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Paracrine secretion

A synopsis of the most important data concerning H3 receptors and gastric acid secretion is reported in Tables 1 and 2. Table 3 reports the effects of H3 ligands on hormonal or paracrine secretions which are directly or indirectly connected with acid secretion. [Pg.61]

Fig. 4. Four routes of cellular secretion of gastrin. Several other regulatory systems, wherein the same peptide acts as hormone, neurotransmitter, and growth factor, are also released as they occur in these four cell types. Autocrine and paracrine secretion are assumed to play decisive roles for the growth of malignantly transformed cells. Fig. 4. Four routes of cellular secretion of gastrin. Several other regulatory systems, wherein the same peptide acts as hormone, neurotransmitter, and growth factor, are also released as they occur in these four cell types. Autocrine and paracrine secretion are assumed to play decisive roles for the growth of malignantly transformed cells.
Larsson H, Golterman N, De Magistris L, et al. Somatostatin cell processes as pathways for paracrine secretion. Science 1979 205 1393. Lewin MJM. The somatostatin receptor in the Gl tract. Ann Rev Physiol 1992 54 455. [Pg.127]

Support cells play important roles in regulating the self-renewal, mobilization and differentiation of stem cells. Support cells can interact with stan cells by direct contact through receptors and gap junctions, and by paracrine secretion of growth factors to influence cell fate and functions. In adult tissues, such as the adult brain, it has been shown that the adult hippocampal NSC proliferation occurs in a vascular niche where there is endothelial component of the vasculature, while NSC differentiation is promoted by contact with astrocytes [139]. The concept of support cells is perhaps best represented in vitro by the use of feeder cells [140] and feeder cell-derived matrices [141, 142] to support the self-renewal and pluripotency of hESCs. [Pg.200]

Nontraditional Hormones. Novel hormones identified ia cardiovascular tissue have profound effects on maintenance of blood pressure and blood volume ia mammals. Atrial natriuretic hormone (ANH) is a polypeptide hormone secreted from the atria of the heart. When the cardiac atrium is stretched by increased blood volume, secretion of ANH is stimulated ANH ia turn increases salt and water excretion and reduces blood pressure (6). Endothelin is a polypeptide hormone secreted by endothehal cells throughout the vasculature. Although endothelin is released into the circulation, it acts locally in a paracrine fashion to constrict adjacent vascular smooth muscle and increase blood pressure (7). [Pg.172]

P and Pg, exist in foUicular fluid. Control of inhibin secretion involves a feedback relationship in which circulating FSH stimulates inhibin secretion, which in turn reduces the secretion of FSH (8). Both the homo- and the heterodimers of the P-subunits of inhibin promote the secretion of FSH and thus have been termed activins. Activin is secreted by the ovary and the testes into the circulation. In addition, both inhibin and activin have intragonadal autocrine and paracrine effects that influence gonadal steroidogenesis (9). [Pg.172]

Somatostatin acts on various organs, tissues and cells as neurotransmitter, paracrine/autocrine and endocrine regulator on cell secretion, smooth muscle contractility, nutrient absorption, cell growth and neurotransmission [1]. Some of its mainly inhibitory effects are listed in Table 1. Somatostatin mediates its function via a family of heptahelical G-protein-coupled receptors termed... [Pg.1148]

In addition, several other organs, like the heart, ovaty, amnion, chorion, decidua, testis, epididymis and prostate, have been reported to synthesize OT, suggesting a paracrine role for this hormone in these tissues. Ectopic AVP production by lung cancer cells or other neoplasms has been described in humans, leading to the syndrome of inappropriate antidiuretic hormone secretion. [Pg.1274]

Figure 1. Autocrine and paracrine factors. Many animal cells secrete regulatory factors called autocrine factors, which then interact with specific receptors on the surface of the same cells, so as to modulate cell function. Animal cells may also secrete regulatory factors called paracrine factors, which interact with specific receptors on different cells in the same locale, modulating their functional properties. Figure 1. Autocrine and paracrine factors. Many animal cells secrete regulatory factors called autocrine factors, which then interact with specific receptors on the surface of the same cells, so as to modulate cell function. Animal cells may also secrete regulatory factors called paracrine factors, which interact with specific receptors on different cells in the same locale, modulating their functional properties.
TGFs are secreted by animal cells following their biosynthesis. Subsequently, these TGFs may either stimulate the growth of the very cells that have produced them (in this case, the TGFs act as autocrine factors), or may stimulate the growth of other adjacent cell types (in this case, the TGFs act as paracrine factors). [Pg.481]

The factors are secreted into the extracellular milieu where they diffuse and then act in a paracrine fashion on other cells (Fig. 27-1). Indeed, there is evidence that this type of paracrine support is necessary to sustain neurons as they extend their processes over long distances in the developing nervous system [2]. An analogous process, autocrine stimulation, occurs when a cell synthesizes and secretes a growth factor to which the cell itself is responsive. In this case, the cell provides its own trophic support. [Pg.472]

The receptor for NGF is TrkA, a 140 kDa cell surface protein that specifically binds NGF, but not other neurotrophins [5, 6, 9]. TrkA is expressed on the neuronal cell body and on neuronal processes. In its action as a target-derived trophic factor, NGF is secreted within the target organ and it then binds to TrkA receptors present on the growing neuronal process or synapse. The NGF-TrkA complex is then internalized and subsequently translocated to the cell body by retrograde axonal transport. In those cells that respond to NGF through autocrine or paracrine mechanisms, the growth factor can bind to any of the widely distributed TrkA molecules on the neuronal membrane. [Pg.475]

Adipocytes have an important secretory function. Numerous factors (collectively termed adipokines or adipocytokines), mostly peptides but also eicosanoids are produced by preadipocytes and mature adipocytes (Table 9.3). Some of these factors act in an autocrine or paracrine fashion to regulate adipogenesis, that is differentiation and maturation of adipocytes themselves, whilst others, notably, leptin, adiponectin and some cytokines act in truly endocrine way, having effects on the brain, endothelial cells, liver and skeletal muscle. Disturbance in secretion from adipocytes is associated with eating disorders and metabolic syndrome. [Pg.305]

The GI system is responsible at its most basic level for providing a continual supply of water, electrolytes, minerals, and nutrients. This is achieved by a myriad of specialized cells and coordinated interplay of motility, secretion, digestion, absorption, blood flow, and lymph flow. These components are under elaborate control of the central and enteric nervous systems, endocrine and paracrine regulation of hormones. The highly complex nature of GI function is clearly illustrated by the estimate that 80 to 100 million neurons exist within the enteric nervous system, a number comparable to that found within the spinal column, hence described as a "second brain."171... [Pg.264]


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