PubMed Health⌕ Search

Biomedical subjects

M S Davidoff

Publications and source records attributed to M S Davidoff.

At least 37 records · Page 2Linked to original sources

Vasopressin- and oxytocin-immunoreactive nerve cells in the aging rat hypothalamus.

Immunohistochemistry and morphometry were used to study the age-related changes in the vasopressin (AVP) and oxytocin (OXT) nerve cells in the paraventricular (PVN), supraoptic (SON) and suprachiasmatic (SCN) nuclei of 3-, 11- and 28-month-old rats. The results showed a statistically significant reduction in the mean number of AVP cells in the PVN, SON and SCN, and of OXT cells in the PVN with advancing age. Different age-related changes in the mean size of the immunoreactive cells were found in the three nuclei: a significant and transitory increase in the AVP and OXT cell sizes in the PVN, a tendency towards increasing the AVP and OXT cell sizes in the SON, and a significant and gradual decrease in the AVP cell size in the SCN. The combination of the morphometric data and staining patterns of the AVP and OXT perikarya and fibers in the PVN and SON pointed to an increased transport of AVP and OXT in 11-month-old rats as well as to a decreased production of these peptides in the PVN of 28-month-old rats. Taken together the staining pattern and the morphometric results showed a progressive loss of AVP cells in the SCN in aging.

Aging↗

Substance P modulating effect on the binding capacity of hamster Leydig cell LH receptors.

The influence of Substance P was studied on the binding characteristics of LH receptors in purified Leydig cells collected from golden hamsters kept under natural long or short days. Substance P exerted a differential effect on the binding capacity of LH receptors. A significant increase in Bmax was estimated in Leydig cells obtained from young hamsters living under long days. In contrast, Substance P reduced the number of the LH binding sites in Leydig cell cultures prepared from adult hamsters housed under short-day conditions.

Animals↗

Nitric oxide synthase (NOS-I) in Leydig cells of the human testis.

By means of immunocytochemical methods, immunoreactivity for the brain isoform of nitric oxide synthase (NOS-I) was recognized in numerous Leydig cells of the human testis as well as in MA-10 tumor and TM3 non-tumor mouse Leydig cell lines. Within the Leydig cell cytoplasm, immunocytochemical results suggested the occurrence of factors known to activate NOS-I such as glutamate and aspartate, as well as molecules involved in the regulation of the NOS-I activity such as calmodulin and Ca2+/calmodulin-dependent protein kinase II. Leydig cells, Sertoli cells, some endothelial cells of the testis, MA-10- and TM3 mouse Leydig cell lines exhibited a relatively strong NADPH-diaphorase enzyme activity as well. Double sequential immunostainings provided evidence that NOS-like immunoreactivity of the testicular Leydig cells is colocalized with testosterone, calmodulin, aspartate, glutamate, and Ca2+/calmodulin-dependent protein kinase II. Sodium nitro-prusside treatment did not result in increased cGMP formation by MA-10- or TM3 mouse Leydig cells, suggesting that NO produced by these cells acts primarily in a paracrine fashion. The NO produced by NOS-I immunoreactive Leydig cells may act as a messenger: 1) between neighbouring NOS-I positive and/or negative Leydig cells as well as to mediate the action of numerous intracellular and extracellular neuroactive substances and growth factors; 2) between Leydig cells and the muscle cells or pericytes of blood vessels to regulate local blood flow and permeability; and 3) between Leydig cells and pertibular myofibroblasts to influence their contraction and the permeability of the lamina propria.

Adult↗

Generation and immunohistological characterization of monoclonal antibodies against rat ovarian antigens.

Hybridoma cell lines were obtained from mouse splenocytes sensitized to granulosa cells and oocytes collected from rat ovaries at the time of gonadotropin stimulation. Each of the Mabs was characterized by its cell type-specific binding reaction using immunofluorescence, avidin-biotin-peroxidase complex, immunogold-silver staining, and some of the Mabs were characterized by electron microscopic immunocytochemistry. Mabs were divided into four classes. On the basis of the immunohistochemical results and a secondary assay, ELISA with conditioned medium containing granulosa cell-secreted proteins (GSPs) we have concluded: (a) The Mabs (Class 1) reacted with GSPs and recognized antigens located on the plasma membrane of granulosa cells. The reaction depends both on the degree of follicular development and on the position of the cells within the follicles. (b) The general pattern of binding of Mab 2E9 (Class 2) was restricted only to the germinal vesicles of oocytes in antral and Graafian follicles. This result indicated a nuclear modification during the progressive phases of oocyte growth. (c) Same antigens recognized by Mabs from Class 3 and 4 were distributed in the cytoplasm of the oocytes and are a constant feature of all growing oocytes displaying a redistribution during meiotic maturation.

Animals↗

Reinvestigation of the transitional epithelium (urothelium) of the human ureter.

The transitional epithelia (urothelia) of the ureters of 30 patients of different ages were studied by means of light and electron microscopical, histochemical and immunocytochemical methods. A great variability of the normal structural appearance of the urothelium was established. Structural features and the uptake of exogenous peroxidase by the surface epithelial cells provided high endocytotic activity. Urothelial cells take up many low and high molecular weight substances from the urine and further metabolize and transport these toward the subepithelial connective tissue. Lymphocytes, macrophages, monocytes, plasma cells and rarely polymorphonuclear leukocytes are distributed intra- and extraepithelially and are involved in the immunological response to agents which enter the intercellular spaces of the epithelium. These cells are also responsible for the elimination of aged and degenerating superficial squamous cells. The present investigation establishes the existence of immunological defence mechanisms in the adult human urothelium. The results obtained suggest that the human ureter contains three functional barriers directed against aggressive components of the urine: the first represented by structures of the superficial squamous cells, the second by the upper cells of the ureteric intermediate layer and the third comprising epithelial and immunological cells involved in immune defence mechanisms.

Adult↗

The Leydig cell of the human testis--a new member of the diffuse neuroendocrine system.

A number of marker substances for neuronal and neuroendocrine cells have been demonstrated in the cytoplasm of the interstitial Leydig cells of human testes using basic immunocytochemical methods and some of their modifications. We were able to reveal immunoreactivity for enzymes involved in the synthesis of the catecholamines dopamine and noradrenaline (tyrosine hydroxylase, aromatic L-amino acid decarboxylase, dopamine-beta-hydroxylase), for the indolamine 5-hydroxytryptamine (serotonin), as well as for a number of well-known neuronal markers such as the neurofilament protein 200, synaptophysin, chromogranin A + B, the neural cell-adhesion molecule (N-CAM), the microtubule-associated protein (MAP-2), and the calcium-binding proteins: S-100, calbindin and parvalbumin. Immunoreactivity for these substances was found in the majority of the interstitial cells although differences in the staining intensity among the individual Leydig cells and among Leydig cells from different patients were observed. At the electron-microscopic level the Leydig cell cytoplasm was seen to contain microtubules, intermediate- and microfilaments as well as clear (40-60 nm) and dense-core (100-300 nm) vesicles, providing a morphological correlate for some of the immunocytochemical results. Although individual marker substances are not absolutely specific for nerve and neuroendocrine cells, the results obtained, together with the already established neuron-specific enolase-, substance P-, methionine-enkephalin- and proopiomelanocortin (POMC)-derived peptide-like immunoreactivity, provide strong evidence for the neuroendocrine (paraneuronal, APUD-like) nature of the Leydig cells of the human testis.

Adult↗

Different epithelia in the distal human male urethra.

The distal segment of the human male urethra, in particular the fossa navicularis, was studied with light- and electron microscopy as well as by means of histochemical and immunocytochemical methods. The fossa navicularis of the urethra contains a circumscribed zone of extremely thick, non-keratinized stratified squamous epithelium composed of cells containing a large amount of glycogen. These cells lack acid phosphatase activity and lysozyme-like immunoreactivity, both of which can be demonstrated to varying extents in the other zones of the distal male urethra. These glycogenrich cells are considered to be the substrate for an endogenous flora of lactobacteria, whereas the acid-phosphatase activity and the lysozyme-like immunoreactivity indicate the presence of macrophages and the secretion of bactericidal agents at the epithelial surface. These observations suggest that the different zones with heterogeneous properties in the distal male urethra probably represent a defense system against the invasion of pathogenic microorganisms. Moreover, the glycogen-rich zone, which resembles the glycogen-rich epithelium of the vagina, is estrogen-dependent. This is demonstrated in cases of sex reversal in which after long-lasting estrogen treatment the glycogen-rich zone becomes extremely extended by displacement of the neighbouring epithelium.

Adolescent↗

Age-related changes in serotonin-immunoreactivity in the telencephalon and diencephalon of rats.

Comparison of the appearance and density of the serotoninergic fibers and terminals in some tel- and diencephalon areas of young adult (3 months) and aged (28 months) rats was made immunohistochemically using an antibody to serotonin. In young adult rats a characteristic arrangement of the serotonin-immunoreactive (SER-IR) fibers and terminals in the tel- and diencephalon was observed. In aged rats the distribution pattern was the same but changes in the appearance and density of the SER-IR fibers were demonstrated. Many swollen and folded fibers forming cluster-like structures as well as reduced fiber networks were seen in the neocortex, hippocampal formation and striatum of aged rats. Aberrant fibers and decreased fiber density were also observed in the bed nucleus of the stria terminalis, lateral septum, nucleus accumbens and thalamic nuclei. Reduced fine granular immunostaining and scattered swollen varicosities were found in some amygdaloid and hypothalamic nuclei of aged rats. These results provide further morphological evidence for changes in the serotoninergic innervation during aging.

Aging↗

Cellular architecture of the lamina propria of human seminiferous tubules.

The lamina propria of human seminiferous tubules is composed of 5 to 7 cellular layers separated by laminae of extracellular connective-tissue components. By means of immunocytochemical methods the different nature of the cellular layers could be defined for the first time. Based on the light-microscopic demonstration of both desmin-like and vimentin-like immuno-reactivity in the inner 3 to 4 layers of the lamina propria, these cells can be identified as myofibroblasts. The outermost one or two cellular layers, on the contrary, only show a vimentin-like immunoreactivity indicating the pure fibroblastic nature of these cells. Therefore, the outermost cellular layers are suggested to be derivatives of the interstitium. In cases of disturbed spermatogenesis, the lamina propria is frequently considerably thickened by an increase in the extracellular matrix components between the cellular layers. Whereas the ultrastructural localization of laminin-, collagen type-IV- and fibronectin-like immunoreactivity remains unaffected in the thickened lamina propria, the desmin-like immunoreactive cells of the inner layers strongly decrease in number and staining intensity. Most probably, the myofibroblasts lose their myoid characteristics to participate in the secretion of increased amounts of extracellular matrix components, which in turn presumably block the mediation of the lamina propria between the interstitium and the germinal epithelium. It is still unclear whether the thickened lamina propria provokes the disturbance of spermatogenesis or vice versa.

Aged↗

Angiotensin II immunoreactivity in the vegetative regions of the thoracic and sacral spinal cord of guinea pig and rat.

The localization of angiotensin-II immunoreactivity (Ang-II-IR) has been studied in the thoracic and sacral spinal cord vegetative regions of male and female guinea pigs and rats. Immunoreactivity is located in varicose nerve fibers and axon terminals throughout the studied areas. We have not observed any immunoreactive neurons in these regions. The highest density of IR structures was observed in the thoracic and sacral vegetative networks of both studied species (Galabov and Davidoff, 1976; Galabov, 1978). Additionally IR fibers and terminals were found between the ependymocytes and in close contact with blood vessels. Slight immunostaining of the apical poles of the ependymocytes was observed too. These localizations of the IR fibers and terminals suggest that Ang II has important functional significance in the regulation of the vegetative activity, and plays some role in the local blood flow regulation. As to the origin of the Ang II-IR fibers and terminals most probably they are coming from higher levels of the central nervous system (brainstem and hypothalamus).

Angiotensin II↗

The vegetative network in the thoracolumbar spinal cord of the guinea pig: a comparison of the distribution of AChE-enzyme activity and choline acetyltransferase-like immunoreactivity.

Histochemically the acetylcholinesterase (AChE) enzyme activity and immunocytochemically the choline acetyltransferase-like immunoreactivity (ChAT-LI) were located in the components of the vegetative network of the thoracolumbar spinal cord of the guinea pig. Both reaction products showed an identical distribution among the preganglionic sympathetic cells and the processes of the vegetative network, namely: cells of the nucleus intermediolateralis pars principalis (ILp), the nucleus intermediolateralis pars funicularis (ILf), the nucleus intercalatus spinalis (IC) and the nucleus intercalatus paraependymalis (ICpe; terminology according to Petras and Cummings 1972). In longitudinal horizontal sections through the intermediate zone of the thoracolumbar spinal cord both AChE-positive- and ChAT-like immunoreactive nerve fibers were organized into two longitudinal lateral fascicles (FLL), two longitudinal medial fascicles (FLM) as well as oblique and transverse bundles that interconnect repeatedly the autonomic cell groups of this zone along the spinal cord and contribute to the ladder-like shape of the vegetative network. The ChAT-like immunostaining of the vegetative network showed that the dendrites of the ILp cells are oriented mainly in a rostrocaudal, but also in a mediolateral direction. Similar orientation of the dendrites was observed for the ICpe cell groups of the thoracolumbar intermediate zone. Thus it is evident that ILp cell bodies and dendrites are involved in the formation of the FLL, whereas the ICpe cells and their dendrites--of the FLM. The IC cells send their dendrites towards both the ILp and ICpe cells and build up together with dendrites of the ILp and ICpe cells the transverse and oblique interconnecting bundles. The vegetative network is strongly developed within the intermediate zone of T1-T4 (mostly T3) and T7-T8 segments of the spinal cord. In these segments a greater variety of interconnections between the preganglionic sympathetic cell groups which are constituents of the network are also revealed. In the remaining segments the vegetative network is more poor developed. In the first two lumbar segments the distance between the interconnecting bundles in the rostrocaudal direction diminishes to 100 microns in contrast to 300-500 microns within the upper segments. The results obtained reveal that the cholinergic preganglionic sympathetic nuclei of the intermediate zone of the thoracolumbar spinal cord together with their dendrites represent the basis (frame) of the ladder-like vegetative network to which join in addition different peptidergic fibers of supraspinal, peripheral and propriospinal origin.

Acetylcholinesterase↗

Coexistence of GABA- and choline acetyltransferase (ChAT)-like immunoreactivity in the hypoglossal nucleus of the rat.

Single and sequential double immunocytochemical techniques were applied to localize gamma-aminobutyric acid (GABA)- and choline acetyltransferase (ChAT)- like immunoreactivity (-LI) in the hypoglossal nucleus of the rat. After subsequential double staining a relatively high number of hypoglossal motor neurons showed the coexistence of both ChAT- and GABA-LI. Coexistence of both substances was also revealed in the axons of the hypoglossal nerve situated within the medulla oblongata. Cells showing only ChAT- or GABA-LI were also observed. Differences in immunostaining between the different cell groups of the hypoglossal nucleus were established. Following axotomy of the right hypoglossal nerve, a decrease or loss of the immunoreactivity for both ChAT and GABA in the motor neurons was established until the 3rd week after the operation. The results obtained do not give evidence on the origin of the GABA-like immunoreactive material and its functional significance in the cholinergic neurons. It can be only speculated that the GABA-like material is either taken up from the intercellular space or is synthesized by the ChAT-LI nerve cells. Functionally, the importance of GABA for the synthesis of gamma-hydroxybutyrate (a novel neurotransmitter candidate) and its postsynaptic transmitter action or presynaptic regulatory action (through autoreceptors in the membrane of the nerve endings) on the release of acetylcholine (ACh) should be taken into consideration.

Acetylcholine↗

Are Leydig cells of neural origin? Substance P-like immunoreactivity in human testicular tissue.

Using the immunocytochemical peroxidase-antiperoxidase method we observed strong and selective staining of Leydig cells after incubation of human testicular tissue with an antiserum against substance P and a slightly weaker immunoreactivity against methionine-enkephalin. These results indicate that the embryologic origin of Leydig cells may require reconsideration and also offer a new perspective for research upon the local control mechanisms of spermatogenesis.

Adult↗

Localization of substance P-like immunoreactive fibers in the thoracic spinal cord of guinea pig.

A dorsal-horn fiber system is revealed in the thoracic spinal cord of guinea pig by means of substance P immunocytochemistry. This system has repeated craniocaudal and/or caudo-cranial extensions and possesses five main components: a superficial network, situated beneath the dorsolateral surface of the spinal cord. This network is connected with the dorsal root fibers and the accumulations of substance P-like immunoreactive (SP-LI) fibers in the Lissauer's tract; an accumulation of SP-LI fibers in the Lissauer's tract at the border of the dorsal horn; two collateral SP-LI fascicles (one lateral and one medial) emerging from the SP-LI fiber accumulation in the Lissauer's tract; a transversal fascicle running through laminae III-V, and an SP-LI network in the region of the lateral spinal cord nucleus. These components of the dorsal-horn fiber system show widespread connections with ipsi- and contralateral spinal cord areas, connecting them in cranio-caudal and/or caudo-cranial directions. The SP-LI dorsal-horn system has close relationship with groups of preganglionic sympathetic cells in the intermediate zone of the spinal cord, respective with the vegetative network of this zone. It is suggested that some fibers of the dorsal-horn system that originate from dorsal-root ganglia may represent primary sensory or visceral afferents. It is likely that the dorsal-horn fiber system and the vegetative network of the thoracic spinal cord may represent the morphological basis for the integration of the central and peripheral vegetative nervous systems, and the somatic and vegetative nervous system.

Animals↗

Acetylcholinesterase activity and type C synapses in the hypoglossal, facial and spinal-cord motor nuclei of rats. An electron-microscope study.

Using the electron-microscope technique of Lewis and Shute, we studied the localization of the acetylcholinesterase (AChE) activity in the hypoglossal, facial and spinal-cord motor nuclei of rats. The technique used selectively detects synapses with subsynaptic cisterns (type C synapses) as well as heavy deposits of reaction products in the rough endoplasmic reticulum, in fragments of the nuclear envelope, in some Golgi zones and on parts of the pericaryal plasma membrane, the axolemma and the dendritic membrane. In C synapses, AChE activity was located in the synaptic cleft and on the membrane of presynaptic boutons. Some C synapses exhibited distinct synaptic specialization in the form of multiple 'active zones'. These zones were characterized by dense presynaptic projections, short dilations of the synaptic cleft, and postsynaptic densities localized between the postsynaptic membrane and the outer membrane of the subsynaptic cistern. Within the postsynaptic densities, rows of rod- or channel-like structures were observed. The subsynaptic cisterns were continuous with the positive rough endoplasmic reticulum. The results are discussed in terms of the possible role of C synapses in the regulation of AChE synthesis in postsynaptic cholinergic neurons and/or in the regulation of AChE release into the extracellular space as well as in the establishment of new synaptic contacts.

Acetylcholinesterase↗

Immunocytochemistry--possibilities for detection of different tissue antigens and establishment of the functional role of cells.

The present review underlines briefly the wide distribution and application of the main immunocytochemical methods for the detection and localization of numerous antigens in tissue sections. For example, a lot of neuroactive substances have been revealed in structures of the central and peripheral nervous system by means of immunocytochemical techniques. The results obtained serve for the better understanding of the main physiological role and the interrelationships of different neuronal classes. Furthermore, some important problems accompanying an immunocytochemical staining connected with the quality of the antibodies used, with the resemblance of the chemical composition of different antigens, and with the coexistence of more neuroactive substances in a nerve cell are pointed out.

Animals↗

Localization of some neuropeptide- and serotonin-like immunoreactivities in the vegetative network of guinea pig spinal cord.

The localization of Substance P(SP)-, Methionine-Enkephalin(met-Enk)-, Somatostatin(SOM)- Serotonin(SER)-, Cholecystokinin(CCK)-, and Vasoactive intestinal polypeptide (VIP)-like immunoreactivity (-LIR) has been determined immunocytochemically in the thoracic spinal cord intermediate zone of male and female guinea pigs. All neuroactive substances studied are exclusively localized in nerve fibre varicosities and terminals building up the vegetative network of the thoracic spinal cord intermediate zone. This network is situated dorsally to the central canal as a longitudinal plate of approximate thickness of 90-100 microns. Immunoreactive fibres are observed in the two Fasciculi longitudinales laterales and the two Fasciculi longitudinales mediales which are interconnected by transverse and oblique peptide-containing bundles (the terminology used by Petras and Cummings 1972; Galabov and Davidoff 1976). All these bundles interconnect the nuclei intermediolaterales principales and funiculares, the nuclei intercalates spinales and the nuclei intercalates paraependimales in ipsi- and contralateral as well as in rostral and caudal direction. The neurones of these nuclei are surrounded by immunoreactive varicosities and terminals. The quantity of the immunoreactive structures and intensity of the staining varied for the different neuroactive substances. As to the origin of the vegetative network immunoreactive fibres three main possibilities exists: a). From primary afferent neurones situated in the dorsal root ganglia, which send their axons via the dorsal roots (mainly for SP and perhaps for CCK); b). From supraspinal neurones which send their axons descending in the white matter funiculi and in the fasciculi longitudinales laterales and mediales and c). From intrinsic spinal cord neurones, which send their neurites in ascending and descending directions, ipsi- and contralaterally and interconnect the spinal cord segments. The different origin of the vegetative network immunoreactive fibres as well as the complex innervation of the preganglionic sympathetic nerve cells in the intermediate zone of the spinal cord suggests that this network may play an important role in the integration of the central and peripheral vegetative nervous system as well as probably in the integration of the somatic and the vegetative nervous system.

Animals↗

Identification and immunocytochemical localization of a human adult brain-specific antigen (HABSA).

A new protein with a molecular weight of 669,000, identified in brain extracts from 4 to 69 years old subjects has been isolated and immunochemically characterized. The antigen is found in human adult brain but not in the brains of human fetuses and newborn infants or in the brains of several other species tested. Immunocytochemically, using the PAP method, the antigen is localized at the surface of some nerve cells and on astrocytes and oligodendrocytes of the cerebral cortex, corpus striatum, pons and medulla. The Golgi epithelial cells with Bergmann's fibers, and the velate and ordinary astrocytes in the cerebellum show immunoreactivity as well.

Adult↗