Nonolfactory sensory pathway to the telencephalon in a teleost fish.

Pathways conveying lateral-line sensory information within the brain of a bullhead catfish terminate in a localized zone within the telencephalon. Thus, the telencephalon in teleosts, as in amniote species, contains regions that receive specific sensory input. Therefore, this lemniscal organization is not restricted to mammalian or amniote species but is a feature common to most, if not all, vertebrates.

GAP-43 is critical for normal targeting of thalamocortical and corticothalamic, but not trigeminothalamic axons in the whisker barrel system.

Mice lacking the growth-associated protein GAP-43 (KO) show disrupted cortical topography and no barrels. Whisker-related patterns of cells are normal in the KO brainstem trigeminal complex (BSTC), while the pattern in KO ventrobasal thalamus (VB) is somewhat compromised. To better understand the basis for VB and cortical abnormalities, we used small placements of DiI to trace axonal projections between BSTC, VB, and barrel cortex in wildtype (WT) and GAP-43 KO mice. The trigeminothalamic (TT) pathway consists of axons from cells in the Nucleus Prinicipalis that project to the contralateral VB thalamus. DiI-labeled KO TT axons crossed the midline from BSTC and projected to contralateral VB normally, consistent with normal BSTC cytoarchitecture. By contrast, the KO thalamocortical axons (TCA) projection was highly abnormal. KO TCAs showed delays of 1-2 days in initial ingrowth to cortex. Postnatally, KO TCAs showed multiple pathfinding errors near intermediate targets, and were abnormally fasciculated within the internal capsule (IC). Interestingly, most individually labeled KO TCAs terminated in deep layers instead of in layer IV as in WT. This misprojection is consistent with birthdating analysis in KO mice, which revealed that neurons normally destined for layer IV remain in deep cortical layers. Early outgrowth of KO corticofugal (CF) axons was similar for both genotypes. However, at P7 KO CF fibers remained bundled as they entered the IC, and exhibited few terminal branches in VB. Thus, the establishment of axonal projections between thalamus and cortex are disrupted in GAP-43 KO mice.

Histomorphometric evaluation of mechanoreceptors and free nerve endings in human lateral ankle ligaments.

INTRODUCTION: Joint mechanoreceptors have been studied and most of investigators recognize the potential role of mechanoreceptors in the proprioceptive function of joint. The aim of this study was to analyze the general innervation and the possible existence of sensory receptors in the lateral ankle ligament. METHODS: Lateral ankle ligaments including anterior talofibular, posterior talofibular and calcaneofibular were obtained from 24 ankles of 13 male cadavers with ages ranging from 18 to 65 (mean 41.6) years. Each ligament was divided into three parts according to the bony attachments (proximal, central, and distal segments). Histologically mechanoreceptors (Ruffini, Pacini and Golgi) and free nerve endings were identified, and classified. Histomorphometric determination and evaluation of the density of the area of the receptor was performed by the point-counting methods. RESULTS: The anterior talofibular, posterior talofibular, and calcaneofibular ligaments were endowed with mechanoreceptor and free nerve endings. There was a significant prevalence of Pacini (p<0.001) compared with Ruffini and Golgi. However, there was no significant difference in the mechanoreceptors density in the different ligaments analyzed (p>0.05) CONCLUSION: Innervation of the lateral ankle ligaments was confirmed in this study, suggesting that the presence of mechanoreceptors could have clinical implication as well as relevance in the proprioceptive function. Future electrophysiological studies will be required to define the role in the proprioceptive and nociceptive system of the ankle.

Development of Johnston's organ in Drosophila.

Hearing is a specialized mechanosensory modality that is refined during evolution to meet the particular requirements of different organisms. In the fruitfly, Drosophila, hearing is mediated by Johnston's organ, a large chordotonal organ in the antenna that is exquisitely sensitive to the near-field acoustic signal of courtship songs generated by male wing vibration. We summarize recent progress in understanding the molecular genetic determinants of Johnston's organ development and discuss surprising differences from other chordotonal organs that likely facilitate hearing. We outline novel discoveries of active processes that generate motion of the antenna for acute sensitivity to the stimulus. Finally, we discuss further research directions that would probe remaining questions in understanding Johnston's organ development, function and evolution.

Structure and development of free neuromasts in barramundi, Lates calcarifer (Block).

This study was conducted to clarify the development of free neuromasts with growth of the barramundi, Lates calcarifer. A pair of free neuromasts was observed behind the unpigmented eyes in newly hatched eleutheroembryos with a mean total length of 1.93 mm, and two-hour-old eleuthero-embryos could respond to an approaching pipette. At 2 days after hatching, the egg yolk sac was mostly consumed, the eyes were pigmented, and the larvae commenced feeding on rotifers. Free neuromasts increased in number with growth and commenced developing into canal neuromasts in barramundi 15 days old with a mean total length of 8.07 mm. The average length of the major axis of the trunk free neuromasts attained approximately 12.9-15.5 microm, and the number of sensory cells was 15.4-17.5 at 15-20 days old. Developed cupulae of free neuromasts were observed in 1-day-old eleutheroembryos. The direction of maximum sensitivity of free neuromasts, determined from the polarity of the sensory cells, coincided with the minor axis of the lozenge-shaped outline of the apical surface of the free neuromasts. The polarity of trunk neuromasts was usually oriented along the antero-posterior axis of the fish body, but a few had a dorso-ventral direction. On the head, free neuromasts were oriented on lines tangential to concentric circles around the eye.

Morphology and physiology of the prosternal chordotonal organ of the sarcophagid fly Sarcophaga bullata (Parker).

The anatomy and the physiology of the prosternal chordotonal organ (pCO) within the prothorax of Sarcophaga bullata is analysed. Neuroanatomical studies illustrate that the approximately 35 sensory axons terminate within the median ventral association centre of the different neuromeres of the thoracico-abdominal ganglion. At the single-cell level two classes of receptor cells can be discriminated physiologically and morphologically: receptor cells with dorso-lateral branches in the mesothoracic neuromere are insensitive to frequencies below approximately 1 kHz. Receptor cells without such branches respond most sensitive at lower frequencies. Absolute thresholds vary between 0.2 and 8m/s(2) for different frequencies. The sensory information is transmitted to the brain via ascending interneurons. Functional analyses reveal a mechanical transmission of forced head rotations and of foreleg vibrations to the attachment site of the pCO. In summed action potential recordings a physiological correlate was found to stimuli with parameters of leg vibrations, rather than to those of head rotation. The data represent a first physiological study of a putative predecessor organ of an insect ear.

Chemosensory coding by neurons in the coeloconic sensilla of the Drosophila antenna.

Odor coding is based on the diverse sensitivities and response properties of olfactory receptor neurons (ORNs). In the Drosophila antenna, ORNs are housed in three major morphological types of sensilla. Although investigation of the Drosophila olfactory system has been expanding rapidly, the ORNs in one of these types, the coeloconic sensilla, have been essentially unexplored. We define four functional types of coeloconic sensilla through extracellular physiological recordings. Each type contains at least two neurons, with a total of at least seven distinct ORN classes that vary remarkably in their breadth of tuning. Analysis of 315 odorant-ORN combinations reveals how these neurons sample odor space via both excitation and inhibition. We identify a class of neurons that is narrowly tuned to small amines, and we find humidity detectors that define a cellular basis for hygroreception in Drosophila. The temporal dynamics of responses vary widely, enhancing the potential for complexity in the odor code. Molecular and genetic analysis shows that a broadly tuned ORN, antennal coeloconic 3B (ac3B), requires the odor receptor gene Or35a for its response in vivo. The activity of ac3B is not required for the response of the other ORN within that sensillum, ac3A. The functional analysis presented here, revealing a combination of highly specialized neurons and a broadly tuned ORN, along with the ancient origin of coeloconic sensilla, suggests that the specificities of these ORNs may reflect basic needs of an ancestral insect.

Feeling the vibes: chordotonal mechanisms in insect hearing.

To hear, insects use diverse external structures, which transform acoustic signals to mechanical ones, coupled to astonishingly uniform mechanosensory transducers, the chordotonal organs. New evidence showing that chordotonal organs and vertebrate auditory hair cells are developmentally related and that chordotonal organs and insect bristle organs are mechanistically related suggests that all these ciliated mechanoreceptors may be derived from the same ancestral molecular mechanotransduction complex. Identification of these elusive molecules will settle this issue.

Nerve endings of the wrist joint: a preliminary report of the dorsal radiocarpal ligament.

As part of an investigation of the articular nerve ending populations in the wrist joint capsule associated with the anterior and posterior interosseous nerves, this study addresses the nerve ending population in the dorsal radiocarpal ligament. The ligaments were harvested from four wrists of two fresh cadavers within 12 h of death. Tissues were fixed, cryostat sectioned, and processed for fluorescence immunohistochemistry using antibody to protein gene product 9.5 (PGP 9.5), a general or pan neuronal marker, and a secondary antibody conjugated to a fluorescent tag (Alexa Fluor 488). The sections were evaluated with a confocal laser microscope and an image analyzer. Labeled nerve endings were mapped, measured, and categorized. Type I (Ruffini-like ending), Type III (Golgi-like tendon organ) and Type IV (noncorpuscular) nerve endings could be identified in all four DRC ligaments, with Types I and IV dominating. These receptors were distributed primarily over the superficial two thirds of the ligament (>80%), and near the bony attachments (>70%). The dorsal radiocarpal ligament has a rich sensory innervation from the posterior interosseous nerve terminating in nerve endings located in the superficial two-thirds of the ligaments, primarily near bony attachment sites.

Neural coding of the location and direction of a moving object by a spatially distributed population of mechanoreceptors.

A neural code for the location and direction of an object moving over the fingerpad was constructed from the responses of a population of rapidly adapting type I (RAs) and slowly adapting type I (SAs) mechanoreceptive nerve fibers. The object was either a sphere with a radius of 5 mm or a toroid with radii of 5 mm on the major axis and either 1 or 3 mm on the minor axis. The object was stroked under constant velocity and contact force along eight different linear trajectories. The spatial locations of the centers of activity of the population responses (PLs) were determined from nonsimultaneously recorded responses of 99 RAs and 97 SAs with receptive fields spatially distributed over the fingerpad of the anesthetized monkey. The PL at each moment during each stroke was used as a neural code of object location. The angle between the direction of the trajectory of the PL and mediolateral axis was used to represent the direction of motion of the object. The location of contact between the object and skin was better represented in SA than in RA PLs, regardless of stroke direction or object curvature. The PL representation of stroke direction was linearly related to the actual direction of the object for both RAs and SAs but was less variable for SAs than for RAs. Both the SA and RA populations coded spatial position and direction of motion at acuities similar to those obtained in psychophysical studies in humans.

Differences in the presence of mechanoreceptors and nerve structures between wrist ligaments may imply differential roles in wrist stabilization.

The purpose of this study was to analyze human wrist ligaments with regard to presence of general innervation and mechanoreceptors. The ligaments studied were: dorsal radiocarpal (DRC), dorsal intercarpal (DIC), long radiolunate (LRL), radioscaphocapitate (RSC), ulnocarpal (UC), scapholunate interosseous (SLI) and lunotriquetral interosseous (LTI) ligaments. Specific immunohistochemical markers were used to target neural/perineurial structures. Both Ruffini and Pacini-like mechanoreceptors (sensory corpuscles) as well as nerve fascicles/free nerve fibers were identified. Ruffini corpuscles were primarily identified via their dendritic intracapsular nerve endings, whereas the Pacini-like corpuscles were identified through their thick perineurial capsules with marked p75 immunoreaction. The wrist ligaments were found to vary in innervation, the DIC, DRC and SLI being richly innervated, whereas the LRL being almost without innervation. The difference in innervation between the ligaments might reflect differential function. Ligaments without innervation might act as structures of passive restraint, whereas ligaments with rich innervation are proposed to also provide proprioceptive information. Wrist ligament injuries should, therefore, be regarded as a disturbance not only of the intrinsic carpal kinematics, but also of the coordination and proprioception of the entire wrist joint.

The Haarscheibe.

The Haarscheibe is a specialized spot of epidermis containing many Merkel cell-neurite complexes. It is a highly sensitive, slowly adapting, modality-specific touch receptor occurring in all mammals. Its exact role in signaling sensation in human beings is undetermined, and the function of Merkel cells, with their distinctive cytoplasmic granules, in transducing mechanical force into neural action potentials remains to be determined.

A comparison of the Eimer's organs of three North American moles: the hairy-tailed mole (Parascalops breweri), the star-nosed mole (Condylura cristata), and the eastern mole (Scalopus aquaticus).

Eimer's organ is a tactile sensory structure found predominantly on the snouts of moles. It consists of a raised papilla of epidermis containing a column of cells associated with sensory receptors. This study compares the Eimer's organs of the hairy-tailed mole, Parascalops breweri, the star-nosed mole, Condylura cristata, and the eastern mole, Scalopus aquaticus, by using scanning electron microscopy and light microscopy. Eimer's organs are visible on the snout of the hairy-tailed and the star-nosed moles, but not the eastern mole. The Eimer's organs of the hairy-tailed mole are similar in external appearance, distribution, and internal structure to those found in most species examined. The Eimer's organs of the star-nosed mole and the eastern mole diverge from this basic form in seemingly opposite directions. The Eimer's organs of the star-nosed mole are more numerous, smaller, and highly organized units with a consistent pattern of neuronal terminal swellings within a cell column, below a thin keratinized epidermis. By contrast, the Eimer's organs of the eastern mole lie below a thick keratinized epidermis, are less organized in structure, and have no central cell column. The extreme differences between the Eimer's organs of the star-nosed mole and thos of the eastern mole may be the result of the habitat of each species, saturated mud allowing a more elaborate and delicate sensory apparatus in the star-nosed mole and drier soil requiring a thick keratinized epidermis over the organ in the eastern mole.

Sensory nerve endings in rhesus monkey sinus hairs.

The sensory innervation of primate sinus hairs has been studied by light and electron microscopy. For light microscopy paraffin sections as well as thick frozen sections were impregnated with silver and compared with serial semi-thin sections of tissue prepared for electron microscopy. One type of sensory terminal is present in the epidermis surrounding the hair follicle, and four specific nerve terminals have been identified within the blood sinus. An epidermal rete ridge collar encircles the hair shaft and contains approximately 200 Merkel cell-neurite complexes. Numerous other Merkel cell-neurite complexes are present in the external root sheath of the hair follicle beneath a thick glassy membrane innervated by approximately 65 nerve fibers. At this level 10-15 lanceolate or palisade terminals are situated in the connective tissue. Up to 10 simple encapsulated corpuscles can be identified above the level of lanceolate endings and Merkel cell terminals. Ruffini corpuscles are closely applied to the glassy membrane below the lanceolate and Merkel terminals at the level where nerve fibers penetrate the capsule of the sinus. All of these terminals are supplied by 80-100 large diameter myelinated fibers distributed approximately as follows: 65 innervate Merkel cell-neurite complexes, 15 to lanceolate, 10 to simple corpuscles, and 10 to Ruffini corpuscles. The innervation of the rete ridge collar is independent of that of the sinus consisting of 10-12 fibers derived from the superficial dermal network. Each of these sensory terminals can be correlated with specific functional parameters as described in numerous neurophysiologic studies. Merkel cell-neurite complexes and Ruffini corpuscles ae slowly adapting receptors; lanceolate terminals and simple corpuscles are rapidly adapting receptors.

Projection and local interneurons in the sixth abdominal ganglion of the sand crab Emerita analoga (Hippidae).

Hippid crabs are adapted for life in the surf zone of exposed sandy beaches, and their tailfan differs from the tailfans of other crustaceans with respect to morphology and motor control and in having nonspiking stretch receptors (NSR). To investigate how these crabs' mechanosensory systems are adapted to this turbulent environment, I used axonal back-filling and intracellular recording with dye-filled microelectrodes to describe afferent projections from the telson and morphologies and physiological responses of intersegmental and local neurons in abdominal ganglion 6 (A6) in Emerita analoga, then compared them with descriptions of corresponding neurons in A6 of crayfish. The density of afferent terminals and the proportion of projection neuron somata is lower in anterior A6 of E. analoga than in crayfish, perhaps correlated with a reduction in hydrodynamic setae. Many interneurons responded to afferent nerve stimulation and displayed activity correlated with levels of A6 motor output. NSR stretch depolarizes unilateral local neurons and terminals of axons entering A6 from the connective and hyperpolarizes bilateral local and projection neurons. The timing and duration of this inhibition would suppress mechanosensory input from the telson during uropod beating (homologue of crayfish's nongiant tail-flipping). Suppression of reafference during uropod beating may have been pivotal for evolution of hippids' ability to move rapidly across the water-sand interface in the slosh zone of sandy beaches. Homologies between A6 neurons in E. analoga and crayfish, suggested by morphological and physiological similarities, indicate that the NSRs connect to a neuronal network regulating exteroceptive input that was inherited from their tail-flipping ancestors.

The distribution of commissural terminations in somatosensory areas I and II of the grey squirrel.

The topographic distribution of somesthetic interhemispheric projections was studied in grey squirrels using the Fink-Heimer technique following large aspiration lesions of the corpus callosum. On the day of perfusion, receptive fields were determined for microelectrode recording sites in the first, S I, and second, S II, somatosensory areas of cortex, and small electrolytic lesions were made in order to identify some of these sites in prepared brain sections. The cortex was then separated from the rest of the brain, flattened, and cut parallel, so that with the aid of the reference lesions, the total pattern of degeneration could be related to a surface view of the brain and to previous electrophysiological maps of S I (Sur et al., '78) and S II (Nelson et al., '79). The results show that callosal terminations are unevenly distributed in S I and S II, and suggested that there are several categories of callosal inputs to S I. A major region of terminations is in the architectonically distinct "unresponsive zone" within SI, and perhaps in other similar, but narrower, specialized zones within and bordering S I, as previously described in rats (Ryugo and Killackey, '75; Wise and Jones, '76, '78; Akers and Killackey, '78). Other callosal projections terminate within the responsive regions of S I. These regions include at least some of the representation of the body midline, most clearly the midline of the representations of the upper and lower face, as well as regions unrelated to the midline of the body. Most of all of the S I cortex responsive to stimuli away from the midline on the upper and lower lips, the mystacial vibrissae, and the glabrous forepaw was almost free of direct callosal terminations. Except for a central core region, most of S II appears to receive a moderate distribution of callosal inputs.

Topographic inventories of vagal afferents in gastrointestinal muscle.

To inventory and characterize the two types of vagal afferents (both putative mechanoreceptors) in the muscle of the gastrointestinal tract, the authors injected wheat germ agglutinin-horseradish peroxidase into the nodose ganglia of rats that had received unilateral ventral rhizotomies to eliminate efferents. The gut, from the oral esophagus to the distal colon, was divided into wholemounts, processed with tetramethylbenzidine, and surveyed to establish normative topographic maps of afferents. Vagal intraganglionic laminar endings (IGLEs) were ubiquitous, with concentrations varying on a longitudinal gradient (higher rostrally). This overall gradient was punctuated by denser condensations of endings in the oral esophagus, gastric corpus, and distal ileum. In regional specializations, IGLEs were fused into conspicuous, dense networks in the laryngeal esophagus and the antrum. Intramuscular arrays (IMAs) had restricted distributions, including the walls of the stomach and the sphincters throughout the gut. In the forestomach, a singular concentration of orthogonally crossed IMAs was organized into a lattice or "fovea." IMAs displayed variations in morphology, with one specialization consisting of short, terminal processes associated with sphincters and a more widespread form consisting of long, rectilinear processes in the forestomach, along the greater curvature, and in limited intestinal regions. On the basis of their topographic patterns and structural specializations, the two putative mechanoreceptors may have different functions: IGLEs appear situated to integrate intramural tension, and perhaps myenteric neuronal activity, into rhythmical, propagated motor programs, such as swallowing, peristalsis, and emptying. IMAs are distributed strategically and appear to satisfy structural requirements for stretch receptors tuned to tonic or more aperiodic events that may affect central nervous system processing as well as local gastrointestinal coordination.

A topographic map of sensory cell terminal arborizations in the cricket CNS; correlation with birthday and position in a sensory array.

The development of a group of club-shaped sensilla called clavate hairs, located on the cerci of the cricket (Acheta domesticus), was examined morphologically. The clavate hairs are located on the base of the cercus and are thought to inform the animal of its orientation with respect to gravity. There are two groups of clavate hairs distinguished from one another by the orientation of their sockets: a dorso-medial group whose sockets are oriented perpendicular to the long axis of the cercus and a ventro-medial group inclined 45-60 degrees away from the perpendicular. The ventro-medial group consists of a series of rows of sensilla running parallel to the long axis of the cercus. By examining a cast-off exoskeleton in the scanning electron microscope and comparing it with newly developed cuticle of the subsequent instar (Fig. 3), we showed how receptors were added to the ventro-medial array of clavate hairs. The first ventral hair (#10,Fig.1) appeared in the second instar. Three more hairs were added in the third instar: two (#11 and #12) proximal to hair 10 forming the first row and one (#20) medial to 11 and initiating the second row. After the third instar on hair was usually added proximal to each row each time the specimen molted. Because of the regular positioning of hairs and their orderly addition to the array, it is possible to identify uniquely all of the hairs in the three largest rows of ventral hairs (Fig. 4). We developed a simple method for staining the neuron associated with each hair. A hair was injured by cutting off its tipe. A bubble of cobaltous acetate was then placed on the hair for 18-20 hours and only the neuron associated with the injured hair took up the stain. The synaptic terminal aborizations of identified neurons examined in this manner were unique and reproducible from specimen to specimen (Fig.6). Furthermore, there is a topographic order to the terminal aborizations. Within one row the oldest neurons project furthest into the nervous system and arborize over the greatest area, whereas younger neurons aborize in more restricted areas nwer the entrance of the cercal nerve. Thus it was concluded that birthday was correlated with the morphology of the synaptic aborization. By staining neurons that were the same age but located in different rows, we determined that birthday was not the only variable influencing the morphology of the terminal arbors. The terminal arbors of neurons 11 and 20, both of which first appear in the third instar, were very different from one another. Thus another variable, presumably position on the body surface, was also correlated with the morphology of a neuron's terminal arborization. We concluded from these results that position on the cercus as well as birthday is encoded in the devlopmental program of these neurons and that the morphology of their terminal arborizations is a joint junction of these two variables.

Second somatic sensory area in the cerebral cortex of cats: somatotopic organization and cytoarchitecture.

The cortex of the anterior ectosylvian gyrus and adjoining ectosylvian and suprasylvian sulci was explored with tungsten microelectrodes to determine the distribution of responses to light cutaneous stimulation in barbiturate-anesthetized cats. Recordings were spaced between 125 and 250 micrometers and, in several cases, nearly all of the somatic areas in this cortex were explored in the same brain. Four somatic sensory areas were identified on the basis of responses properties, sequences of receptive fields, and cytoarchitecture. The largest area, which occupied the rostral and medial two-thirds to three-fourths of the exposed, relatively flat portion of the anterior ectosylvian gyrus, was called the second somatic sensory area (SII). Receptive fields in SII were primarily from the contralateral side of the body; they were well defined and somatotopically organized into an erect representation of the body. The top of the head was located next to a similar representation of the periphery in a portion of the first somatic sensory area (SI). Individual distal digits and toes occupied discrete components of the SII map. Another representation for the distal forelimb and hindlimb was noted medially along the lateral bank of the anterior suprasylvian sulcus. Receptive fields and response properties in this region were equivalent to those seen in SII proper. However, only a crude anteroposterior, fore- to hindlimb topographical organization was noted, but with more distal parts of the limbs generally located closer to the fundus of the sulcus in this medial representation. As the cytoarchitecture in this medial region was similar to the rest of SII it was considered a medial subdivision of SII. A third, topographically organized zone was located lateral to SII largely within the upper bank of the anterior ectosylvian sulcus and adjoining lateral crest of the anterior ectosylvian gyrus. Large, stockinglike, contralateral receptive fields were common; ipsilateral components to the receptive fields were present. Some individual digit receptive fields were located in the rostral part of the forelimb zone within the anterior ectosylvian sulcus. This lateral somatic area is probably equivalent to a fourth somatic sensory area (SIV) recently identified by Clemo and Stein ('82). Posterior to the hindlimb zones of SII and medial to SIV was another region that responded to cutaneous plus auditory stimulation. There was no detectable topography in this area; nearly all of the receptive fields were large, frequently bilateral, and often involved the whole body or all four extremities. This area's cytoarchitecture was comparable to previous descriptions of the suprasylvian fringe (Rose, '49). The location and physiology of these four areas were discussed in reference to previous controversies regarding the topography of the body representation in SII and the location of an acallosal zone in this region of cortex.

Somatotopic organization of vibrissae afferents in the trigeminal sensory nuclei of the rat studied by transganglionic transport of HRP.

Transganglionic transport of horseradish peroxidase (HRP) has been used to study the cell bodies and central projections of neurons innervating the vibrissae in the rat. These can be grouped into five horizontal rows and one posterior vertical row. Twenty-four to 48 hours after the nerves innervating different vibrissae were exposed to HRP, the trigeminal ganglia, brainstem, and upper cervical spinal cord were fixed by perfusion and serial sections were processed according to the tetramethylbenzidine technique. The results revealed a tendency for somatotopic organization in the trigeminal ganglion of cell bodies innervating the different vibrissae. Corresponding termination areas in the trigeminal sensory nuclei showed a detailed pattern of organization replicating the peripheral organization of the vibrissae. In all trigeminal sensory nuclei the horizontal rows are represented in an inverted fashion from dorsal to ventral, i.e., the most dorsal row is represented most ventrally. In addition, the more anterior a vibrissa is located, the deeper is it represented in the rostral nonlaminated nuclei. The situation is reversed in the laminated nucleus caudalis. The posterior vertical row is represented most superficially in the rostral nonlaminated nuclei, but most deeply in the laminated nucleus caudalis. In nucleus caudalis there are also rostrocaudal differences in the representation of different vibrissae. Thus, the posterior vibrissae in a horizontal row have their main representations more caudally than the anterior vibrissae. The posterior vertical row has its main representation most caudally, in the C1 segment.