Localization of organ-specific antigens in the nervous system of the rat

1977 ◽  
Vol 39 (2) ◽  
pp. 109-114 ◽  
Author(s):  
Halina Weinrauder ◽  
Boles?aw Lach
Development ◽  
1984 ◽  
Vol 80 (1) ◽  
pp. 137-153
Author(s):  
Sadao Yasugi

Quail allantoic endoderm was implanted into the presumptive digestive-tract area of chick embryos, and the differentiation of the endoderm was examined morphologically and immunocytochemically with antisera against pepsinogens and sucrase. The allantoic endoderm was incorporated into the host digestive organs. It often became continuous with the host endoderm and formed a chimaeric digestive-tract epithelium. It differentiated morphologically into the epithelium of the digestive organ into which it was incorporated, showing the morphological inductive ability in situ of the digestive-tract mesenchyme against the allantoic endoderm. However, the allantoic endoderm did not produce pepsinogens even when it was incorporated into the host proventricular mesenchyme and formed well-developed proventricular glands. This result indicates that the heterotypic morphogenesis of the allantoic endoderm is not necessarily accompanied by the heterotypic cytodifferentiation. In contrast, the anti-sucrase antiserum-reactive cells often differentiated in the allantoic endoderm incorporated into not only the intestine but also other organs. This confirmed our previous observation that the allantoic endoderm has a tendency to differentiate into the intestinal epithelium in the heterologous environment.


2010 ◽  
Vol 108 (2) ◽  
pp. 227-237 ◽  
Author(s):  
Murray Esler

Sympathetic nervous system responses typically are regionally differentiated, with activation in one outflow sometimes accompanying no change or sympathetic inhibition in another. Regional sympathetic activity is best studied in humans by recording from postganglionic sympathetic efferents (multiunit or single fiber recording) and by isotope dilution-derived measurement of organ-specific norepinephrine release to plasma (regional “norepinephrine spillover”). Evidence assembled in this review indicates that sympathetic nervous system abnormalities are crucial in the development of cardiovascular disorders, notably heart failure, essential hypertension, disorders of postural circulatory control causing syncope, and “psychogenic heart disease,” heart disease attributable to mental stress and psychiatric illness. These abnormalities involve persistent, adverse activation of sympathetic outflows to the heart and kidneys in heart failure and hypertension, episodic or ongoing cardiac sympathetic activation in psychogenic heart disease, and defective sympathetic circulatory reflexes in disorders of postural circulatory control. An important goal for clinical scientists is translation of knowledge of pathophysiology, such as this, into better treatment for patients. The achievement of this “mechanisms-to-management” transition is at differing stages of development with the different conditions. Clinical translation is mature in cardiac failure, knowledge of cardiac neural pathophysiology having led to introduction of β-adrenergic blockers, an effective therapy. With essential hypertension, perhaps we are on the cusp of effective translation, with recent successful testing of selective catheter-based renal sympathetic nerve ablation in patients with resistant hypertension, an intervention firmly based on demonstration of activation of the renal sympathetic outflow. With psychogenic heart disease and postural syncope syndromes, knowledge of the neural pathophysiology is emerging, but clinical translation remains for the future.


Author(s):  
Günther Loose ◽  
Günter Vogt ◽  
Mireille Charmantier-Daures ◽  
Guy Charmantier ◽  
Steffen Harzsch

This chapter reviews the development of the major organ systems in crustaceans, including musculature, nervous system, circulatory system, digestive system, osmoregulatory system, excretory system, reproductive system, and sensory organs. It describes the morphological unfolding of these organ systems, which generally follows cleavage, gastrulation, and segmentation in the course of ontogeny. Particular emphasis is given to the organ-specific temporal dynamics of development, the onset of functionality, and possible correlations with developmental mode, life history, and ecology. The anatomy and cellular characteristics of developing organs are generally better investigated than aspects of physiology, biochemistry, and molecular biology. Investigations in different crustaceans revealed that the speed of development of the various organ systems varies considerably within an individual and between species. As a rule of thumb, anlagen of the nervous tissue, muscular tissue, digestive system, and excretory organs appear first, followed by the circulatory system. Osmoregulatory organs are formed later. The reproductive organs are the last to emerge and to become functional. The mode of development, behavior, and ecology of the postembryonic stages seem to be major determinants that influence the speed differences of organogenesis. This is reflected by timing differences in development of the digestive system between directly and indirectly developing representatives or species with or without lecithotrophic larvae. Other features of the dynamics of organogenesis suggest evolutionary constraints, such as the delayed development of the nervous system in postnaupliar, relative to naupliar, segments in some species. Mechanistic constraints may be involved in heart development and development of nontransitory osmoregulatory organs.


2010 ◽  
Vol 207 (9) ◽  
pp. 1907-1921 ◽  
Author(s):  
Junwei Hao ◽  
Ruolan Liu ◽  
Wenhua Piao ◽  
Qinghua Zhou ◽  
Timothy L. Vollmer ◽  
...  

Natural killer (NK) cells of the innate immune system can profoundly impact the development of adaptive immune responses. Inflammatory and autoimmune responses in anatomical locations such as the central nervous system (CNS) differ substantially from those found in peripheral organs. We show in a mouse model of multiple sclerosis that NK cell enrichment results in disease amelioration, whereas selective blockade of NK cell homing to the CNS results in disease exacerbation. Importantly, the effects of NK cells on CNS pathology were dependent on the activity of CNS-resident, but not peripheral, NK cells. This activity of CNS-resident NK cells involved interactions with microglia and suppression of myelin-reactive Th17 cells. Our studies suggest an organ-specific activity of NK cells on the magnitude of CNS inflammation, providing potential new targets for therapeutic intervention.


1963 ◽  
Vol 54 (3) ◽  
pp. 1010-1013
Author(s):  
A. T. Kravchenko ◽  
N. A. Kolesnikova ◽  
G. T. Patrikeev

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