Distribution of P2X3 purinoceptor-immunoreactive sensory nerve endings in the carotid body of Japanese macaque (Macaca fuscata).

In the carotid body of laboratory rodents, adenosine 5'-triphosphate (ATP)-mediated transmission is regarded as critical for transmission from chemoreceptor type I cells to P2X3 purinoceptor-expressing sensory nerve endings. The present study investigated the distribution of P2X3-immunoreactive sensory nerve endings in the carotid body of the adult male Japanese monkey (Macaca fuscata) using multilabeling immunofluorescence. Immunoreactivity for P2X3 was detected in nerve endings associated with chemoreceptor type I cells immunoreactive for synaptophysin. Spherical or flattened terminal parts of P2X3-immunoreactive nerve endings were in close apposition to the perinuclear cytoplasm of synaptophysin-immunoreactive type I cells. Immunoreactivity for ectonucleoside triphosphate diphosphohydrolase 2 (NTPDase2), which hydrolyzes extracellular ATP, was localized in the cell body and cytoplasmic processes of S100B-immunoreactive cells. NTPDase2-immunoreactive cells surrounded P2X3-immunoreactive terminal parts and synaptophysin-immunoreactive type I cells, but did not intrude into attachment surfaces between terminal parts and type I cells. These results suggest ATP-mediated transmission between type I cells and sensory nerve endings in the carotid body of the Japanese monkey, as well as those of rodents.

[Posture Control Associated with Quadrupedal and Bipedal Gait in Japanese Monkeys (Macaca fuscata)].

How the CNS deals with instability of upright posture is the core in the control of bipedal gait. In this review, we summarize our recent findings comparing kinematics and EMG activity during quadrupedal and bipedal gait in Japanese macaques. Trunk/hindlimb muscles showed step cycle-modulated activity, which was more active in bipedal than in quadrupedal gait. For bipedal gait, enhanced activity during longer double support phase was predominantly observed in distal hindlimb muscles. Alternate burst activity in bilateral back muscles cyclically brought back the tilted trunk. In monkeys' quadrupedal gait, hindlimbs formed functional pairs with contralateral forelimbs, unlike in non-primate quadrupeds. These diagonal pairs acted differently on movements of the center of mass (COM). For bipedal gait, the hindlimbs solely carried the COM. Our results suggest that, compared to non-primate quadrupeds, hindlimbs in macaques contribute more critically to weight support and balance control even for quadrupedal gait. Additionally, for more unstable bipedal gait, the monkeys' CNS reinforces such hindlimb roles and actively controls the trunk posture in maintaining dynamic balance, in a manner similar to humans. Studies on Japanese macaques will further our understanding of the neural basis for the control of gait in mammals by bridging non-primate quadrupeds and humans.

Peroxidase-catalyzed microextrusion bioprinting of cell-laden hydrogel constructs in vaporized ppm-level hydrogen peroxide.

Hydrogels were prepared by contacting air containing 10-50 ppm H2O2 with an aqueous solution containing polymer(s) possessing phenolic hydroxyl (Ph) moieties (polymer-Ph) and horseradish peroxidase (HRP). In this system, HRP catalyzes cross-linking of the Ph moieties by consuming H2O2 diffused from the air. The hydrogelation rate and mechanical properties of the resultant hydrogels can be tuned by controlling the H2O2 concentration in air, the exposure time of the air containing H2O2 to the solution containing polymer-Phs and HRP, and the HRP concentration. The shortest hydrogelation time of the solution stirred in air containing 16 ppm H2O2 was 6 s. Based on these findings, this hydrogelation system was applied to microextrusion bioprinting, in which bioink containing polymer-Phs, HRP, and cells were extruded into air containing H2O2. The superior cytocompatibility of the bioprinting method was confirmed by more than 90% viability, migration, and the spreading of mouse fibroblast 10T1/2 cells enclosed in the bioprinted hydrogels composed of derivatives of hyaluronic acid and gelatin, both possessing Ph moieties. These results demonstrate the great potency of HRP-catalyzed hydrogelation consuming H2O2 supplied in surrounding air for various biomedical applications, especially bioprinting.

Anchoring PEG-oleate to cell membranes stimulates reactive oxygen species production.

Polyethylene glycol (PEG) derivatives possessing oleyl and reactive groups for conjugating functional substrates, such as proteins and quantum dots, are useful materials for cell-surface engineering and cell immobilization onto substrates. The reagent is known as a biocompatible anchor for cell membranes (BAM). Here, BAM-anchoring on cell membranes is reported to stimulate reactive oxygen species (ROS) production in those cells. Significant increases in ROS production and release to the surrounding environment were detected in mouse fibroblast cell line 10T1/2 when soaked in a solution containing BAM conjugated with 1/10mol/mol bovine serum albumin at 1.5µM-protein. ROS production stimulation was confirmed to be independent of the protein crosslinked with BAM and of cell type. Similar stimulation was detected for BAMs conjugated with ovalbumin and casein, in human hepatoma cell line HepG2, and human umbilical vein endothelial cells. Considering the effects of ROS on a variety of cellular processes, these results demonstrated the necessity for focusing attention on the effects of generated and released ROS on the behaviors of cells in the studies applying BAM to cells.

Prefrontal spatial working memory network predicts animal's decision making in a free choice saccade task.

While neurons in the lateral prefrontal cortex (PFC) encode spatial information during the performance of working memory tasks, they are also known to participate in subjective behavior such as spatial attention and action selection. In the present study, we analyzed the activity of primate PFC neurons during the performance of a free choice memory-guided saccade task in which the monkeys needed to choose a saccade direction by themselves. In trials when the receptive field location was subsequently chosen by the animal, PFC neurons with spatially selective visual response started to show greater activation before cue onset. This result suggests that the fluctuation of firing before cue presentation prematurely biased the representation of a certain spatial location and eventually encouraged the subsequent choice of that location. In addition, modulation of the activity by the animal's choice was observed only in neurons with high sustainability of activation and was also dependent on the spatial configuration of the visual cues. These findings were consistent with known characteristics of PFC neurons in information maintenance in spatial working memory function. These results suggest that precue fluctuation of spatial representation was shared and enhanced through the working memory network in the PFC and could finally influence the animal's free choice of saccade direction. The present study revealed that the PFC plays an important role in decision making in a free choice condition and that the dynamics of decision making are constrained by the network architecture embedded in this cortical area.

Opposing history effect of preceding decision and action in the free choice of saccade direction.

When we act voluntarily, we make a decision to do so prior to the actual execution. However, because of the strong tie between decision and action, it has been difficult to dissociate these two processes in an animal's free behavior. In the present study, we tried to characterize the differences in these processes on the basis of their unique history effect. Using simple eye movement tasks in which the direction of a saccade was either instructed by a computer or freely chosen by the subject, we found that the preceding decision and action had different effects on the animal's subsequent behavior. While choosing a direction (previous decision) produced a positive history effect that prompted the choice of the same saccade direction, making a saccadic response to a direction (previous action) produced a negative history effect that discouraged the monkey from choosing the same direction. This result suggests that the history effect in sequential behavior reported in previous studies was a mixture of these two different components. Future studies on decision-making need to consider the importance of the distinction between decision and action in animal behavior.