Synaptology of the inner plexiform layer in the anuran retina

The inner plexiform layer of the retina is a synaptic layer mostly devoid of perikarya. It contains the processes of three major neuron types: the bipolar cells, which carry information from the photoreceptors, the ganglion cells, which are the output elements of the retina, and the amacrine cells, which are able to influence the communication between the former two. Since amacrine cells are the most diverse retinal neurons, they are in a position to carve out and delineate the neural circuits of the inner retina. The aim of this review is to offer a summary of findings related to the general synaptology of the inner retina in frogs and also to provide some insight into the synaptic organization of neurochemically identified amacrine cells. The main conclusions of this paper are as follows: (i) Most contacts are formed between amacrine cells. (2) Direct bipolar to ganglion cell synapses exist, but are rare in the anuran retina. (3) All neurochemically identified amacrine cell types receive inputs from bipolar cells, but not all of them form reciprocal contacts with bipolar cell axon terminals. (4) A major inhibitory transmitter, gamma-aminobutyric acid, is involved in more than 50% of the synapses. Since contacts between inhibitory elements were often observed, disinhibitory circuits must also play a role in retinal information processing. (5) Reciprocal relationship between dopaminergic and gamma-aminobutyric acid-containing cells have been confirmed. Similar situation was observed in case of serotoninergic and gamma-aminobutyric acid-positive elements. No contacts were verified between serotoninergic and dopaminergic elements. (6) Both monoamine- and neuropeptide-containing amacrine cells establish direct contacts with ganglion cell dendrites, providing a morphological basis for neuromodulatory influence on the output elements of the retina. Unfortunately, only a handful of studies have been carried out to identify the synaptic connections between neurochemically identified cells in the anuran retina. Double-label studies at the electron microscope level to reveal the synaptic relationship of cell populations containing two different transmitters/modulators are extremely rare. Further insight into retinal synaptic circuitries could be gained with a combination of electrophysiology and morphology at the electron microscopic level. These studies must also involve identification of the transmitter receptors on identified cell types. Only after this step can the function of different synaptic circuitries be better approximated.     

Synaptic morphology of inner and outer hair cells of the human organ of Corti

Innervations of inner and outer hair cells of the organ of Corti of the human cochlea were studied by serial section electron microscopy. At the base of inner hair cells, presumed afferent fibers were of varying size and demonstrated synaptic specialization consisting of a presynaptic body, vesicles, and asymmetrical synaptic membrane specialization. Two types of neurons, vesiculated presumably efferent and nonvesiculated presumably afferent, synapsed at the base of outer hair cells. The synaptic specialization of afferent fibers included presynaptic body, vesicles, and asymmetrical membrane thickening, whereas efferent synapses demonstrated presynaptic vesicles and a subsynaptic cisterna. Some presumably afferent nerve terminals formed a reciprocal synapse with outer hair cells in both the human and the chimpanzee. Such a synaptic relationship demonstrated morphologic specialization consistent with both hair cell-to-neuron and neuron-to-hair cell transmission between the same outer hair cell and nerve terminal. The innervation density of inner and outer hair cells and the comparative anatomy of the afferent and efferent innervation are discussed.     

Biochemical and morphological differentiation of acetylcholinesterase-positive efferent fibers in the mouse cochlea

We have compared the biochemical expression of cholinergic enzymes with the morphological differentiation of efferent nerve fibers and endings in the cochlea of the postnatally developing mouse. Choline acetyltransferase (ChAT) and acetylcholinesterase (AChE) are present in the newborn cochlea at specific activities 63% and 25%, respectively, of their mature levels. The relative increases in ChAT, in AChE, and in its molecular forms over the newborn values start about day 4 and reach maturity by about day 10. The biochemical results correlate well with the massive presence of nerve fibers stained immunocytochemically for ChAT and AChE or enzymatically for AChE in the inner and outer hair cell regions. Ultrastructural studies, however, indicate the presence of only few vesiculated fibers and endings in the inner and outer hair cell regions. The appearance of large, cytologically mature endings occurs only toward the end of the third postnatal week. The discrepancy may be resolved in the electron microscope using the enzymatic staining for AChE. Labeling is seen on many nonvesiculated fibers and endings in the hair cell regions, suggesting that the majority of the efferent fibers in the perinatal organ may be biochemically differentiated but morphologically immature. The results may imply that the efferents to inner and outer hair cells develop earlier than indicated by previous ultrastructural studies. Moreover, the pattern of development suggests that in the cochlea, as in other tissues, the biochemical differentiation of the efferent innervation may precede the morphological maturation.     

Neuromodulation of ligand- and voltage-gated channels in the amphibian retina

To understand information processing in the retina, it is important to identify and characterize the types of synaptic receptors and intrinsic ion channels in retinal neurons. In order to achieve a high degree of adaptability, retinal synapses have evolved multiple neuromodulatory mechanisms. Light or modulatory agents can alter the efficacies of both electrical and chemical synaptic transmission in the retina. Recent studies indicate that interaction of voltage-gated channels with those activated by neurotransmitters plays a significant role in shaping the light-evoked postsynaptic responses of retinal neurons. The fact that both types of channels are subject to modulation by multiple second messenger-mediated intracellular processes is a clear indicator of the importance of neuromodulation in retinal function. The whole-cell patch clamp technique provides a means to study mechanisms of regulation of ion channels by controlling intracellular as well as the extracellular environment. This review describes the experimental evidence, mostly obtained in our laboratory, which indicates the important role of Ca-dependent neuromodulatory processes in the regulation of signal transmission in the vertical pathway of the amphibian retina.     

Scanning electron microscopy of nerve fibers in human fetal cochlea

The cochleas of four human fetuses ranging 22–25 weeks gestation were studied by scanning electron microscopy (SEM) for the purpose of obtaining a better understanding of the nerve fiber arrangement in the human ear. After critical point drying, the specimens were dissected and the floor of the tunnel of Corti and the outer wall of Nuel's space were exposed for observation. Upper cochlear turns, especially the apical turn, seemed to be still immature. Observed nerve fibers were classified into three types:

• 1 Spiral fibers: Fibers traveling basalward and following the shape of the cochlea were found in both the tunnel of Corti and Nuel's space and believed to be the afferent nerves responsible for innervating the outer hair cells
• 2 Radial fibers: radiating outward from the osseous spiral lamina—one such radial fiber transversing high in the tunnel space (supposedly the efferent nerve servicing the outer hair cells), and another sort of radial fiber (found crossing the tunnel floor), the nature of which was uncertain.
• 3 Irregular fibers: Consisting of thin, randomly running fibers within the cochlea. The destination of these fibers was not determined, but possibly they represent transitory nerve branchings of afferent or more probably efferent nerves, which would later regress during maturation.

     

Immunoelectron microscopic localization of neurotransmitters in the cochlea

This paper presents the works and methods of our respective laboratories using electron microscopic immunocytochemistry to identify and localize cochlear neurotransmitters. Antibodies to various prospective neurotransmitters and associated enzymes have been used to study the ultrastructural localization of several candidates for olivocochlear efferent neurotransmitters previously suggested by light microscopic immunocytochemistry. Antibodies against enkephalins label lateral olivocochlear efferent fibers. Antibodies against choline acetyltransferase (ChAT) (an enzyme marker for acetylcholine) label a major population of both lateral and medial efferent fibers and terminals, whereas antibodies to γ-aminobutyric acid (GABA) label what might be a small subpopulation of both the lateral and medial efferent systems. The GABA-like immunostained medial efferent fibers are preferentially located in the upper turns of the guinea pig cochlea, particularly the third turn. Immunoelectron microscopy shows that neither GABA nor ChAT immunolabels all medial efferent terminals, regardless of cochlear turn. All the different types of immunolabeled efferent terminals have been observed to make characteristic synaptic contacts; lateral efferent terminals on afferent dendrites and medial efferent terminals on outer hair cells and occasionally on type II afferent dendrites. Other types of contacts involving GABA-like, and sometimes met-enkephalin-like, immunostained fibers are occasionally seen particularly in the upper turns of the cochlea. Immunoelectron microscopic results suggest that both medial and lateral efferent systems might be further subdivided on the basis of differences in neurotransmitters. Future trends of immunocytochemical research on cochlear neurotransmitters are proposed, particularly colocalization studies, which show a complex pattern of coexistence of neurotransmitters in the lateral efferent system.     

Expression of TRPV4 in the zebrafish retina during development

The transient receptor potential (TRP) channels are involved in sensing mechanical/physical stimuli such as temperature, light, pressure, as well as chemical stimuli. Some TRP channels are present in the vertebrate retina, and the occurrence of the multifunctional channel TRP vanilloid 4 (TRPV4) has been reported in adult zebrafish. Here, we investigate the expression and distribution of TRPV4 in the retina of zebrafish during development using polymerase chain reaction (PCR), Western blot, and immunohistochemistry from 3 days post fertilization (dpf) until 100 dpf. TRPV4 was detected at the mRNA and protein levels in the eye of zebrafish at all ages sampled. Immunohistochemistry revealed the presence of TRPV4 in a population of the retinal cells identified as amacrine cells on the basis of their morphology and localization within the retina, as well as the co-localization of TRPV4 with calretinin. TRPV4 was first (3 dpf) found in the soma of cells localized in the inner nuclear and ganglion cell layers, and thereafter (10 dpf) also in the inner plexiform layer. The adult pattern of TRPV4 expression was achieved by 40 dpf the expression being restricted to the soma of some cells in the inner nuclear layer and ganglion cell layers. These data demonstrate the occurrence and developmental changes in the expression and localization of TRPV4 in the retina of zebrafish, and suggest a role of TRPV4 in the visual processing.     

Ultrastructure of motor nerve terminals in the anterior third of wistar rat tongue

The nerve terminals of intrinsic muscular fibers of the tongue of adult wistar rats was studied by using silver impregnation techniques, transmission electron microscopy (TEM), and high resolution scanning electron microscopy (HRSEM) to observe the nerve fibers and their terminals. Silver impregnation was done according to Winkelman and Schmit, 1957 . For TEM, small blocks were fixed in modified Karnovsky solution, postfixed in 1% buffered osmium tetroxide solution, and embedded in Spurr resin. For HRSEM, the parts were fixed in 2% osmium tetroxide solution with 1/15 M sodium phosphate buffer (pH 7.4) at 4°C for 2 h, according to the technique described by Tanaka, 1989 . Thick myelinated nerve bundles were histologically observed among the muscular fibers. The intrafusal nerve fiber presented a tortuous pathway with punctiform terminal axons in clusters contacting the surface of sarcolemma. Several myelinated nerve fibers involved by collagen fibers of the endoneurium were observed in HRSEM in three-dimensional aspects. The concentric lamellae of the myelin sheath and the axoplasm containing neurofilaments interspersed among the mitochondria were also noted. In TEM, myofibrils, mitochondria, rough endoplasmic reticulum, Golgi's apparatus, and glycogen granules were observed in sarcoplasm. It is also noted that the sarcomeres constituted by myofilaments with their A, I, and H bands and the electron dense Z lines. In areas adjacent to muscular fibers, there were myelinated and unmyelinated nerve fibers involved by endoneurium and perineurium. In the region of the neuromuscular junction, the contact with the sarcolemma of the muscular cell occurs forming several terminal buttons and showing numerous evaginations of the cell membrane. In the terminal button, mitochondria and numerous synaptic vesicles were observed. Microsc. Res. Tech., 2009. © 2009 Wiley-Liss, Inc.     

基于CPU＋GPU异构系统的棉花异纤识别系统

棉花中的异性纤维给棉纺织企业带来了不小的损失,因此开发出高效率的异纤分拣机是很多纺织企业的迫切需求。现有的异纤分拣机虽然能够达到剔除部分异纤的效果,但由于图像处理运算都是在工控机上的CPU里实现,为了达到在线实时检测的需求,只能采用比较简单的识别算法,异纤识别效果不是很理想。本文通过研究基于CPU＋GPU异构系统的棉花异纤识别系统,让GPU通过并行运算来实现异纤的识别算法,从而大大提高了运算效率,有效的减少了算法的运行时间,为复杂的异纤识别算法在异纤识别系统的使用提供了条件,从而有效提高异纤杂质的剔除率。实验表明,基于CPU＋GPU异构系统对算法的时间提高了十几倍。     

Efferent innervation of photoreceptors in spiders

The anterior median (AM) eye of the nocturnal spider Araneus ventricosus showed a marked circadian oscillation of sensitivity, but that of the diurnal spider Menemerus confusus showed no circadian oscillation. The AM eyes of the noct/diurnal spiders Argiope amoena and A. bruennichii have two types of photoreceptor cells with different sensitivities. The more sensitive cells showed a circadian oscillation of sensitivity, but the less sensitive cells did not. The circadian sensitivity change of the eyes was controlled by efferent neurosecretory fibers in the optic nerve. Illuminating the brain increased the frequency of efferent impulses in the optic nerve of Argiope, showing that certain photosensitive neurons are present in the brain. However, it seemed that the cerebral photosensitive neurons may be different from the efferent neurosecretory cells. The response of the cerebral photosensitive neurons increased transiently following diminution of the light intensity striking the eyes. The interaction between the cerebral photosensitive neurons and the eyes seemed to play a role in increasing this response.     

棉花异性纤维的动态识别技术研究

针对棉花异性纤维含量检验过程中手工挑拣方法存在的效率低、误差大等实际问题,研制了一种棉花异性纤维分析仪.该仪器利用皮棉开松机对皮棉进行充分开松,形成不间断均匀棉层,利用线扫描相机对流动棉层进行图像采集.首先对棉花异性纤维原始图像进行灰度处理;再采用自适应阈值技术和滤波技术完成棉花异性纤维图像分割和增强处理,得出清晰的二值化图像;然后采用挖空内点法和邻域搜索法进行轮廓提取,得出异性纤维的特征参数;最后以粗糙集理论为基础,完成了异性纤维的分类识别与重量统计.实验结果表明,该仪器的棉层检测速度达到40 m/h,识别精度达到90%.     

Dental neuroplasticity,neuro-pulpal interactions,and nerve regeneration

This review covers current information about the ability of dental nerves to regenerate and the role of tooth pulp in recruitment of regenerating nerve fibers. In addition, the participation of dental nerves in pulpal injury responses and healing is discussed, especially concerning pulp regeneration and reinnervation after tooth replantation. The complex innervation of teeth is highly asymmetric and guided towards specific microenvironments along blood vessels or in the crown pulp and dentin. Pulpal products such as nerve growth factor are distributed in the same asymmetric gradients as the dentinal sensory innervation, suggesting regulation and recruitment of those nerve fibers by those specific factors. The nerve fibers have important effects on pulpal blood flow and inflammation, while their sprouting and cytochemical changes after tooth injury are in response to altered pulpal cytochemistry. Thus, their pattern and neuropeptide intensity are indicators of pulp status, while their local actions continually affect that status. When denervated teeth are injured, either by pulp exposure on the occlusal surface or by replantation, they have more pulpal necrosis than occurs for innervated teeth. However, small pulp exposures on the side of denervated crowns or larger lesions in germ-free animals can heal well, showing the value of postoperative protection from occlusal trauma or from infection. Current ideas about dental neuroplasticity, neuro-pulpal interactions, and nerve regeneration are related to the overall topics of tooth biomimetics and pulp/dentin regeneration.     

On the processing and morphological aspects of metal fibers based on low-speed multi-tooth dry cutting

This study presents an investigation on both the processing and morphological aspects of cutting-based metal fibers. A self-designed multi-tooth cutter is used to efficiently make continuous long fibers under a low-speed dry-cutting condition. A finite element method-aided analysis is conducted to elucidate the mechanisms of this method. Based on both simulated and experimental results, it is found that fiber morphology shows different characteristics when different processing parameters are used. Moreover, the fiber structure and appearance also significantly depends on the mechanical properties of raw materials. It is shown that the Cu fiber belongs to flow chip due to highly plastic deformation, while the hardened Cu–Be, Cu–Be–Ni alloy and SUS316L fibers exhibit fractured features. The combined segmented vertical fins and sawtooth structures can be periodically formed on the Cu–Be fibers under an appropriate condition. Besides these findings, the effects of sintering condition on the fiber morphology are also reported in this work.     

Mesopic state: cellular mechanisms involved in pre- and post-synaptic mixing of rod and cone signals

At least twice daily our retinas move between a light adapted, cone-dominated (photopic) state and a dark-adapted, color-blind and highly light-sensitive rod-dominated (scotopic) state. In between is a rather ill-defined transitional state called the mesopic state in which retinal circuits express both rod and cone signals. The mesopic state is characterized by its dynamic and fluid nature: the rod and cone signals flowing through retinal networks are continually changing. Consequently, in the mesopic state the retinal output to the brain contained in the firing patterns of the ganglion cells consists of information derived from both rod and cone signals. Morphology, physiology, and psychophysics all contributed to an understanding that the two systems are not independent but interact extensively via both pooling and mutual inhibition. This review lays down a rationale for such rod-cone interactions in the vertebrate retinas. It suggests that the important functional role of rod-cone interactions is that they shorten the duration of the mesopic state. As a result, the retina is maintained in either in the (rod-dominated) high sensitivity photon counting mode or in the second mode, which emphasizes temporal transients and spatial resolution (the cone-dominated photopic state). Experimental evidence for pre- and postsynaptic mixing of rod and cone signals in the retina of the clawed frog, Xenopus, is shown together with the preeminent neuromodulatory role of both light and dopamine in controlling interactions between rod and cone signals. Dopamine is shown to be both necessary and sufficient to mediate light adaptation in the amphibian retina.     

Amacrine cells of the anuran retina: morphology, chemical neuroanatomy, and physiology

Amacrine cells are third-order retinal interneurons, projecting their processes into the inner plexiform layer. Historically, they were not considered as neurons first. By the middle of the 20th century, their neuronal nature was confirmed, and their enormous diversity established. Amacrine cells have been most successfully subdivided into morphological categories based on two parameters: diameter of the dendritic field and ramification pattern in the inner plexiform layer. Works combining anatomy, physiology, and neurochemistry are scarce and in the case of the anuran retina, the situation is even worse. Correlation between morphology, neurochemistry, and physiology is little studied. Here we try to build up a database and pinpoint some of the missing data. Obtaining those could help to better understand retinal function. Sporadic attempts did not make it possible to develop a comprehensive catalog of morphologically distinct amacrine cell types in the anuran retina. The number of morphologically identified amacrine cells currently stands at 16. The list of neurochemically identified distinct cell types can be given as follows: five types GABA-containing cell types with secondary markers and at least one without; two glycinergic cell types and one interplexiform cell where glycine colocalizes with somatostatin; one dopaminergic amacrine cell and also a variant of this with interplexiform morphology; two types of serotoninergic cells; three NADPHdiaphorase-positive cells, one substance P-positive cell type without identified second marker; one CCK-positive cell type without identified second marker and the calbindin positive cells (at least one but potentially more types). This adds up to 19 cell types, out of which two are interplexiform in character. This is more than that could be identified by purely morphological means. Out of Cajal's original 13 amacrine cell types described in the frog retina, 5 parallel unequivocally with neurons defined by neurochemistry. Three others have one close match each, but their exact identity is uncertain. The remaining amacrine cells have more than one potential matches. At the same time, on one hand the amacrine cell named two-layered by Cajal so far has no match among the neurochemically identified amacrine cells. On the other hand, the interplexiform subtype of the dopaminergic cell, the somatostatin-containing glycinergic interplexiform cell, the starburst cell, and the bistratified neuropeptide Y-immunoreactive cell have no match among Cajal's cells. All in all, the number of known amacrine and interplexiform cells now stands at at least 21 in the anuran retina. Physiological characterization of amacrine cells shows that their general features seem to be rather similar to those described in tiger salamander retina. In Xenopus retina, morphologically and physiologically identified amacrine cells responded to light stimulation most frequently with ON-OFF characteristics. Immunhistochemical identification of the recorded and dye injected cells showed that amacrine cells of the "same physiological type" might have different morphology. In other words, amacrine cells with different morphology can respond similarly to illumination. Even so, small differences between almost identical responses may reflect that the cell they stem from indeed belongs to different cell types.     

视网膜细胞显微镜的照明系统

为满足视网膜细胞成像照明光束的高亮度、窄谱宽要求,提出了一种用于视网膜细胞成像的照明系统,将半导体激光器发出的632.8nm激光耦合到芯径为105μm的多模光纤中,用聚光镜将多模光纤的出光端汇聚到一个旋转毛玻璃上,再用一个投射物镜将毛玻璃上的光源像投射到眼睛里照亮视网膜。试验发现该照明方法很好地消除了激光散斑,满足视网膜显微成像对高亮度光源的要求,光源有较窄的谱宽,成像系统色差很小,成像质量优于采用传统氙灯做照明光源的图像。该照明系统能较好地满足视网膜显微成像。     

保偏光纤应力自动测量装置

本文阐述应力型保偏光纤应力测量的原理和方法，即所谓光测弹性ＣＴ技术。简单介绍基于光测弹性ＣＴ技术研制成的应力自动测量装置，以及用这种装置对一种Ｂｏｗ—Ｔｉｅ保偏光纤的测量结果。     

Automated techniques for blood vessels segmentation through fundus retinal images: A review

Retina is the interior part of human's eye, has a vital role in vision. The digital image captured by fundus camera is very useful to analyze the abnormalities in retina especially in retinal blood vessels. To get information of blood vessels through fundus retinal image, a precise and accurate vessels segmentation image is required. This segmented blood vessel image is most beneficial to detect retinal diseases. Many automated techniques are widely used for retinal vessels segmentation which is a primary element of computerized diagnostic systems for retinal diseases. The automatic vessels segmentation may lead to more challenging task in the presence of lesions and abnormalities. This paper briefly describes the various publicly available retinal image databases and various machine learning techniques. State of the art exhibited that researchers have proposed several vessel segmentation methods based on supervised and supervised techniques and evaluated their results mostly on publicly datasets such as digital retinal images for vessel extraction and structured analysis of the retina. A comprehensive review of existing supervised and unsupervised vessel segmentation techniques or algorithms is presented which describes the philosophy of each algorithm. This review will be useful for readers in their future research.     

Fiber Traction Printing: A 3D Printing Method of Continuous Fiber Reinforced Metal Matrix Composite

A novel metal matrix composite freeform fabrication approach, fiber traction printing(FTP), is demonstrated through controlling the wetting behavior between fibers and the matrix. This process utilizes the fiber bundle to control the cross-sectional shape of the liquid metal, shaping it from circular to rectangular which is more precise. The FTP process could resolve manufacturing diffculties in the complex structure of continuous fiber reinforced metal matrix composites. The printing of the first layer monofilament is discussed in detail, and the effects of the fibrous coating thickness on the mechanical properties and microstructures of the composite are also investigated in this paper. The composite material prepared by the FTP process has a tensile strength of 235.2 MPa, which is close to that of composites fabricated by conventional processes. The complex structures are printed to demonstrate the advantages and innovations of this approach. Moreover, the FTP method is suited to other material systems with good wettability, such as modified carbon fiber, surfactants, and aluminum alloys.     

The ultrastructure of neuronal-pinealocytic interconnections in the monkey pineal.

Recent ultrastructural studies of neuronal-pinealocytic interconnections in the monkey pineal are reviewed. The pinealocytes in the adult monkey show almost all of the cytological specializations known in subprimate mammals. Adjacent pinealocytes are functionally coupled through ribbon synapses on cell bodies and gap junctions on cell bodies and cell processes. The pinealocytes receive direct synpatic contacts of nerve fibers with cholinergic terminal morphology. Nerve cells restricted to the central portion of the pineal receive synaptic contacts with more than three different morphologically defined types of nerve terminals. In addition to nerve terminals containing small clear vesicles or vesicles of pleomorphic morphology, a pinealocyte's terminal process containing the synaptic ribbon forms a true synaptic contact on the nerve cell body. The diversity of synapses on these nerve cells strongly suggests multiple origins of these neurons rather than a single peripheral parasympathetic origin. The possible involvement of pineal neurons in an intrinsic circuit that regulates the function of pinealocytes and integrates the neural input from the central as well as the peripheral nervous systems is discussed.