because it acts upon the GABAA receptor to induce anesthesia. Blood was transcardially perfused with 2.5 % Glutaraldehyde + 2 % Paraformaldehyde in 0.1 M Phosphate Buffered Saline (PBS). The brain was removed and post-fixed in the same solution overnight at room temperature (RT). Brains were sectioned into 500 um slices with a vibratome. Sections were laid flat and two regions of interest (Perforant Pathway – Dentate Gyrus synapses and Mossy Fiber – CA3 synapses) were dissected from the right hippocampus using a hole-punch method (Fig. 2). The right side of the brain is typically associated with visuospatial processing and spatial memory . Since Pb2+ exposure results in decreased spatial learning ability, we chose to investigate the right hippocampus because it isassociated with spatial learning [6, 34]. Male rats, in particular, exhibit prominent laterality . Dissected tissue was placed in the 2.5 % Glutaraldehyde + 2 % Paraformaldehyde in PBS mixture for 3 additional h at RT and rinsed with PBS. Secondary fixation in 1 % osmium tetraoxide in PBS was then done for 60 m at RT. Following osmium fixation, tissue was rinsed in PBS then rinsed in water to remove all traces of phosphate from samples. Tissue was subsequently dehydrated in 50 % ethanol, a mixture of 70 % ethanol + 1 % uranyl acetate, 85 % ethanol and 2 changes of 100 % ethanol (15 m per step). Tissue was then placed in the transition solvent propylene oxide twice (15 m per step) and was left to infiltrate in a 1:1 mixture of propylene oxide-Spurr’s Resin overnight at RT. Steps involving osmium tetraoxide and uranyl acetate were done in containers covered with foil to block light. Tissue was transferred to pure Spurr’s Resin for infiltration for 24 h at RT. Tissue was then placed into Beem Capsules with fresh Spurr’s Resin, allowed to sit for 30 m and then placed in a 70 C oven for 24 h for polymerization. After polymerization, ultrathin sections (70 nm) were obtained using a Leica Ultracut ultramicrotome and placed onto 200 mesh copper grids. 2 um of tissue was cut in between each collected section to prevent repeat analysis of any synapses. Sections on grids were then stained with uranyl acetate for 45 m, rinsed with water, stained with lead citrate for 90 s, rinsed with water and left to dry on clean filter paper.
To obtain the appropriate number of images for these analyses, we calculated the number of images needed using G*Power statistical software. 40 images of the Mossy Fiber - CA3 synapses were needed for each rat. We then made 17 measurements per image. Each measurement reflected a single experimental endpoint under investigation (ex. Docked vesicle number, PSD length, number of mitochondria in terminals, etc). We then used the 40 images to obtain the mean measurement for each of the experimental endpoints per rat. This led to the generation of 10 mean values for each experimental endpoint under investigation (ex. 5 Control means vs. 5 Pb2+ means for the Mossy Fiber - CA3 synapses per endpoint). We used a T-test to compare the mean values of the Control vs. Pb2+ exposed groups to determine if there were differences in the particular endpoint being investigated (GraphPad Prism). Data is reported as SEM, as we were examining differences between the means of each experimental group . We also analyzed the same endpoints in the Perforant Pathway - DG synapses, a functionally distinct part of the hippocampus, using the same strategy. Differences were considered significant if p < 0.05.
Blood Lead Level (BLL) and weight
The Pb2+ exposure paradigm used in the present study does not produce any overt toxicity based on body weight gain. Body weight at postnatal day 50 (PN50) were: 294.4 ± 4.8 grams (n = 24) for control animals and 281.6 ± 6.9 grams for Pb2+ -exposed animals. Blood Pb2+ levels of littermates to animals used in this study at PN50 were: 0.8 ± 0.3 μg/dL (n = 11) for control animals and 21.1 ± 1.6 μg/dL (n = 15) for Pb2+-exposed animals.
Analysis of vesicle number
Vesicle, clustering, and mitochondrial measurements in Dentate Gyrus –Perforant Pathway (DG-PP) synapses and CA3-Mossy Fiber Pathway (CA3-MF) Synapses
CA3 – Mossy Fiber Terminals
Dentate Gyrus – Perforant Pathway Terminals
Control (Mean ± SEM)
Pb2+ (Mean ± SEM)
Control (Mean ± SEM)
Pb2+ (Mean ± SEM)
I. Raw Vesicle Counts
A) Rapidly Releasable/Docked Vesicle Pool
8.527 ± 0.8456
6.018 ± 0.001
7.013 ± 1.003
5.232 ± 0.9928
B) Recycling Vesicle Pool
35.19 ± 7.804
29.26 ± 7.381
31.48 ± 9.315
26.09 ± 5.835
C) Resting Vesicle Pool
43.64 ± 5.570
51.80 ± 7.427
51.66 ± 8.374
59.80 ± 11.44
D) Total Number of Vesicles
87.36 ± 10.61
87.17 ± 1.761
90.07 ± 9.363
91.12 ± 10.46
II. Vesicular Diameters
A) Rapidly Releasable/Docked Diameter
20.67 ± 1.644
21.20 ± 1.137
20.82 ± 1.521
23.27 ± 2.12
B) Recycling Vesicle Diameter
22.09 ± 0.8383
22.77 ± 0.6942
22.10 ± 0.8234
24.41 ± 2.072
C) Resting Vesicle Diameter
24.83 ± 1.746
24.70 ± 1.322
24.69 ± 2.481
26.28 ± 2.506
D) Average Diameter of all vesicles
23.77 ± 1.406
23.84 ± 0.8775
23.72 ± 1.565
25.64 ± 2.094
III. Length Measurements
A) PSD length
309.1 ± 13.48
259.7 ± 18.74
269.3 ± 9.680
266.6 ± 15.31
B) PAZ length
311.6 ± 11.15
281.2 ± 19.53
265.6 ± 14.45
308.2 ± 26.90
IV. Nearest Neighbor Distance (Clustering)
A) Rapidly Releasable/Docked + Recycling (0–200 nm)
40.19 ± 1.398
45.56 ± 1.498
41.75 ± 0.7873
48.57 ± 1.115
B) Resting (201–500 nm)
42.04 ± 1.834
48.47 ± 1.157
45.35 ± 0.7979
51.19 ± 0.7168
V. Mitochondrial Measurements
A) Terminals with mitochondria
15.40 ± 2.227
17.60 ± 1.806
27.00 ± 3.050
22.60 ± 3.280
B) Terminals with multiple mitochondria
2.00 ± 0.5477
1.250 ± 0.2500
4.200 ± 0.9695
2.600 ± 0.5099
C) Total number of mitochondria
48.60 ± 6.577
54.20 ± 7.690
69.60 ± 0.4964
62.80 ± 0.2518
D) Diameter of mitochondria
231.6 ± 16.18
224.4 ± 15.53
221.8 ± 0.8072
226.5 ± 8.529
E) Large mitochondria (300 nm or greater)
4.800 ± 1.594
6.800 ± 0.9695
8.00 ± 2.345
7.200 ± 1.530
We also measured postsynaptic density (PSD) and presynaptic active zone (PAZ) length in Mossy Fiber-CA3 and Perforant Path-Dentate Gyrus synapses. We found that PSD length in CA3 dendrites was significantly reduced in rats chronically exposed to Pb2+ (p = 0.0382; Table 1 , IIIA). There was no change in Dentate Gyrus dendrites (p = 0.4432; Table 1 , IIIA). PAZ length was similar in the dendridic fields of the control and Pb2+ exposed rats (p = 0.0899 and p = 0.1553, respectively; Table 1 , IIIB). The reduction in the RRP/docked vesicle pool may contribute to the reduced size of the PSD that was found in the striatum radiatum of CA3 dendrites.
Vesicle clustering (nearest neighbor distance)
A reduction in vesicle clustering was the most ubiquitous effect of chronic Pb2+ exposure. Vesicles were more dispersed in Pb2+ exposed animals relative to controls in both Mossy Fiber and Perforant Pathway terminals. For example, the nearest neighbor distance in vesicles that are within 200 nm of the PAZ in both the Mossy Fiber and the Perforant Path were significantly greater in Pb2+ exposed animals as compared to controls (p = 0.0062 and 0.0001, respectively; Table 1 , IVA). Similarly, nearest neighbor distance of vesicles in the resting pool (greater than 200 nm from the PAZ) are also less clustered in Mossy Fiber and Perforant Pathway axon terminals from Pb2+ exposed animals as compared to controls (p = 0.0020 and 0.0001, respectively; Table 1 , IVB).
Chronic Pb2+ exposure did not result in any remarkable changes in mitochondria number or size. In the Pb2+ exposure group, there are no differences in the total number of terminals with mitochondria (p = 0.2340 and p = 0.1793, respectively, Table 1 , VA). In Pb2+ exposed rats, there is a modest reduction in Perforant Pathway terminals that contained multiple mitochondria, but the difference did not reach statistical significance (p = 0.0970, respectively; Table 1 , VB). The mean number of total mitochondria in both Mossy Fiber and Perforant Pathway terminals were not significantly different from controls (p = 0.5972 and p = 0.1375, respectively; Table 1 , VC). The mean diameter of Mossy Fiber and Perforant Pathway terminal mitochondria was similar between control and Pb2+ exposed groups (p = 0.7566 and p = 0.3500, respectively, Table 1 , VD). The number of mitochondria with a cross sectional diameter greater than 300 nm were not significantly between Pb2+ exposed groups and control groups in Mossy Fiber terminals or in Perforant Pathway Terminals (p = 0.1624 and p = 0.3924, respectively; Table 1 , VE).
The purpose of our work was to determine if Pb2+ effected the distribution of presynaptic vesicular pools, distribution of vesicles, and mitochondrial size in the Mossy Fiber – CA3 and Perforant Pathway – Dentate Gyrus terminals of the hippocampus of rats. Our work shows that Pb2+ exposure results in a decreased number of RRP/docked vesicles and recycling pool vesicles in Mossy Fiber – CA3 terminals. Pb2+ exposure did not alter vesicle number in the different pools of the Perforant Pathway – Dentate Gyrus terminals. Pb2+ treatment did not appear to affect the size of the vesicles or affect the biogenesis of the vesicles, as there were no differences in the total number of vesicles present in the terminals. Nearest neighbor distance of vesicles in both the Mossy Fiber – CA3 terminals and in Perforant Pathway – Dentate Gyrus terminals of Pb2+ exposed animals were significantly greater than controls, indicating that the vesicles were more dispersed in the Pb2+ exposed animals.
With respect to the RRP/docked vesicles, Pb2+ exposure consistently induced a significant reduction in the number of vesicles that were contacting the PAZ in Mossy Fiber terminals. In primary hippocampal culture, we found that Pb2+ exposure increased the number of nascent presynaptic docking sites, but many of these docking sites were lacking NSF attachment protein receptor complex, which is involved in vesicular exocytosis [5, 7]. It seems plausible that Pb2+ exposure may have a similar effect in vivo, which may contribute to the reduced number of RRP/docked vesicles that were found in the Pb2+-exposed animals. In our previous work, we found that Pb2+ exposure reduced the expression of synaptophysin and synaptobrevin, two vesicular proteins that are imperative to vesicular docking and release , which may contribute to the Pb2+ -induced changes that we have found in our current study.
We found fewer vesicles in the recycling pool of Pb2+ exposed animals, but no decrease in the total number of vesicles in each terminal. Pb2+ exposure also altered the distribution of the vesicles, as they were significantly further apart from one another in all hippocampal regions that were examined. Our data suggests that Pb2+ does not affect the biogenesis of the vesicles. The spatial arrangement of vesicles relative to the PAZ was highly affected by Pb2+ exposure, which likely reflects Pb2+ induced changes to the expression and activation of vesicular trafficking proteins and scaffolding proteins, such as synapsin. We have previously demonstrated that Pb2+ reduces phosphorylation of synapsin I in primary hippocampal culture. Synapsin I is a vesicular protein that in its unphosphorylated state keeps reserve pool vesicles bound to actin filaments. Once phosphorylated, vesicles are released from actin filaments and allowed to move into the recycling and RRP/docked vesicle pools [23–25]. We have shown that synapsin I phosphorylation at sites 4 (serine 62) and 5 (serine 67) were significantly decreased by Pb2+ exposure with no effect on total synapsin I protein levels . It is possible that Pb2+ reduces synapsin I phosphorylation in vivo as well, which may contribute to the decreased number of vesicles in the recycling and RRP/docked vesicle pools that we observed in the present study.
Mitochondria, which provide energy for vesicular biogenesis, were largely unaffected by Pb2+ exposure in the Mossy Fiber-CA3 and Perforant Path- Dentate Gyrus synapses. This suggests that Pb2+ exposure may not effect energy production in these terminal regions, which is supported by the idea that there does not appear to be any reduction in vesicular biogenesis, evidenced by no observable changes in presynaptic vesicle number or diameter. Interestingly, we did find that Pb2+ exposure did reduce the number of Shaffer-Collateral terminals with multiple mitochondria , demonstrating varying aberrant pathological effects in the different hippocampal regions. This study does not rule out the possibility of mitochondrial dysfunction, but from the measures that we investigated, there appear to be no gross ultrastructural differences. Mitochondrial cristae morphology may reveal differences in energy production and may be examined in future investigations.
The PSD length in CA3 dendrites was significantly reduced in Pb2+ exposed animals. Pb2+ exposure may impair the maturation of the PSD. PSD-95 expression enhances pre-synaptic maturation  thus a Pb2+ exposure-induced reduction of PSD size may contribute to the presynaptic changes that we observed. In previous work, we found that Pb2+ exposure results in a significant reduction in Timm’s-positive staining in Mossy Fibers terminal fields . Perhaps a reduction in the PSD in CA3 results in fewer axonal terminals that innervate this region. The length of the PSD in the dendrites of the Dentate Gyrus were not affected by Pb2+ exposure.
Chronic, early life Pb2+ exposure alters the distribution of vesicles in both Mossy Fiber and Perforant Pathway terminals, which is in concurrence with our previous in vitro data. Such a redistribution of vesicles impairs fast and effective neurotransmission, which likely contributes to learning and memory impairments found in models of Pb2+ intoxication. The mechanisms underlying this redistribution of vesicles likely involve reduced expression in presynaptic proteins, such synaptophysin and synaptobrevin as well as reduced phosphorylation of synapsin I. The mechanisms underlying changes in the Mossy Fiber – CA3 and Perforant Pathway – Dentate Gyrus terminals likely involve different pathways, which reflect the physiological heterogeneity of these various hippocampal regions. Uncovering behavioral and pharmacological interventions that could help to rescue the distribution of vesicles will likely promote fast and efficient neurotransmission.
Presynaptic active zone
Readily releasable pool
We would like to thank Mrs. Katerina Mancevska for her assistance in the care of animals that were used in this project and Dr. E. Charles Jenkins, Jr. for his proofreading of our manuscript. We would also like to thank the New York Institute for Basic Research for generous usage of their Electron Microscope and the City University of New York - College of Staten Island Advanced Imaging Facility.
This work was funded by NIEHS grants ES006189 and ES020465 to TRG.
Availability of supporting data and material
The datasets during and/or analyzed during the current study available from the corresponding author on reasonable request.
SRG performed perfusions, electron microscopy sample preparation, imaging and analysis, participated in experimental design drafted the manuscript. KHS and JMD bred and maintained experimental animals. TRG conceived the study, and participated in its design and drafted the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Animals were treated in accordance with the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85–23, revised 1996). The protocol was approved by Columbia University Institutional Animal Care and Use Committees (AC-AAAF4810).
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- Patel DR, Feucht C. Basic Concepts of Neurotransmission. Pediatr Clin N Am. 2011;581:21–31.View ArticleGoogle Scholar
- Südhof TC. Neurotransmitter release: the last millisecond in the life of a synaptic vesicle. Neuron. 2013;803:675–90.View ArticleGoogle Scholar
- Lasley SM, Gilbert ME. Presynaptic glutamatergic function in dentate gyrus in vivo is diminished by chronic exposure to inorganic lead. Brain Res. 1996;736:125–34.View ArticlePubMedGoogle Scholar
- Braga M, Edna FM, Pereira FR, Albuquerque E. Nanomolar concentrations of lead inhibit glutamatergic and GABAergic transmission in hippocampal neurons. Brain Res. 1999;826:22–34.View ArticlePubMedGoogle Scholar
- Neal AP, Guilarte TR. Molecular neurobiology of lead (Pb2+): effects on synaptic function. Mol Neurobiol. 2010;42:151–60.View ArticlePubMedPubMed CentralGoogle Scholar
- Nihei MK, Guilarte TR. Molecular changes in glutamatergic synapses induced by Pb2+: association with deficits of LTP and spatial learning. Neurotoxicology. 2001;22:635–43.View ArticlePubMedGoogle Scholar
- Sanders T, Liu Y, Buchner V, Tchounwou PB. Neurotoxic effects and biomarkers of lead exposure: a review. Rev Environ Health. 2009;24:15–46.View ArticlePubMedPubMed CentralGoogle Scholar
- Baranowska-Bosiacka I, Gutowska I, Nowacki M, Chlubek D. Neurotoxicity of lead. Hypothetical molecular mechanisms of synaptic function disorders. Neurol Neurochir Pol. 2012;46:69–578.Google Scholar
- Lasley SM, Green MC, Gilbert ME. Rat hippocampal NMDA receptor binding as a function of chronic lead exposure level. Neurotoxicol Teratol. 2001;23:185–9.View ArticlePubMedGoogle Scholar
- Markovac J, Goldstein GW. Picomolar concentrations of lead stimulate brain protein kinase C. Nature. 1988;334:71–3.View ArticlePubMedGoogle Scholar
- Xiao C, Gu Y, Zhou CY, Wang L, Zhang MM, Ruan D. Pb2+ impairs GABAergic synaptic transmission in rat hippocampal slices: a possible involvement of presynaptic calcium channels. Brain Res. 2006;1088:93–100.View ArticlePubMedGoogle Scholar
- Godwin HA. The biological chemistry of lead. Curr Opin Chem Biol. 2001;5:223–7.View ArticlePubMedGoogle Scholar
- Antonio-García MT, Massó-Gonzalez E. Toxic effects of perinatal lead exposure on the brain of rats: involvement of oxidative stress and the beneficial role of antioxidants. Food Chem Toxicol. 2008;46:2089–95.View ArticlePubMedGoogle Scholar
- Suszkiw JB. Presynaptic disruption of transmitter release by lead. Neurotoxicology. 2004;25:599–604.View ArticlePubMedGoogle Scholar
- Lidsky TI, Schneider JS. Lead neurotoxicity in children: basic mechanisms and clinical correlates. Brain. 2003;126:5–19.View ArticlePubMedGoogle Scholar
- Strużyńska L. A glutamatergic component of lead toxicity in adult brain: the role of astrocytic glutamate transporters. Neurochem Int. 2009;55:151–6.View ArticlePubMedGoogle Scholar
- Loikkanen J, Chvalova K, Naarala J, Vähäkangas KH, Savolainen KM. Pb2+-induced toxicity is associated with p53-independent apoptosis and enhanced by glutamate in GT1–7 neurons. Toxicol Letters. 2003;144:235–46.View ArticleGoogle Scholar
- Neal AP, Stansfield KH, Worley PF, Thompson RE, Guilarte TR. Lead exposure during synaptogenesis alters vesicular proteins and impairs vesicular release: potential role of NMDA receptor-dependent BDNF signaling. Toxicol Sci. 2010;116:249–63.View ArticlePubMedPubMed CentralGoogle Scholar
- Stansfield KH, Pilsner JR, Lu Q, Wright RO, Guilarte TR. Dysregulation of BDNF-TrkB signaling in developing hippocampal neurons by Pb2+: Implications for an environmental basis of neurodevelopmental disorders. Toxicol Sci. 2012;127:277–95.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang XL, Guariglia SR, McGlothan JL, Stansfield KH, Stanton PK, Guilarte TR. Presynaptic mechanisms of lead neurotoxicity: effects on vesicular release, vesicle clustering and mitochondria number. PLoS One. 2015;10:e0127461.View ArticlePubMedPubMed CentralGoogle Scholar
- Guilarte TR. Pb2+ inhibits NMDA receptor function at high and low affinity sites: developmental and regional brain expression. Neurotoxicology. 1996;18:43–51.Google Scholar
- Guilarte TR, Miceli RC, Jett DA. Neurochemical aspects of hippocampal and cortical Pb2+ neurotoxicity. Neurotoxicology. 1993;15:459–66.Google Scholar
- Almeida LEF, Murray PD, Zielke HR, Roby CD, Kingsbury TJ, Krueger BK. Autocrine activation of neuronal NMDA receptors by aspartate mediates dopamine-and cAMP-induced CREB-dependent gene transcription. J Neurosci. 2009;29:12702–10.View ArticlePubMedPubMed CentralGoogle Scholar
- Shupliakov O, Haucke V, Pechstein A. How synapsin I may cluster synaptic vesicles. Semin Cell Dev Biol. 2011;22:393–9.View ArticlePubMedGoogle Scholar
- Pechstein A, Shupliakov O. Taking a back seat: synaptic vesicle clustering in presynaptic terminals. Front Synaptic Neurosci. 2010;2:143.View ArticlePubMedPubMed CentralGoogle Scholar
- Bykhovskaia M. Synapsin regulation of vesicle organization and functional pools. Semin Cell Dev Biol. 2011;22:387–92.View ArticlePubMedGoogle Scholar
- Audesirk G, Audesirk T. Effects of inorganic lead on voltage-sensitive calcium channels in N1E-115 neuroblastoma cells. Neurotoxicology. 1991;12:519.PubMedGoogle Scholar
- Gutowski M, Altmann L, Sveinsson K, Wiegand H. Synaptic plasticity in the CA1 and CA3 hippocampal region of pre-and postnatally lead-exposed rats. Toxicol Lett. 1998;95:195–203.View ArticlePubMedGoogle Scholar
- Hollenbeck PJ, Saxton WM. The axonal transport of mitochondria. J Cell Sci. 2005;118:5411–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Palay S. Synapses in the central nervous system. J Biophys Biochem Cytol. 1956;2:193–202.View ArticlePubMedPubMed CentralGoogle Scholar
- He LA, Poblenz T, Medrano CJ, Fox DA. Lead and calcium produce rod photoreceptor cell apoptosis by opening the mitochondrial permeability transition pore. J Biol Chem. 2000;275:12175–84.View ArticlePubMedGoogle Scholar
- Fox DA, He LA, Poblenz AT, Medrano CJ, Blocker YS, Srivastava D. Lead-induced alterations in retinal cGMP phosphodiesterase trigger calcium overload, mitochondrial dysfunction and rod photoreceptor apoptosis. Toxicol Lett. 1998;102:359–61.View ArticlePubMedGoogle Scholar
- Gilbert ME, Mack CM, Lasley SM. Chronic developmental lead exposure increases the threshold for long-term potentiation in rat dentate gyrus in vivo. Brain Res. 1996;736:118–24.View ArticlePubMedGoogle Scholar
- Kuhlmann AC, McGlothan JL, Guilarte TR. Developmental lead exposure causes spatial learning deficits in adult rats. Neurosci Lett. 1997;233:101–4.View ArticlePubMedGoogle Scholar
- Abrahams S, Pickering A, Polkey CE, Morris RG. Spatial memory deficits in patients with unilateral damage to the right hippocampal formation. Neuropsychologia. 1997;35:11–24.View ArticlePubMedGoogle Scholar
- Cory-Slechta DA, Weston D, Liu S, Allen JL. Brain hemispheric differences in the neurochemical effects of lead, prenatal stress, and the combination and their amelioration by behavioral experience. Toxicol Sci. 2013;132:419–30.View ArticlePubMedPubMed CentralGoogle Scholar
- Nikonenko AG, Skibo GG. Technique to quantify local clustering of synaptic vesicles using single section data. Microsc Res Tech. 2004;65:287–91.View ArticlePubMedGoogle Scholar
- Rizzoli SO, Betz WJ. Synaptic vesicle pools. Nat Rev Neurosci. 2005;6:57–69.View ArticlePubMedGoogle Scholar
- Schikorski T, Stevens CF. Morphological correlates of functionally defined synaptic vesicle populations. Nat Neurosci. 2001;4:391–5.View ArticlePubMedGoogle Scholar
- Altman DG, Bland JM. Standard deviations and standard errors. Br Med J. 2005;331:903.View ArticleGoogle Scholar
- El-Husseini AED, Schnell E, Chetkovich DM, Nicoll RA, Bredt DS. PSD-95 involvement in maturation of excitatory synapses. Science. 2000;290:1364–8.PubMedGoogle Scholar
- Verina T, Rohde CA, Guilarte TR. Environmental lead exposure during early life alters granule cell neurogenesis and morphology in the hippocampus of young adult rats. Neuroscience. 2007;145:1037–47.View ArticlePubMedPubMed CentralGoogle Scholar