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.

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.

scholarly journals The SNAG Domain of Insm1 Regulates Pancreatic Endocrine Cell Differentiation and Represses Beta- to Delta-Cell Transdifferentiation

2021 ◽  
Author(s):  
Xuehua Liang ◽  
Hualin Duan ◽  
Yahui Mao ◽  
Ulrich Koestner ◽  
Yiqiu Wei ◽  
...  
Keyword(s):  
Cell Differentiation ◽  
Beta Cell ◽  
Endocrine Cell ◽  
Endocrine Cells ◽  
Cell Number ◽  
Pancreatic Endocrine Cell ◽  
Cell Transdifferentiation ◽  
Pancreatic Endocrine Cells ◽  
Delta Cell ◽  
Null Mutants

The allocation and specification of pancreatic endocrine lineages are tightly regulated by transcription factors. Disturbances in differentiation of these lineages contribute to the development of various metabolic diseases, including diabetes. The Insulinoma-associated protein 1 (<i>Insm1</i>), which encodes a protein containing one SNAG domain and five zinc fingers, plays essential roles in pancreatic endocrine cell differentiation and in mature beta-cell function. In the present study, we compared the differentiation of pancreatic endocrine cells between Insm1 null and Insm1 SNAG domain mutants (Insm1delSNAG) to explore the specific function of the SNAG domain of Insm1. We show that the delta-cell number is increased in Insm1delSNAG but not in Insm1 null mutants as compared to the control mice. We also show a less severe reduction of the beta-cell number in Insm1delSNAG as that in Insm1 null mutants. In addition, similar deficits are observed in alpha-, PP- and epsilon-cell in Insm1delSNAG and Insm1 null mutants. We further identified that the increased delta-cell number is due to beta- to delta-cell transdifferentiation. Mechanistically, the SNAG domain of Insm1 interacts with Lsd1, the demethylase of H3K4me1/2. Mutation in the SNAG domain of Insm1 results in impaired recruitment of Lsd1 and increased H3K4me1/2 levels at <i>H</i><i>hex</i> loci that are bound by Insm1, thereby promoting the transcriptional activity of the delta-cell-specific gene <i>Hhex</i>. Our study has identified a novel function of the SNAG domain of Insm1 in the regulation of pancreatic endocrine cells differentiation, particularly in the repression of beta- to delta-cell transdifferentiation.

scholarly journals Immunocytochemical study of the distribuition of endocrine cells in the pancreas of the Brazilian sparrow species Zonotrichia Capensis Subtorquata (Swaison, 1837)

2007 ◽  
Vol 67 (4) ◽  
pp. 735-740 ◽  
Author(s):  
AA Nascimento ◽  
A Sales ◽  
TRD Cardoso ◽  
NL Pinheiro ◽  
RMM Mendes
Keyword(s):  
B Cells ◽  
Pancreatic Islets ◽  
Pancreatic Polypeptide ◽  
Endocrine Cells ◽  
Central Place ◽  
Immunocytochemical Study ◽  
Zonotrichia Capensis ◽  
Specific Antisera ◽  
Pancreatic Endocrine Cells ◽  
Avian Pancreatic Polypeptide

In the present study, we investigated types of pancreatic endocrine cells and its respective peptides in the Brazilian sparrow species using immunocytochemistry. The use of polyclonal specific antisera for somatostatin, glucagon, avian pancreatic polypeptide (APP), YY polypeptide (PYY) and insulin, revealed a diversified distribution in the pancreas. All these types of immunoreactive cells were observed in the pancreas with different amounts. Insulin- Immunoreactive cells to (B cells) were most numerous, preferably occupying the central place in the pancreatic islets. Somatostatin, PPA, PYY and glucagon immunoreactive cells occurred in a lower frequency in the periphery of pancreatic islets.

scholarly journals Localization of amidating enzymes (PAM) in rat gastrointestinal tract.

1993 ◽  
Vol 41 (11) ◽  
pp. 1617-1622 ◽  
Author(s):  
A Martínez ◽  
M A Burrell ◽  
M Kuijk ◽  
L M Montuenga ◽  
A Treston ◽  
...  
Keyword(s):  
Small Intestine ◽  
In Situ Hybridization ◽  
Gastrointestinal Tract ◽  
Digestive Tract ◽  
Endocrine Cells ◽  
Regulatory Peptides ◽  
Serial Sections ◽  
Gastric Glands ◽  
Amidating Enzymes

We studied the distribution of the two enzymes involved in post-translational C-terminal alpha-amidation of regulatory peptides in rat digestive tract, using immunocytochemical methods and in situ hybridization techniques. The enzymes were located in most of the fibers and neurons of the myenteric and submucous plexus throughout the entire digestive tract and in endocrine cells of the stomach and colon. Staining of reverse-face serial sections demonstrated that the enzymes in endocrine cells of the stomach co-localized with gastrin in the bottom of the gastric glands. Some gastrin-immunoreactive cells near the neck of the gland were negative for PAM, suggesting that amidation takes place only in the more mature cells. In the colon all cells immunoreactive for glucagon and GLP1 were also positive for peptidylglycine alpha-hydroxylating monooxygenase (PHM) but not for peptidyl-alpha-hydroxyglycine alpha-amidating lyase (PAL). The absence of immunoreactivity for the amidating enzymes in endocrine cells of the small intestine, known to produce C-terminally amidated peptides, suggests the existence of other amidating enzymes.

Coexistence of pancreatic polypeptide (PP)-and glucagon-immunoreactivity in pancreatic endocrine cells of mouse

1987 ◽  
Vol 87 (1) ◽  
pp. 1-6 ◽  
Author(s):  
J. H. W. M. Rombout ◽  
M. E. Abad ◽  
F. M. Peeze Binkhorst ◽  
J. J. Taverne-Thiele
Keyword(s):  
Pancreatic Polypeptide ◽  
Endocrine Cells ◽  
Pancreatic Endocrine Cells ◽  
Glucagon Immunoreactivity

scholarly journals The SNAG Domain of Insm1 Regulates Pancreatic Endocrine Cell Differentiation and Represses Beta- to Delta-Cell Transdifferentiation

2021 ◽  
Author(s):  
Xuehua Liang ◽  
Hualin Duan ◽  
Yahui Mao ◽  
Ulrich Koestner ◽  
Yiqiu Wei ◽  
...  
Keyword(s):  
Cell Differentiation ◽  
Beta Cell ◽  
Endocrine Cell ◽  
Endocrine Cells ◽  
Cell Number ◽  
Pancreatic Endocrine Cell ◽  
Cell Transdifferentiation ◽  
Pancreatic Endocrine Cells ◽  
Delta Cell ◽  
Null Mutants

The allocation and specification of pancreatic endocrine lineages are tightly regulated by transcription factors. Disturbances in differentiation of these lineages contribute to the development of various metabolic diseases, including diabetes. The Insulinoma-associated protein 1 (<i>Insm1</i>), which encodes a protein containing one SNAG domain and five zinc fingers, plays essential roles in pancreatic endocrine cell differentiation and in mature beta-cell function. In the present study, we compared the differentiation of pancreatic endocrine cells between Insm1 null and Insm1 SNAG domain mutants (Insm1delSNAG) to explore the specific function of the SNAG domain of Insm1. We show that the delta-cell number is increased in Insm1delSNAG but not in Insm1 null mutants as compared to the control mice. We also show a less severe reduction of the beta-cell number in Insm1delSNAG as that in Insm1 null mutants. In addition, similar deficits are observed in alpha-, PP- and epsilon-cell in Insm1delSNAG and Insm1 null mutants. We further identified that the increased delta-cell number is due to beta- to delta-cell transdifferentiation. Mechanistically, the SNAG domain of Insm1 interacts with Lsd1, the demethylase of H3K4me1/2. Mutation in the SNAG domain of Insm1 results in impaired recruitment of Lsd1 and increased H3K4me1/2 levels at <i>H</i><i>hex</i> loci that are bound by Insm1, thereby promoting the transcriptional activity of the delta-cell-specific gene <i>Hhex</i>. Our study has identified a novel function of the SNAG domain of Insm1 in the regulation of pancreatic endocrine cells differentiation, particularly in the repression of beta- to delta-cell transdifferentiation.

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.

An immunocytochemical study of regulatory peptides in the amphibian gastrointestinal tract

1986 ◽  
Vol 64 (1) ◽  
pp. 1-7 ◽  
Author(s):  
A. M. J. Buchan
Keyword(s):  
Gastrointestinal Tract ◽  
Substance P ◽  
Vasoactive Intestinal Polypeptide ◽  
Pancreatic Polypeptide ◽  
Endocrine Cells ◽  
Regulatory Peptides ◽  
Single Species ◽  
Gastric Inhibitory Polypeptide ◽  
Ambystoma Mexicanum ◽  
Intestinal Polypeptide

Samples from the gastrointestinal tract of two urodele and eight anuran species were investigated by immunocytochemical methods for the presence of structures immunoreactive with a range of antisera raised to the mammalian regulatory peptides. The regulatory peptides involved were gastrin, cholecystokinin, motilin, secretin, gastric inhibitory polypeptide, pancreatic glucagon, enteroglucagon, glicentin, neurotensin, somatostatin, pancreatic polypeptide, vasoactive intestinal polypeptide, substance P, Met-enkephalin, bombesin, and β-endorphin. In the majority of the species investigated, immunoreactive epithelial endocrine cells were demonstrated with the antisera to somatostatin, gastrin, enteroglucagon, and neurotensin. Motilin-containing cells were observed in a single species, Ambystoma mexicanum. Of the peptides detected within the mammalian innervation, vasoactive intestinal polypeptide, substance P, Met-enkephalin, and β-endorphin immunoreactive nerve fibres were seen. The distribution of the immunoreactive nerves differed significantly with species. Bombesin immunoreactivity was not seen within the innervation, although a population of endocrine cells was detected within the corpus of several species. No immunoreactivity was observed with the antisera to secretin, gastric inhibitory polypeptide, or pancreatic polypeptide in the species investigated.

scholarly journals Ontogeny of Cells Containing Insulin, Glucagon, Pancreatic Polypeptide Hormone and Somatostatin in the Bovine Pancreas

1985 ◽  
Vol 38 (3) ◽  
pp. 237 ◽  
Author(s):  
SN Reddy ◽  
RB Elliott
Keyword(s):  
Pancreatic Polypeptide ◽  
Endocrine Cells ◽  
Fetal Life ◽  
Cell Type ◽  
Polypeptide Hormone ◽  
Islet Metabolism ◽  
Pancreatic Endocrine Cells ◽  
Endocrine Cell Type ◽  
Bovine Pancreas ◽  
Histochemical Procedure

Antibodies to insulin, glucagon, pancreatic polypeptide hormone (pPj and somatostatin were used in the immunofluorescence histochemical procedure to study the ontogeny of pancreatic endocrine cells containing the four hormones in the bovine fetus of approximately 100 days gestation to term. Pancreatic sections from the bovine neonate and adult were also examined for the cellular distribution of the four hormones. Immunoreactive cells staining for insulin, glucagon, PP and somatostatin were present in the pancreas of all fetuses studied. Each endocrine cell type displayed a characteristic distribution within the developing pancreas and in the neonate and adult. The presence of the four islet hormones relatively early in bovine fetal life suggests that they may be important in intra- and extra-islet metabolism in the fetus.

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