Pituicytes, glia and control of terminal secretion.

Once thought to be hormone-synthesizing cells, the pituicytes are now known to be the resident astroglia of the neurohypophysis (also referred to here as the posterior pituitary). Early investigators interpreted light microscopic observations as demonstrating pituicyte secretion, since pituicytes appeared to contain neuro-secretory material when hormone demand was low and not when it was increased. Ultrastructural studies have shown that pituicytes actually engulf or completely surround neurosecretory axons and axonal endings under basal conditions, and release these neural processes when conditions require increased hormone output. Thus, the pituicytes appeared to the early workers to contain and release hormone when they actually contained and released axons and terminals in which the hormone was, in fact, contained. Dynamic interactions of pituicytes with various of the other elements in the gland have also been demonstrated. When hormone demand is low, the pituicytes not only engulf the neurosecretory processes but also interpose their own processes between the secretory endings and the basal lamina. Since any hormone that is secreted must pass through the basal lamina and into the perivascular spaces in order to enter the fenestrated capillaries, pituicyte interpositions form physical, and perhaps chemical, barriers to hormone entering the circulation. Increasing hormone demand results in retraction of pituicyte processes from the basal lamina, permitting increased neural contact. Studies of isolated neurohypophysis and of cultured adult rat pituicytes have shown that these glia undergo appropriate morphological changes in response to osmotic stimuli or to receptor-mediated activation of adenylate cyclase. Both these events are thought to be effectors of the alterations seen in vivo. Some possible mechanisms by which pituicytes may participate in the control of secretory events are discussed.

[1]  D. Poulain,et al.  Electrophysiology of hypothalamic magnocellular neurones secreting oxytocin and vasopressin , 1982, Neuroscience.

[2]  J. Nordmann Hormone content and movement of neurosecretory granules in the rat neural lobe during and after dehydration. , 1985, Neuroendocrinology.

[3]  K. H. Backus,et al.  γ-Aminobutyric acid opens Cl-channels in cultured astrocytes , 1987, Brain Research.

[4]  C. P. Leblond,et al.  Increased proliferation of neuroglia and endothelial cells in the supraoptic nucleus and hypophysial neural lobe of young rats drinking hypertonic sodium chloride solution , 1977, The Journal of comparative neurology.

[5]  L. Hösli,et al.  Evidence for the existence of α- and β-adrenoceptors on cultured glial cells—an electrophysiological study , 1982, Neuroscience.

[6]  C. Tweedle,et al.  Evidence for dynamic interactions between pituicytes and neurosecretory axons in the rat , 1980, Neuroscience.

[7]  B. Hamprecht,et al.  Effects of Neurohormones on Glial Cells1 , 1980 .

[8]  Michael R. Hartley,et al.  Autoradiographic localization of peripheral benzodiazepine, dihydroalprenolol and arginine vasopressin binding sites in the pituitaries of control, stalk transected and Brattleboro rats. , 1986, Neuroendocrinology.

[9]  L. Hösli,et al.  Evidence for the existence of alpha- and beta-adrenoceptors on neurones and glial cells of cultured rat central nervous system--an autoradiographic study. , 1982, Neuroscience.

[10]  G. Nilaver,et al.  Immunoreactive glial fibrillary acidic protein in pituicytes of the rat neurohypophysis , 1982, Brain Research.

[11]  F. Leeuwen,et al.  Enkephalin immunoreactivity in synaptoid elements on glial cells in the rat neural lobe , 1983, Neuroscience.

[12]  M. Murray Effects of dehydration on the rate of proliferation of hypothalamic neuroglia cells. , 1968, Experimental neurology.

[13]  W. Mason,et al.  Central release of oxytocin, vasopressin and neurophysin by magnocellular neurone depolarization: evidence in slices of guinea pig and rat hypothalamus. , 1986, Neuroendocrinology.

[14]  D. Sharman,et al.  Effect of water and salt intake on pituitary catecholamines in the rat and domestic pig , 1980, Neuroscience.

[15]  S. W. Ranson,et al.  Diabetes Insipidus and the Neuro-hormonal Control of Water Balance , 1938 .

[16]  L. S. Perlmutter,et al.  Plasticity in the in vitro neurohypophysis: Effects of osmotic changes on pituicytes , 1984, Neuroscience.

[17]  H. Jasper,et al.  Gammaaminobutyric acid. , 1959, Physiological reviews.

[18]  W. Mason,et al.  Axon collaterals of supraoptic neurones: Anatomical and electrophysiological evidence for their existence in the lateral hypothalamus , 1984, Neuroscience.

[19]  M. Geffard,et al.  Ultrastructural localization of GABA in the supraoptic nucleus and neural lobe , 1987, Neuroscience.

[20]  C. Tweedle,et al.  Magnocellular neuropeptidergic terminals in neurohypophysis: Rapid glial release of enclosed axons during parturition , 1982, Brain Research Bulletin.

[21]  J. Morris Organization of neural inputs to the supraoptic and paraventricular nuclei: anatomical aspects. , 1983, Progress in brain research.

[22]  M. Minchin,et al.  The release of [3H]gamma-aminobutyric acid and neurophysin from the isolated rat posterior pituitary , 1975, Brain Research.

[23]  A. Salm,et al.  Extranuclear axon collaterals of paraventricular neurons in the rat hypothalamus: Intracellular staining, immunocytochemistry and electrophysiology , 1985, Brain Research Bulletin.

[24]  L. Renaud Magnocellular neuroendocrine neurons: update on intrinsic properties, synaptic inputs and neurophamacology , 1987, Trends in Neurosciences.

[25]  L. S. Perlmutter,et al.  Neuronal/glial plasticity in the supraoptic dendritic zone in response to acute and chronic dehydration , 1985, Brain Research.

[26]  L. Hösli,et al.  Autoradiographic localization of binding sites for [3H]histamine and H1- and H2-antagonists on cultured neurones and glial cells , 1984, Neuroscience.

[27]  C. Tweedle,et al.  Morphological adaptability at neurosecretory axonal endings on the neurovascular contact zone of the rat neurohypophysis , 1987, Neuroscience.

[28]  L. S. Perlmutter,et al.  Dynamic neuronal-glial interactions in hypothalamus and pituitary: Implications for control of hormone synthesis and release , 1984, Peptides.

[29]  L. Hösli,et al.  Evidence for the existence of alpha- and beta-adrenoceptors on cultured glial cells--an electrophysiological study. , 1982, Neuroscience.

[30]  G. I. Hatton Cellular reorganization in neuroendocrine secretion , 1988 .

[31]  T. Hökfelt,et al.  GABA neuron systems in hypothalamus and the pituitary gland. Immunohistochemical demonstration using antibodies against glutamate decarboxylase. , 1982, Neuroendocrinology.

[32]  V. Pliska,et al.  Identification of the pituicytes as astroglial cells by indirect immunofluorescence-staining for the glial fibrillary acidic protein , 1981, Brain Research.

[33]  L. Hösli,et al.  Evidence for the existence of α- and β-adrenoceptors on neurones and glial cells of cultured rat central nervous system—an autoradiographic study , 1982, Neuroscience.

[34]  E. Scharrer,et al.  The site of origin of the hormones of the posterior pituitary. , 1951, American scientist.

[35]  I. Gersh The structure and function of the parenchymatous glandular cells in the neurohypophysis of the rat , 1939 .

[36]  J. Morris,et al.  Membrane recapture after hormone release from nerve endings in the neural lobe of the rat pituitary gland , 1980, Neuroscience.