Developmental regulation of Fos-protein during proliferative growth of the otic vesicle and its relation to differentiation induced by retinoic acid.

This work studies Fos protein expression in the otic vesicle and the developing cochleovestibular ganglion (CVG), focusing on the possible role of Fos in the regulation of cell proliferation and differentiation during otic development. Fos was detected as a product of 56-62 kDa in otic vesicles and CVG lysates. Expression was transient and stage-dependent. Maximal levels occurred at stage 20 in the otic vesicle and at Day 4 in the CVG. Another wave of Fos expression occurred after Day 7 of development, out of the early proliferative period. Fos immunoreactivity was localized in cell nuclei of otic epithelium and CVG. Fos was readily induced by mitogens like serum and bombesin and this induction was inhibited by 25 nM retinoic acid, an inhibitor of cell proliferation in the otic vesicle.c-fos antisense oligonucleotides inhibited growth in the otic vesicle in parallel with a reduction in Fos expression. High levels of Fos protein were not sufficient, however, to sustain growth of isolated otic vesicles in the absence of mitogens. Incubation with retinoic acid (24 hr) induced differentiation of sensory hair-cells in parallel with inhibition of cell proliferation. Contrary to retinoic acid, Fos inhibition by antisense did not induce differentiation. The results suggest that Fos is part of the signaling mechanisms regulating normal development of the inner ear. Regulation of Fos may be required for controlling of the transition between cell proliferation and differentiation.

Immunohistochemical localization of the high-affinity NGF receptor (gp140-trkA) in the adult human dorsal root and sympathetic ganglia and in the nerves and sensory corpuscles supplying digital skin.

BACKGROUND: Nerve growth factor (NGF) is produced in target tissues of sympathetic and neural-crest derived sensory neurons, including skin, to provide them trophic support. The biological effects of NGF on responsive cells are mediated by specific high-affinity receptors. Recently, a protein tyrosine kinase of congruent to 140 kDa molecular weight, encoded by the proto-oncogene trkA, has been identified as the high-affinity NGF receptor (gp140-trkA). The present work was undertaken to study the localization of gp140-trkA-like immunoreactivity (IR) in human peripheral ganglia (sympathetic and dorsal root ganglia), and in glabrous skin. METHODS: Lumbar dorsal root ganglia, para- and prevertebral sympathetic ganglia, and digital glabrous skin were studied immunohistochemically using a rabbit anti-gp140-trkA polyclonal antibody. In order to accurately establish the localization of gp140-trkA IR, the neurofilament proteins and S-100 protein were studied in parallel in: (1) sensory and sympathetic ganglia, to label neuron cell bodies and satellite or supporting cells, respectively; (2) human skin, to label axons, Schwann and related cells within nerves and sensory corpuscles. Moreover, a quantitative study (neuron size, intensity of immunostaining) was carried out on sympathetic and dorsal root ganglia neuron cell bodies. RESULTS: A specific gp140-trkA-like IR was found in: (1) a subpopulation (65%) of primary sensory neuron cell bodies, including most of the large-sized ones but also small- and intermediate-sized ones; (2) most of sympathetic neuron cell bodies (82%); (3) the perineurial cell, Schwann cells, and large axons of the nerve trunks supplying digital skin; (4) the lamellar cells of Meissner corpuscles; (5) the central axon, inner-core, outer-core, and capsule of Pacinian corpuscles. In addition, the occurrence of gp140-trkA-like IR was observed in some non-nervous tissues of the skin, including epidermis (mainly in the basal layer), sweat glands, and arterial blood vessels. CONCLUSIONS: Present results provide evidence for the localization of gp140-trkA-like IR in: (1) nerve cells which are known to be NGF-responsive, and (2) non-nervous cutaneous tissues which are innervated by NGF-dependent peripheral neurons. These findings suggest that, in addition to the well-established role of NGF on sensory and sympathetic neurons, this neurotrophin may be able to regulate some other functions on non-nervous cells which are targets for NGF-dependent peripheral neurons.

beta-Amyloid precursor protein (APP)-like immunoreactivity in the human sympathetic ganglia.

The localization of the beta/A4 amyloid precursor protein (APP) was studied in the human lumbar paravertebral sympathetic ganglia of subjects of different ages, free of neurologic disease, using combined immunohistochemistry and image analysis techniques (optic microdensitometry). To ascertain which cells displayed APP-like immunoreactivity (APP-LI), S-100 and neurofilament proteins were studied in parallel to label the supporting glial cells and the neuron perikarya, respectively. Specific APP-LI was observed labelling both neuron cell bodies and supporting glial cells independently of age. In all cases, the intensity of immunostaining was stronger in glial cells than in neurons. Moreover, the intensity of APP-LI was independent of both age and neuron size. Present results provide evidence for the presence of APP-LI in the human sympathetic ganglia, and for the absence of changes in the expression of this protein, or proteins, with aging. The functional and clinical relevance of these findings remains to be clarified.

Expression of epidermal growth factor receptor (EGFr) immunoreactivity in human cutaneous nerves and sensory corpuscles.

BACKGROUND: The epidermal growth factor receptor (EGFr) binds both epidermal growth factor (EGF) and transforming growth factor alpha (TGF alpha), which are currently considered among putative growth factors playing a role in the nervous system. EGFr and their ligands have been localized in the mammalian peripheral nervous system. The present study was undertaken to investigate whether nerves and sensory corpuscles supplying human glabrous skin express EGFr. METHODS: Formaldehyde fixed, paraffin embedded samples of finger-tip digital skin obtained from adult healthy subjects were processed for indirect PAP immunohistochemistry using a monoclonal antibody against an epitope of the intracellular domain of EGFr. To ascertain the localization of EGFr immunoreactivity, neurofilament proteins (NFP), S100 protein (S100P), and epithelial membrane antigen (EMA) were studied in parallel to label axons, Schwann cells, and perineurial cells, respectively, as well as their corpuscular derivatives. RESULTS: A variable intensity of EGFr immunostaining was regularly observed in the perineurium and Schwann cells, and occasionally in the axons of nerve bundles. EGFr immunoreactivity was also present in the axon and lamellar cells of Meissner corpuscles, and within the axon, inner-core, outer-core, and capsule of Pacinian corpuscles. CONCLUSIONS: Present results demonstrate that human cutaneous nerves and sensory corpuscles express EGFr suggesting a role for peptides able to bind EGFr, i.e., EGF and TGF alpha, in the human peripheral nervous sensory system.

Morphological study by scanning electron microscopy of the lingual papillae in the common European bat (Pipistrellus pipistrellus).

There are many accounts of the tongues of mammals observed with scanning electron microscopy (SEM), but apparently only one article about the tongue of the Chiroptera. In the present study the tongue surface (after removing extracellular material) of the European common bat (Pipistrellus pipstrellus) was examined. The tongue is covered with papillae and has an elevation between its medial and posterior half. There are three types of papillae: filiform, fungiform and circumvallate, and the filiform can be classified as strictly filiform, conical and crown-like. The shapes and disposition of these papillae are related to function, which is principally to retain captured food during flight. At higher magnification the surface of the filiform papillae has many pores and microridges, which may serve for the production and distribution of mucus over the papillary surface.

Chondroitin sulphate proteoglycan and embryonic brain enlargement in the chick.

Previous studies of the early development of the neural tube have shown the existence of an intraneural fluid, which causes a positive pressure inside this primordium, and seems to play a key role in the early development of the central nervous system. In the present study we investigated the composition and synthesis of this intraneural fluid. By using a sequential method, which includes fixation with glutaraldehyde plus cetylpyridinium chloride, opening the neural cavity after critical point drying and scanning electron microscopy analysis, we found a water-soluble extracellular matrix that filled up the brain vesicles of chick embryos at the earliest stages of the neural tube. An ultrastructural study of the neural epithelium during these stages revealed the existence of a secretion process in the neural cells toward the apical side, the future neural cavity. An immunocytochemical study to assess the nature of the secreted material has shown that the intraneural matrix contains chondroitin sulphate proteoglycan, which appeared homogeneously distributed throughout the neural cavity. Our findings demonstrate that the intraneural liquid is a fluid of complex composition and includes chondroitin sulphate proteoglycan as an osmotically active molecule. This suggests a morphogenetic role for the proteoglycan during early brain enlargement. The neural ectoderm is a polarized epithelium from early developmental stages and secretes the intraneural matrix.

Patterns of epithelial cell death during early development of the human inner ear.

A light microscopic study of cell death in a developmental series of otic primordia from 23 human embryos (Carnegie stages 9 to 14) was completed. Degenerated cells were noted predominantly in the placode (stages 9 and 10), cup (stages 11 and 12), and otocyst (stages 13 and 14). A systematic camera lucida study of the appearance and topography of degenerating epithelial cells showed four different areas of cell death in the otic primordia that related to 1) invagination and detachment of the otic anlage, 2) early histogenesis of the statoacoustic ganglion, and 3) development of the endolymphatic duct. The possible role of cell death in the morphogenesis of the inner ear related to morphogenetic movements is discussed.

Bombesin and other growth factors activate cell proliferation in chick embryo otic vesicles in culture.

The ability of the mitogenic peptide bombesin and other growth factors to trigger and support early development of the inner ear was studied on chick embryo otocysts in culture. The normal pattern of development was preserved in cultured otic vesicles in the presence of 20% fetal calf serum in the medium. Differentiation proceeded from stage 18 to 22 during the first 24 h and further to stage 24 in 48 h. Estimates of cell number and mitotic rates revealed a distinct period of proliferative growth which was maximum at the 24 h period of incubation. This was coincident with a high rate of DNA synthesis as measured by the acid-precipitable incorporation of [3H]thymidine. Development could be arrested by deprivation of serum during 24h. It could then be reactivated by readmission of serum to proceed with the normal pattern of morphological differentiation and cell proliferation. Bombesin (100 nM) was able to reactivate development in growth-arrested vesicles. Its effect was dose-dependent, saturable and potentiated by insulin (5 micrograms ml-1) which was ineffective if used alone. When associated with insulin, bombesin carried differentiation to stage 21 and stimulated mitotic activity above the level of serum as judged from estimates of cell number and [3H]thymidine uptake. EGF and PDGF were also effective in reinitiating development although their potency was smaller than bombesin. The reactivation by serum or bombesin was blocked by amiloride. The results show that (1) the otic vesicle can provide a useful model for studying the mechanisms that control proliferative growth and differentiation during normal development and (2) bombesin and other growth factors are able to activate growth in embryonic developing tissues.

Protein kinase C activation is required during the early development of the inner ear in culture.

The role of protein kinase C (PKC). during the early development of the inner ear was investigated using organ culture techniques. Otocysts isolated from chick embryos were made quiescent by culturing in the absence of serum for 24 h. The normal process of development could be reactivated by restoration of serum and other growth factors. Addition of phorbol ester (TPA) or synthetic diacylglycerol (OAG) to serum-free medium was also effective in reactivating development and stimulation of DNA synthesis was 41% and 52% of that of serum, respectively. Insulin potentiated the effects of TPA and OAG but had no effect when present alone. Morphogenesis and the associated cell proliferation stimulated by either serum or PKC activation were both inhibited by sphingosine, an in vitro inhibitor of PKC. Inhibition by sphingosine was dose-dependent with a half-maximal inhibitory concentration of about 10 µM. The results suggest that PKC activation is an essential step in controlling proliferative growth during early stages of the development of the inner ear.

Polarization and density of Na-pumps in the inner ear of the chick embryo during early stages of development.

The otic vesicle consists of a pseudostratified epithelium with some features of transporting epithelia. The present work questions whether Na-pumps are polarized in this epithelium and what is the relation between the location or density of pumps and development. This was done by measuring the binding of [3H]ouabain to isolated otic vesicles in developmental stages 16 to 22. The results show the presence of specific ouabain-binding sites located in the inward-facing membrane of the otic vesicle epithelium. Binding was saturable at increasing concentrations of ouabain and was highly sensitive to the external K+ concentration with half-maximal inhibition below 0.5 mM, indicating that the binding sites and Na-pump sites are identical. A transient stage-dependent increase in the density of Na-pumps during the period that precedes growth was observed. Evidence is given against this being directly related to an increased net fluid transport rate despite the fact that pump sites were always polarized throughout these stages. The conclusions are that (1) the otic vesicle epithelium is a polarized structure with the possibility of vectorial transport of solutes and water and (2) the increased number of pumps may operate as a regulatory mechanism during normal proliferative growth.

Electrical properties of the otic vesicle epithelium in the chick embryo.

The electrophysiological properties of the epithelium of the otic vesicle were studied in the chick embryo using conventional microelectrode techniques. A preparation is described that allows continuous recording of transmural potential and resistance during changes in the composition of the bathing fluid. Vesicles in stages 18 to 22 showed a spontaneous transmural potential (ET) that ranged from 2 to 6 mV, inner positive. This electrical potential difference was abolished after 2 h incubation in K+-free strophantidin (10(-4) M) and it increased by about twofold immediately after addition of the cation ionophore Amphotericin B (250 microM) to the bath. The specific resistance of the wall (RT) was about 80 omega cm2 between stages 18 and 22 indicating a low-resistance, noncellular, permeation pathway for current flow. The short-circuit current, calculated from ET and RT was about 50 X 10(-6) A cm-2 throughout this period. This corresponds to a net flux of 187 X 10(-8) mol cm-2 h-1 of a single cation pumped towards the towards the vesicular cavity. Diffusion potentials (salt gradients and single-ion substitutions) showed a selectivity ratio PK:PNa:PCl = 1:0.9:0.7, which is that of a weakly charged aqueous pathway. Measurements of vesicular volume and surface area showed an increase by a factor of ten in the size of the vesicle with maximal rates of change in volume of 5 microliter cm-2 h-1. The electrical properties reported here for the epithelium of the otic vesicle resemble very much those of 'leaky' epithelia which are known to transport ions and water at a very high rate.