The effect of pancreatic mesenchyme on the differentiation of endocrine cells from gastric endoderm

Development ◽  
1987 ◽  
Vol 100 (4) ◽  
pp. 661-671 ◽  
Author(s):  
B. Kramer ◽  
A. Andrew ◽  
B.B. Rawdon ◽  
P. Becker
Keyword(s):  
Endocrine Cell ◽  
Endocrine Cells ◽  
Cell Types ◽  
The Other ◽  
Chick Embryos ◽  
Cell Type ◽  
Pancreatic Insulin ◽  
Somatostatin Cells ◽  
Regional Specificity ◽  
Gut Endocrine Cells

To determine whether mesenchyme plays a part in the differentiation of gut endocrine cells, proventricular endoderm from 4- to 5-day chick or quail embryos was associated with mesenchyme from the dorsal pancreatic bud of chick embryos of the same age. The combinations were grown on the chorioallantoic membranes of host chick embryos until they reached a total incubation age of 21 days. Proventricular or pancreatic endoderm of the appropriate age and species reassociated with its own mesenchyme provided the controls. Morphogenesis in the experimental grafts corresponded closely to that in proventricular controls, i.e. the pancreatic mesenchyme supported the development of proventricular glands from proventricular endoderm. Insulin, glucagon and somatostatin cells and cells with pancreatic polypeptide-like immunoreactivity differentiated in the pancreatic controls. The latter three endocrine cell types, together with neurotensin and bombesin/gastrin-releasing polypeptide (GRP) cells, developed in proventricular controls and experimental grafts. The proportions of the major types common to proventriculus and pancreas (somatostatin and glucagon cells) were in general similar when experimental grafts were compared with proventricular controls but different when experimental and pancreatic control grafts were compared. Hence pancreatic mesenchyme did not materially affect the proportions of these three cell types in experimental grafts, induced no specific pancreatic (insulin) cell type and allowed the differentiation of the characteristic proventricular endocrine cell types, neurotensin and bombesin/GRP cells. However, an important finding was a significant reduction in the proportion of bombesin/GRP cells, attributable in part to a decrease in their number and in part to an increase in the numbers of endocrine cells of the other types. This indicates that mesenchyme may well play a part in determining the regional specificity of populations of gut endocrine cells.

The distribution of endocrine cell progenitors in the gut of chick embryos

Development ◽  
1984 ◽  
Vol 82 (1) ◽  
pp. 131-145
Author(s):  
B. B. Rawdon ◽  
Beverley Kramer ◽  
Ann Andrew
Keyword(s):  
Gastrointestinal Tract ◽  
Progenitor Cells ◽  
Digestive Tract ◽  
Pancreatic Polypeptide ◽  
Endocrine Cell ◽  
Endocrine Cells ◽  
Chick Embryos ◽  
Intact Embryo ◽  
Pancreatic Endocrine Cells ◽  
Gut Endocrine Cells

The aim of this experiment was to find out whether or not, at early stages of development, progenitors of the various types of gut endocrine cells are localized to one or more specific regions of the gastrointestinal tract. Transverse strips of blastoderm two to four somites in length were excised between the levels of somites 5 and 27 in chick embryos at 5- to 24-somite stages and were cultured as chorioallantoic grafts. The distribution of endocrine cells in the grafts revealed confined localization of progenitor cells only in the case of insulinimmunoreactive cells. Theprogenitors of cells with somatostatin-, pancreatic polypeptide-, glucagon-, secretin-, gastrin/CCK-, motilin-, neurotensin- and serotonin-like immunoreactivity were distributed along the length of the presumptive gut at the time of explantation; indeed, in many cases they were more widespread than are their differentiated progeny in normal gut of the same age. This finding indicates that conditions in grafts must differ from those that operate in the intact embryo. Also it may explain the occurrence of ectopic gut or pancreatic endocrine cells in tumours of the digestive tract.

scholarly journals Gene Signature of the Human Pancreatic ε Cell

Endocrinology ◽  
2018 ◽  
Vol 159 (12) ◽  
pp. 4023-4032 ◽  
Author(s):  
Giselle Dominguez Gutierrez ◽  
Jinrang Kim ◽  
Ann-Hwee Lee ◽  
Jenny Tong ◽  
JingJing Niu ◽  
...  
Keyword(s):  
Endocrine Cell ◽  
Metabolic Pathways ◽  
Cell Types ◽  
Gene Signature ◽  
Human Islet ◽  
Cell Type ◽  
Sequencing Technology ◽  
Surface Receptors ◽  
Molecular Features ◽  
Endocrine Cell Type

Abstract The ghrelin-producing ε cell represents the fifth endocrine cell type in human pancreatic islets. The abundance of ε cells in adult pancreas is extremely low, which has hampered the investigation on the molecular pathways regulating the development and the function of this cell type. In this study, we explored the molecular features defining the function of pancreatic ε cells isolated from adult nondiabetic donors using single-cell RNA sequencing technology. We focus on transcription factors, cell surface receptors, and genes involved in metabolic pathways that contribute to regulation of cellular function. Furthermore, the genes that separate ε cells from the other islet endocrine cell types are presented. This study expands prior knowledge about the genes important for ε cell functioning during development and provides a resource to interrogate the transcriptome of this rare human islet cell type.

The Cytology of the Digestive and Salivary Glands of the Limpet, Patella

1963 ◽  
Vol s3-104 (65) ◽  
pp. 23-37
Author(s):  
D. PUGH
Keyword(s):  
Salivary Gland ◽  
Single Cell ◽  
Salivary Glands ◽  
Cell Types ◽  
The Other ◽  
Cell Type ◽  
Food Material ◽  
Tubular Gland ◽  
Single Cell Type ◽  
Reserve Food

As reported by earlier investigators, the epithelium of the digestive tubules is composed of two cell-types. One type of cell is glandular, the other type is absorptive and digestive, and to a lesser extent secretory. The latter type of cell also contains glycogen and numerous lipid globules, so that the digestive gland as a whole contains a large quantity of reserve food material. The epithelium of the digestive duct possesses a single cell-type; the cells are ciliated and heavily pigmented, and they produce a viscous secretion. The salivary gland is a compound tubular gland. The cells elaborate a secretion containing protein and probably some carbohydrate.

Histomorphological and Cytochemical Characters of Endocrine Cells of the Gastrointestinal Mucosa of Duck (Anas platyrhynchos)

2021 ◽  
Author(s):  
R. Patra ◽  
U.K. Mishra ◽  
S. Palai ◽  
P.R. Sahoo ◽  
S. Mohapatra
Keyword(s):  
Endocrine Cells ◽  
Cell Signalling ◽  
Cell Types ◽  
Enteric Neurons ◽  
Surface Epithelium ◽  
Oval Cell ◽  
Cell Proliferation And Differentiation ◽  
Neck Part ◽  
Gut Endocrine Cells ◽  
Small Clusters

Background: It is known that balance diet is the key success for better production in poultry. The digestive physiology is regulated by the neurocrine and endocrine secretions. Growth, secretion, motility, cell signalling, vasoregulation, cell proliferation and differentiation of the epithelial cells of the alimentary canal are reported to be controlled by the peptides or amines released from the gut endocrine cells and enteric neurons. References particularly on systematic study of gastrointestinal endocrine cells in duck as regards to histomorphology and cytochemistry are gravely scanty. Hence the present investigation envisages authenticating the histomorphological characters and cytochemical behaviour of the gastrointestinal endocrine cells in duck.Methods: For this study the abdomen of six Khaki campbell ducks from either sex was cut open following euthanasia. Tissue pieces from different segments of gut were collected and processed routinely to get 7-8µ thick serial paraffin sections. The tissue sections were stained for evaluation of histomorphological and histochemical characters of the entero-endocrine cells.Result: A panel of seven cytochemical stains identified nine endocrine cell types in the digestive mucosa of Khaki Campbell duck i.e. basally granulated oval cell, densely granulated spindle shaped cell, densely granulated oval cell, diffusely granulated oval cell, pyramidal cell, densely granulated elongated cell, densely granulated pyriform cell, peripherally granulated spherical cell and non-argentaffin chromaffin oval cell. The cells occurred in single or in small clusters in the basal or middle or neck part of glandular epithelium or in the surface epithelium. All the endocrine cells were ‘close type’. Cytochemically they were four types i.e. argentaffin, argyrophil, chromaffin and APUD (Amine precursor uptake and decarboxylation) cells.

Contractile properties of cultured glomerular mesangial cells

1985 ◽  
Vol 249 (4) ◽  
pp. F457-F463 ◽  
Author(s):  
J. I. Kreisberg ◽  
M. Venkatachalam ◽  
D. Troyer
Keyword(s):  
Mesangial Cell ◽  
Mesangial Cells ◽  
Matrix Material ◽  
Cell Types ◽  
Contractile Properties ◽  
The Other ◽  
Glomerular Mesangial Cells ◽  
Cell Type ◽  
Isotonic Contraction ◽  
Prolonged Culture

The glomerular mesangium is composed of matrix material and at least two cell types. One is a bone marrow-derived phagocyte and the other is a smooth muscle-like cell. The phagocytic cell represents approximately 3-7% of the total mesangial cell population. The other, more abundant, cell type appears to be contractile and therefore has been proposed to play a role in regulating the surface area for filtration, one component of the ultrafiltration coefficient, Kf. In this review we discuss the contractile properties of cultured mesangial cells as well as the phenotypic alterations that lead to loss of isotonic contraction after prolonged culture.

scholarly journals Heterogeneity of chromogranin A-derived peptides in bovine gut, pancreas and adrenal medulla

1991 ◽  
Vol 276 (2) ◽  
pp. 471-479 ◽  
Author(s):  
A Watkinson ◽  
A C Jönsson ◽  
M Davison ◽  
J Young ◽  
C M Lee ◽  
...  
Keyword(s):  
Endocrine Cell ◽  
Cell Biology ◽  
Chromogranin A ◽  
Endocrine Cells ◽  
Cell Types ◽  
Intact Protein ◽  
Pancreatic Endocrine Cells ◽  
Gastric Corpus ◽  
Adrenal Chromaffin ◽  
Bovine Pancreas

Chromogranin A is produced in many endocrine cell types, and is widely used as a marker in endocrine-cell pathology and secretory-cell biology. There is some evidence that it may be proteolytically processed to yield the putative pancreatic regulatory peptide, pancreastatin, and, in order to characterize the relevant pathways in gastrointestinal and pancreatic endocrine cells, we have used, in radioimmunoassay, site-directed antibodies to pancreastatin itself (L331) and to a sequence of chromogranin A immediately C-terminal to pancreastatin (L300). The latter antibody revealed three major forms of immunoreactivity of 8 kDa and five peptides of approx. 3 kDa in bovine pancreas and gut extracts. The 8 kDa peptides were characterized as chromogranin A-(248-313)-peptides, i.e. C-terminally extended forms of pancreastatin; two of the 8 kDa variants differed in two positions, confirming a polymorphism predicted from cDNA sequencing. One of the 3 kDa peptides was characterized as chromogranin A-(297-313)-peptide, i.e. the C-terminal heptadecapeptide of the 8 kDa peptide that would be liberated after cleavage to yield pancreastatin. On the basis of chromatographic studies, immunohistochemistry and the stoichiometry of different immunoreactive peptides, three different pathways of chromogranin A processing were identified: in adrenal chromaffin cells chromogranin A existed mainly as the unmodified intact protein, in pancreatic islet and gastric antral endocrine cells pancreastatin and the 3 kDa peptides were major products, but in small intestine and gastric corpus endocrine cells there was little nor no pancreastatin and the 8 kDa cleavage product predominated. There are therefore important differences in the distribution of chromogranin A-derived peptides between quite closely related populations of endocrine cells that are attributable not only to variable post-translational cleavage but also to the expression of different primary sequences. It seems possible that in different cell types chromogranin A-derived peptides might subserve a variety of different functions.

MORPHOLOGY OF ENDOCRINE CELLS IN THE ISLET TISSUE OF THE COD GADUS CALLARIAS

1970 ◽  
Vol 63 (4) ◽  
pp. 679-695 ◽  
Author(s):  
N. W. Thomas
Keyword(s):  
Endocrine Cells ◽  
Secretory Granules ◽  
Cell Types ◽  
Differential Staining ◽  
Cell Type ◽  
Central Mass ◽  
Islet Tissue ◽  
History Of ◽  
Alpha Beta ◽  
Delta Cells

ABSTRACT The principal islet of the cod consists of a central mass of endocrine tissue, surrounded by a capsule of exocrine tissue. Four cell types are recognisable by differential staining and electron microscopy. Three of these correspond in staining reactions and general morphology to alpha, beta and delta cells of other species. Each cell-type contains characteristic secretory granules. The fourth cell-type does not appear to correspond to any other pancreatic endocrine cell although its granules show features common to both alpha and beta cells. It may represent a phase in the life history of one of these cell types or more probably a separate cell-type.

scholarly journals Co-localization of neuroendocrine hormones in the human fetal pancreas

1999 ◽  
pp. 526-533 ◽  
Author(s):  
GM Portela-Gomes ◽  
H Johansson ◽  
L Olding ◽  
L Grimelius
Keyword(s):  
Endocrine Pancreas ◽  
Islet Amyloid Polypeptide ◽  
Gastric Inhibitory Polypeptide ◽  
Cell Types ◽  
Human Fetuses ◽  
Pancreatic Hormones ◽  
Cell Type ◽  
Islet Amyloid ◽  
Fetal Pancreas ◽  
Somatostatin Cells

OBJECTIVE AND DESIGN: Co-localization of the four major pancreatic hormones, and also of islet amyloid polypeptide (IAPP), peptide tyrosine tyrosine (PYY), secretin and neurotensin, has been studied in the endocrine pancreas of human fetuses at 16, 18 and 22 weeks of gestation. METHODS: Double and triple immunofluorescence stainings have been used. RESULTS: All three fetal pancreata contained cells that showed insulin, glucagon, somatostatin, pancreatic polypeptide (PP), IAPP, secretin and PYY immunoreactivity. Neurotensin cells were found in the youngest fetus and gastric inhibitory polypeptide (GIP) in the two older fetuses. Co-localization of two hormones occurred in most of the endocrine cell types in the three fetuses examined, but three hormones occurred in only a few cells and especially in the youngest fetus. Somatostatin cells were the only cell type which was largely monohormonal. Our findings showed that there are two different co-localization patterns: insulin was co-localized mainly with IAPP and glucagon, while secretin and PYY occurred together with glucagon and PP. CONCLUSIONS: These data are the first to describe secretin and neurotensin in the fetal pancreas. Two different co-localization patterns could be distinguished: insulin, IAPP and glucagon, and glucagon, secretin, PP and PYY.

scholarly journals SpatialDWLS: accurate deconvolution of spatial transcriptomic data

2021 ◽  
Author(s):  
Rui Dong ◽  
Guo-Cheng Yuan
Keyword(s):  
Spatial Information ◽  
Cell Types ◽  
Computational Method ◽  
The Other ◽  
Cellular Heterogeneity ◽  
Biological Information ◽  
Cell Type ◽  
Transcriptomic Data ◽  
Cell Type Composition ◽  
Type Composition

AbstractRecent development of spatial transcriptomic technologies has made it possible to systematically characterize cellular heterogeneity while preserving spatial information, which greatly enables the investigation of structural organization of a tissue and its impact on modulating cellular behavior. On the other hand, the technology often does not have sufficient resolution to distinguish neighboring cells which may belong to different cell types, therefore it is difficult to identify cell-type distribution directly from the data. To overcome this challenge, we have developed a computational method, called spatialDWLS, to quantitatively estimate the cell-type composition at each spatial location. We benchmarked the performance of spatialDWLS by comparing with a number of existing deconvolution methods using both real and simulated datasets, and we found that spatialDWLS outperformed the other methods in terms of accuracy and speed. By applying spatialDWLS to analyze a human developmental heart dataset, we observed striking spatial-temporal changes of cell-type composition which becomes increasing spatially coherent during development. As such, spatialDWLS provides a valuable computational tool for faithfully extracting biological information from spatial transcriptomic data.

scholarly journals Postnatal development of intestinal endocrine cell populations in the water buffalo

1999 ◽  
Vol 195 (3) ◽  
pp. 439-446
Author(s):  
CARLA LUCINI ◽  
PAOLO DE GIROLAMO ◽  
LUIGI COPPOLA ◽  
GIUSEPPE PAINO ◽  
LUCIANA CASTALDO
Keyword(s):  
Postnatal Development ◽  
Endocrine Cell ◽  
Endocrine Cells ◽  
Water Buffalo ◽  
Regional Distribution ◽  
Gastric Inhibitory Polypeptide ◽  
Cell Types ◽  
Proximal Colon ◽  
Cell Populations ◽  
Adult Diet

The frequency and distribution of 11 endocrine cell populations were studied in the intestine of differently aged buffalo, grouped on the basis of diet: 2-d-olds (suckling), 5-mo-olds (weaning) and 5-y-olds (ruminant adult diet). The endocrine cell populations were identified immunocytochemically using antisera against 5-hydroxytryptamine (5-HT), somatostatin, gastrin, cholecystokinin (CCK), COOH-terminal octapeptide of gastrin/CCK, neurotensin, motilin, gastric inhibitory polypeptide (GIP), secretin, glucagon/glicentin (GLU/GLI) and polypeptide YY (PYY). In adult buffalos the regional distribution of endocrine cells is similar to that of other adult ruminants. During postnatal development, these cell types showed the following changes in their frequency and distribution: (1) 5-HT, neurotensin and gastrin/CCK immunoreactive cells (i.c.) showed a decrease in frequency with age; (2) somatostatin i.c. frequency remained stable with age; (3) motilin, GIP, secretin and CCK i.c. showed a slight increase in frequency with age; (4) GLU/GLI and PYY i.c. decreased in frequency with age in the small intestine, caecum and proximal colon and an increase in frequency in the rectum. It was hypothesised that the endocrine cell types, whose presence and localisation is substantially stable in all examined ages, probably contain substances that are strictly necessary for intestinal function. In contrast the hormones contained in the cell populations that decreased with age, are probably involved in physiological needs during the milk and weaning diet or play a role in intestinal growth.

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