P. Johannes Helm

Water entry into astrocytes during brain edema formation

The process of brain edema formation has been studied extensively at the macroscopic level. In contrast, little is known about water fluxes and volume changes at the cellular level in the initial phase of brain edema. Insight in these “microscopic” events could pave the way for more efficient prevention and therapy. Here, we report measurements of brain cell volume responses recorded in vivo in a model of systemic hyponatremia. Transgenic mice expressing fluorescent proteins in astrocytes were subjected to hypo‐osmotic stress and two photon laser scanning microscopy. Volume measurements of glial cells in the cerebellum and the visual cortex indicate that individual astrocytes undergo a position‐dependent increase in cell volume by a factor of two or more during edema formation. Our data are the first to show that volume changes can be monitored at the cellular level in vivo and demonstrate that astrocytes are sites of water entry in the initial phase of brain edema formation. The uptake of water in astrocytes is likely to reflect the strong expression of aquaporin‐4 in these cells.

Dynamics of Ionic Shifts in Cortical Spreading Depression

Cortical spreading depression is a slowly propagating wave of near-complete depolarization of brain cells followed by temporary suppression of neuronal activity. Accumulating evidence indicates that cortical spreading depression underlies the migraine aura and that similar waves promote tissue damage in stroke, trauma, and hemorrhage. Cortical spreading depression is characterized by neuronal swelling, profound elevation of extracellular potassium and glutamate, multiphasic blood flow changes, and drop in tissue oxygen tension. The slow speed of the cortical spreading depression wave implies that it is mediated by diffusion of a chemical substance, yet the identity of this substance and the pathway it follows are unknown. Intercellular spread between gap junction-coupled neurons or glial cells and interstitial diffusion of K+ or glutamate have been proposed. Here we use extracellular direct current potential recordings, K+-sensitive microelectrodes, and 2-photon imaging with ultrasensitive Ca2+ and glutamate fluorescent probes to elucidate the spatiotemporal dynamics of ionic shifts associated with the propagation of cortical spreading depression in the visual cortex of adult living mice. Our data argue against intercellular spread of Ca2+ carrying the cortical spreading depression wavefront and are in favor of interstitial K+ diffusion, rather than glutamate diffusion, as the leading event in cortical spreading depression.

Neurobiology: How hardwired is the brain?

In a technological breakthrough, two groups have shown that it is possible to study the turnover of spines — tiny protrusions on nerve cells — in live mice. But its still uncertain just how dynamic the spines are.

Stimulation-Evoked Ca2+ Signals in Astrocytic Processes at Hippocampal CA3–CA1 Synapses of Adult Mice Are Modulated by Glutamate and ATP

To date, it has been difficult to reveal physiological Ca2+ events occurring within the fine astrocytic processes of mature animals. The objective of the study was to explore whether neuronal activity evokes astrocytic Ca2+ signals at glutamatergic synapses of adult mice. We stimulated the Schaffer collateral/commissural fibers in acute hippocampal slices from adult mice transduced with the genetically encoded Ca2+ indicator GCaMP5E driven by the glial fibrillary acidic protein promoter. Two-photon imaging revealed global stimulation-evoked astrocytic Ca2+ signals with distinct latencies, rise rates, and amplitudes in fine processes and somata. Specifically, the Ca2+ signals in the processes were faster and of higher amplitude than those in the somata. A combination of P2 purinergic and group I/II metabotropic glutamate receptor (mGluR) antagonists reduced the amplitude of the Ca2+ transients by 30–40% in both astrocytic compartments. Blockage of the mGluRs alone only modestly reduced the magnitude of the stimulation-evoked Ca2+ signals in processes and failed to affect the somatic Ca2+ response. Local application of group I or I/II mGluR agonists or adenosine triphosphate (ATP) elicited global astrocytic Ca2+ signals that mimicked the stimulation-evoked astrocytic Ca2+ responses. We conclude that stimulation-evoked Ca2+ signals in astrocytic processes at CA3–CA1 synapses of adult mice (1) differ from those in astrocytic somata and (2) are modulated by glutamate and ATP.

The use of femto-second lasers to trigger powerful explosions of gold nanorods to destroy cancer cells.

Gold nanorods (AuNRs) with an aspect ratio of 3-4 exhibit large cross sections for single and multi photon light absorption processes in the near infrared region due to surface plasmon resonances. 800 nm laser pulses with the 150 fsec pulse duration (fs laser) can trigger explosions of AuNRs. The fs laser pulses at 20 W/mm(2) equivalent continuous wave (cw) power density blasted AuNRs in QGY human carcinoma cells as confirmed using transmission electron microscopy, while a cw laser at the same power density and dose did not. Cell survival studies further demonstrated that the cw laser at a dose of 15 J/mm(2) resulted in the death of 15% of AuNRs-loaded cells, probably due to a photothermal effect, while the fs laser at only 1.5 J/mm(2) killed more than 90% of AuNRs-loaded cells, indicating that the fs laser-triggered explosions of intracellular AuNRs are powerful enough to instantaneously kill tumour cells.

Analysis of optical properties of the mouse cranium--implications for in vivo multi photon laser scanning microscopy.

Trans-cranial imaging is the least invasive method for optical in vivo studies of structures in the mouse brain and has found wide application over the last few years. An important issue is how and to what extent the cranium and the tissue between the cranium and the focal point detract from the quality of the recorded images. Here we address this issue by recording transmission images in wild type mice at five wavelengths in the visible and near-infrared spectrum. The recorded laser scanning microscopic images were analyzed pixel by pixel in order to quantify the light attenuation and shading as function of the location of the focal point relative to the cranium. Additional images demonstrate the effects of the mouse crania on the images of fluorescent microspheres in the low micrometer range. The results of this study demonstrate that light attenuation by the cranium, though with typical losses of less than 20% of the incident light, induces shading effects during the imaging process. Geometrical shapes and sizes in the images of the recorded objects may differ substantially depending on whether they have been recorded trans-cranially or not. This is true even for comparatively large structures such as cell somata. Our results call for a more realistic appraisal of the potential of the trans-cranial imaging approach, particularly when it comes to absolute measurements of sizes and shapes of small objects. As trans-cranial imaging has found wide use in contemporary research it is important that the results be interpreted with due caution.

A multiphoton laser scanning microscope setup for transcranial in vivo brain imaging on mice

We describe a multiphoton laser scanning microscope setup for transcranial in vivo brain imaging in mice. The modular system is based on a modified industrial standard Confocal Scanning Laser Microscope (CSLM) and is assembled mainly from commercially available components. A special multifunctional stage, which is optimized for both laser scanning microscopic observation and preparative animal surgery, has been developed and built. The detection unit includes a highly efficient photomultiplier tube installed in a Peltier-cooled thermal box shielding the detector from changes in room temperature and from distortions caused by external electromagnetic fields. The images are recorded using a 12-bit analog–to–digital converter. Depending on the characteristics of the staining, individual nerve cells can be imaged down to at least 100μm below the intact cranium and down to at least 200μm below the opened cranium.

Deletion of Aquaporin-4 curtails extracellular glutamate elevation in cortical spreading depression in awake mice

Abstract Cortical spreading depression (CSD) is a phenomenon that challenges the homeostatic mechanisms on which normal brain function so critically depends. Analyzing the sequence of events in CSD holds the potential of providing new insight in the physiological processes underlying normal brain function as well as the pathophysiology of neurological conditions characterized by ionic dyshomeostasis. Here, we have studied the sequential progression of CSD in awake wild‐type mice and in mice lacking aquaporin‐4 (AQP4) or inositol 1,4,5‐triphosphate type 2 receptor (IP3R2). By the use of a novel combination of genetically encoded sensors that a novel combination ‐ an unprecedented temporal and spatial resolution, we show that CSD leads to brisk Ca2+ signals in astrocytes and that the duration of these Ca2+ signals is shortened in the absence of AQP4 but not in the absence of IP3R2. The decrease of the astrocytic, AQP4‐dependent Ca2+ signals, coincides in time and space with a decrease in the duration of extracellular glutamate overflow but not with the initial peak of the glutamate release suggesting that in CSD, extracellular glutamate accumulation is extended through AQP4‐dependent glutamate release from astrocytes. The present data point to a salient glial contribution to CSD and identify AQP4 as a new target for therapy.

Local impact of perivascular plaques on cerebral blood flow dynamics in a transgenic mouse model of Alzheimer's disease

Cerebrovascular pathology is closely coupled to cognitive function decline, as indicated by numerous studies at the system level. To better understand the mechanisms of this cognitive decline it is important to resolve how pathological changes in the vasculature - such as perivascular plaques - affect local cerebral blood flow dynamics. This issue is ideally studied in the intact brain at very high spatial resolution. Here, we describe initial results obtained by an approach based on in vivo observation by multi-photon microscopy of vascular plaques and local blood flow measurements in a transgenic mouse model engineered to express the human amyloid precursor protein with the Swedish and Arctic mutations. These mice exhibit a striking abundance of perivascular plaques in the cerebral cortex and are well suited to investigate vascular pathology in Alzheimers disease.

Optical effects of the cranium in trans-cranial in vivo two photon laser scanning microscopy in mice

The combination of multi photon laser scanning microscopy with transgenic techniques has set the stage for in vivo studies of long term dynamics of the central nervous system in mice. Brain structures located within 100?m to 200?m below the brain surface can be observed minimum-invasively during the post-adolescent life of the animal. However, even when selecting the most appropriate microscope optics available for the purpose, trans-cranial observation is compromised by the aberrations induced by the cranium and the tissue interposed between the cranium and the actual focus. It still is an un-resolved task to calculate these aberrational effects or to, at least, estimate quantitatively the distortions they induce onto the recorded images. Here, we report about measurements of the reflection, the absorption, and the effects on the objective point spread function of the mouse cranium as a function of the thickness of the cranium, the locus of trans-cranial observation and the wavelength. There is experimental evidence for pronounced Second Harmonic Generation (SHG) effects.