Custom-engineered hydrogels for delivery of human iPSC-derived neurons into the injured cervical spinal cord.

Cervical damage is the most prevalent type of spinal cord injury clinically, although few preclinical research studies focus on this anatomical region of injury. Here we present a combinatorial therapy composed of a custom-engineered, injectable hydrogel and human induced pluripotent stem cell (iPSC)-derived deep cortical neurons. The biomimetic hydrogel has a modular design that includes a protein-engineered component to allow customization of the cell-adhesive peptide sequence and a synthetic polymer component to allow customization of the gel mechanical properties. In vitro studies with encapsulated iPSC-neurons were used to select a bespoke hydrogel formulation that maintains cell viability and promotes neurite extension. Following injection into the injured cervical spinal cord in a rat contusion model, the hydrogel biodegraded over six weeks without causing any adverse reaction. Compared to cell delivery using saline, the hydrogel significantly improved the reproducibility of cell transplantation and integration into the host tissue. Across three metrics of animal behavior, this combinatorial therapy significantly improved sensorimotor function by six weeks post transplantation. Taken together, these findings demonstrate that design of a combinatorial therapy that includes a gel customized for a specific fate-restricted cell type can induce regeneration in the injured cervical spinal cord.

Imaging cells in the developing nervous system with retrovirus expressing modified green fluorescent protein.

To visualize the movements of cells and their processes in developing vertebrates, we constructed replication-incompetent retroviral vectors encoding green fluorescent protein (GFP) that can be detected as a single integrated copy per cell. To optimize GFP expression, the CMV enhancer and avian beta-actin promoter were incorporated within a retrovirus construct to drive transcription of redshifted (F64L, S65T) and codon-modified GFP (EGFP), EGFP tagged with GAP-43 sequences targeting the GFP to the cell membrane, or EGFP with additional mutations that increase its ability to fold properly at 37 degrees C (S147P or V163A, S175G). We have used these viruses to efficiently mark and follow the developmental progression of a large population of cells in rat neocortex and whole avian embryos. In the chick embryo, the migration and development of GFP-marked neural crest cells were monitored using time-lapse videomicroscopy. In the neocortex, GFP clearly delineates the morphology of a variety of neuronal and glial phenotypes. Cells expressing GFP display normal dendritic morphologies, and infected cells persist into adulthood. Cortical neurons appear to form normal local axonal and long-distance projections, suggesting that the presence of cytoplasmic or GAP-43-tagged GFP does not significantly interfere with normal development.

Modulation of oscillator interactions in the crab stomatogastric ganglion by crustacean cardioactive peptide.

The modulation of the pyloric rhythm of the stomatogastric ganglion of the crab, Cancer borealis, by crustacean cardioactive peptide (CCAP) is described. CCAP activated pyloric rhythms in most silent preparations, and altered the phase relationships of pyloric motor neuron firing in all preparations. In CCAP, the pyloric rhythms were characterized by long lateral pyloric (LP) neuron bursts of action potentials. The threshold for CCAP action was approximately 10(-10) M, with increasing effects at higher CCAP concentrations. The changes in motor pattern evoked by CCAP produced significant changes in LP-innervated muscle movement. These movements were additionally potentiated by CCAP applications to isolated nerve-muscle preparations. Thus, enhanced motor neuron firing and increase of the gain of the neuromuscular junctions are likely to operate coordinately in response to hormonally released CCAP. High CCAP concentrations sometimes resulted in modification of the normal 1:1 alternation between the pyloric dilator (PD) and LP neurons to patterns of 2:1, 3:1, or 4:1 alternation. CCAP seems to activate slow intrinsic oscillations in the LP neuron, as well as enhance faster oscillations in the pacemaker group of PD/anterior burster (AB) neurons. Simulations of fast and slow oscillators with reciprocal inhibitory coupling suggest mechanisms that could account for the mode switch from 1:1 alternation to multiple PD bursts alternating with one LP neuron burst.

Switching neurons are integral members of multiple oscillatory networks.

BACKGROUND: The stomatogastric ganglion of the crab Cancer borealis contains the neurons that generate several different behaviors, such as the fast pyloric rhythm and the slower gastric-mill rhythm. It has previously been shown that many stomatogastric ganglion neurons can switch between pyloric- and gastric-timed activity. However, the question remained whether these neurons really are integral members of several central-pattern-generating networks, or just passive followers that only change their activity patterns in response to a switch determined by other neurons. RESULTS: To address this question, we perturbed the activity of the 'pyloric' ventricular dilator neuron and the 'gastric' lateral gastric neuron during ongoing pyloric and gastric rhythms. In the absence of ongoing gastric rhythms, these neurons can fire in pyloric time, and perturbing them can reset the pyloric rhythm. During robust gastric activity, the lateral gastric and ventricular dilator neurons can fire in gastric time, and perturbing them can reset the gastric rhythm. CONCLUSIONS: When stomatogastric ganglion neurons change their firing patterns, they also function as part of the circuitry that generates the new rhythm with which they are firing, demonstrating that individual neurons can be used as part of multiple pattern-generating circuits.

Differential expression of synaptic vesicle protein 2 (SV2) isoforms.

The synaptic vesicle proteins SV2A and SV2B (SV2 = synaptic vesicle protein 2) are two highly related proteins belonging to a family of transporters. As a first step toward identifying the function of the SV2 proteins, we examined the expression of SV2A and SV2B in the rat brain by in situ hybridization, immunohistochemistry, and immunoprecipitation with isoform-specific antibodies. These analyses revealed that one isoform, SV2A, is expressed ubiquitously throughout the brain at varying levels. The other isoform, SV2B, has a more limited distribution with varying degrees of coexpression with SV2A. Immunoprecipitation of brain synaptic vesicles with isoform-specific antibodies followed by Western analyses suggests that both isoforms can be present on the same synaptic vesicle. The expression of the SV2 proteins did not correlate either with neurotransmitter phenotype or with the expression of other synaptic vesicle protein isoforms. SV2B expression was observed to change during development; it is more widely expressed in the immature brain and is found in cells that have yet to establish synaptic contacts. The ubiquitous and overlapping expression of the SV2s suggests that they perform a function common to all synaptic vesicles. Variable and changing coexpression of the SV2 isoforms may indicate that SV2 function is regulated by the isoform composition of synaptic vesicles. The observation that the synaptic vesicle proteins, all occurring in multiple isoforms, are differentially expressed with respect to each other indicates that up to 90 different vesicle types are possible.

The effects of SDRNFLRFamide and TNRNFLRFamide on the motor patterns of the stomatogastric ganglion of the crab Cancer borealis.

TNRNFLRFamide was isolated and sequenced from the stomatogastric nervous system of the crab Cancer borealis by reverse-phase high performance liquid chromatography followed by automated Edman degradation. An SDRNFLRFamide-like peptide that exactly co-migrated with SDRNFLRFamide was also observed. The effects of TNRNFLRFamide and SDRNFLRFamide on the gastric and pyloric rhythms of the stomatogastric nervous system of the crab Cancer borealis were studied. Both peptides activated pyloric rhythms in quiescent preparations in a dose-dependent manner with a threshold between 10(-11) and 10(-10) mol l-1. Both peptides increased the pyloric rhythm frequency of preparations showing moderate activity levels and had relatively little effect on preparations that showed strong pyloric rhythms prior to peptide application. Both peptides evoked gastric mill activity in preparations without existing gastric rhythms. The activation of the gastric rhythm is associated with activation of oscillatory properties in the dorsal gastric neurone. The induction of gastric rhythms by these peptides was accompanied by switches from pyloric-timed activity to gastric-timed activity by several stomatogastric ganglion neurones. Application of these peptides provides direct experimental control of circuit modification in the stomatogastric nervous system.

The behavioral repertoire of the gastric mill in the crab, Cancer pagurus: an in situ endoscopic and electrophysiological examination.

Simultaneous endoscopic and electrophysiological recordings were used to observe the behavior of the gastric mill complex while recording the motor output of the stomatogastric ganglion (STG) in intact crabs. In the crab STG, many pattern-generating neurons are able to fire in several distinct rhythmic motor patterns. Specifically, many neurons can switch between firing in time with the rapid pyloric rhythm to firing in time with the slower gastric mill rhythm (Weimann et al., 1991). We now correlate behaviorally relevant movements of the gastric mill with some of the modifications of neuronal firing patterns previously characterized using in vitro STG preparations. The intracellular and extracellular recordings from the intact crab are largely indistinguishable from those obtained from in vitro preparations. For the first time, we describe the movements that result as neurons switch their activity patterns associated with activation of the gastric mill rhythm. Extracellular stimulation and intracellular depolarization of individual motor neurons is used to determine the relationship between frequency of firing and movement in behaving animals.

Multiple axonal spike initiation zones in a motor neuron: serotonin activation.

The lateral gastric (LG) motor neuron of the stomatogastric nervous system of the crab Cancer borealis has a large soma in the stomatogastric ganglion (STG). The LG motor neuron makes inhibitory synaptic connections within the neuropil of the STG, and also projects to the periphery, where it innervates a series of muscles that control the movements of the lateral teeth of the gastric mill. The LG motor neuron has a spike initiation zone close to its neuropilar integrative regions, from which spikes propagate orthodromically to the muscles. Additionally, under certain conditions, the LG neuron can initiate spikes at peripheral axonal sites that can be 0.5-2.0 cm from the STG. Peripherally initiated spikes propagate antidromically into the STG and also propagate to the muscle. The peripheral spike initiation zones are often active in combined preparations in which the muscles are left attached. When the muscles are removed, depolarization of the LG soma together with 5-HT applied to the motor nerve also evokes peripheral spike initiation. At a given 5-HT concentration, the duration of the trains of antidromic spikes can be controlled by current injection into the soma, suggesting the presence of a slow voltage-dependent conductance in the LG axon. The antidromic spikes contribute to lengthening of the duration of contraction in some of the muscles innervated by the LG, but do not evoke IPSPs onto LG follower neurons. Thus, the LG neuron can send different signals to its peripheral and central targets.

Neurons that form multiple pattern generators: identification and multiple activity patterns of gastric/pyloric neurons in the crab stomatogastric system.

1. The stomatogastric ganglion (STG) of decapod crustaceans has been characterized by its production of two motor patterns, the gastric mill rhythm and the pyloric rhythm. The period of the gastric rhythm is typically 5-10 s, whereas the period of the pyloric rhythm is approximately 1 s. 2. In the STG of the crab, Cancer borealis, we find routinely that many motor neurons are active in time with both the pyloric and gastric rhythms. We rigorously identified the motor neurons according to the muscles they innervate. Some neurons usually classified as members of the pyloric network can be active in time with the gastric rhythm. All of the gastric motor neurons except the dorsal gastric (DG) neuron can generate pyloric-timed firing patterns. 3. Two motor neurons innervate muscles found in several different regions of the stomach. The inferior cardiac (IC) neuron, usually considered part of the pyloric network, innervates cardiac sac, gastric mill, and pyloric muscles. The lateral posterior gastric (LPG) neurons innervate muscles of both the gastric mill and the pyloric chamber. 4. These data show that the gastric and pyloric networks in the crab are not separate groups of neurons that independently generate two different rhythmic behaviors. Rather, these neurons together provide a synaptically connected pool of neurons from which many different pattern-generating circuits can be assembled, under different physiological conditions.