Loading…
Induction of islet cell neogenesis in the adult pancreas: the partial duct obstruction model
The proliferative capacity of adult pancreatic islet cells is limited, although the formation of new islets from cells associated with the ductal epithelium is achievable even in the adult gland. Understanding the mechanism whereby proliferation and subsequent differentiation of putative precursor c...
Saved in:
Published in: | Microscopy research and technique 1998-11, Vol.43 (4), p.337-346 |
---|---|
Main Author: | |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c4718-af981608263d96159453744985ed01d3be600a856b06ce9367b505f1e52905a33 |
container_end_page | 346 |
container_issue | 4 |
container_start_page | 337 |
container_title | Microscopy research and technique |
container_volume | 43 |
creator | Rosenberg, Lawrence |
description | The proliferative capacity of adult pancreatic islet cells is limited, although the formation of new islets from cells associated with the ductal epithelium is achievable even in the adult gland. Understanding the mechanism whereby proliferation and subsequent differentiation of putative precursor cells leads the appearance of new islets, i.e., islet neogenesis, may be important as a modality for treatment of both Type I and type II diabetes, in which there is an absolute or relative deficiency of insulin. It appears that certain genes and their protein products are essential to the initiation of the initial step in the pathway. We have shown that partial obstruction of the hamster pancreas is able to reverse streptozotocin‐induced diabetes more than 50% of the time. An extract, termed ilotropin, prepared from obstructed pancreata, also reverses the diabetes, whereas extracts of control non‐obstructed pancreata do not. Ilotropin contains a protein that is heat and acid stable with MW around 20–45 kDa that is capable of stimulating the proliferation of isolated duct cells in culture. Using mRNA and a differential display technique, 20 genes were found to be expressed in the partially obstructed (regenerating), but not the non‐obstructed (non‐regenerating) pancreas. One of these islet neogenesis‐associated proteins (INGAP) proved to be unique to the obstructed pancreas, and a peptide contained within the sequence was capable of stimulating the proliferation of ductal cells in culture. INGAP was found to be expressed early in the neogenic process before the onset of ductal cell proliferation, and was capable of stimulating tritiated thymidine uptake into protodifferentiated epithelial cells, compatible with the notion that it might be involved in initiating the process of islet neogenesis. Microsc. Res. Tech. 43:337–346, 1998. © 1998 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1097-0029(19981115)43:4<337::AID-JEMT8>3.0.CO;2-U |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70119900</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70119900</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4718-af981608263d96159453744985ed01d3be600a856b06ce9367b505f1e52905a33</originalsourceid><addsrcrecordid>eNqFkMFu1DAQhiMEKm3hEZB8Qu0hyzi243hBVCW0JWhhD-yqFUIaOYlDA9lksRNB3x6nWfYCEifbM_Y3_r8gOKMwowDRi5NPWZqdUlAy9Ed1QpVKKKXilLM5f8WYnM_Ps7fh-4sPq-Q1m8EsXb6MwvWD4HD_5uG4FypUFG4eB0fOfQPwBMoPggOVcKWkOAy-ZG05FH3dtaSrSO0a05PCNA1pTffVtMbVjtQt6W8N0eXQ9GSr28Ia7eb3ta22fa0bMjJIl7ve7mCbrjTNk-BRpRtnnu7W42B9ebFK34WL5VWWni_CgkuahLry2WJIopiVKqZCccEk5yoRpgRastzEADoRcQ5xYRSLZS5AVNSISIHQjB0Hzyfu1nY_BuN63NRuTKF9isGh9LmVAvAXr6eLhe2cs6bCra032t4hBRy9I47ecXSIo0P84x05Q47eO6L3jvfekSFgusQI1578bPeFId-Ycs_difb9m6n_s27M3V9j_zv1X0OngkeHE7p2vfm1R2v7HWPJpMDrj1f4Jl1cJp9XEiX7DaO9rQA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70119900</pqid></control><display><type>article</type><title>Induction of islet cell neogenesis in the adult pancreas: the partial duct obstruction model</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Rosenberg, Lawrence</creator><creatorcontrib>Rosenberg, Lawrence</creatorcontrib><description>The proliferative capacity of adult pancreatic islet cells is limited, although the formation of new islets from cells associated with the ductal epithelium is achievable even in the adult gland. Understanding the mechanism whereby proliferation and subsequent differentiation of putative precursor cells leads the appearance of new islets, i.e., islet neogenesis, may be important as a modality for treatment of both Type I and type II diabetes, in which there is an absolute or relative deficiency of insulin. It appears that certain genes and their protein products are essential to the initiation of the initial step in the pathway. We have shown that partial obstruction of the hamster pancreas is able to reverse streptozotocin‐induced diabetes more than 50% of the time. An extract, termed ilotropin, prepared from obstructed pancreata, also reverses the diabetes, whereas extracts of control non‐obstructed pancreata do not. Ilotropin contains a protein that is heat and acid stable with MW around 20–45 kDa that is capable of stimulating the proliferation of isolated duct cells in culture. Using mRNA and a differential display technique, 20 genes were found to be expressed in the partially obstructed (regenerating), but not the non‐obstructed (non‐regenerating) pancreas. One of these islet neogenesis‐associated proteins (INGAP) proved to be unique to the obstructed pancreas, and a peptide contained within the sequence was capable of stimulating the proliferation of ductal cells in culture. INGAP was found to be expressed early in the neogenic process before the onset of ductal cell proliferation, and was capable of stimulating tritiated thymidine uptake into protodifferentiated epithelial cells, compatible with the notion that it might be involved in initiating the process of islet neogenesis. Microsc. Res. Tech. 43:337–346, 1998. © 1998 Wiley‐Liss, Inc.</description><identifier>ISSN: 1059-910X</identifier><identifier>EISSN: 1097-0029</identifier><identifier>DOI: 10.1002/(SICI)1097-0029(19981115)43:4<337::AID-JEMT8>3.0.CO;2-U</identifier><identifier>PMID: 9849975</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Antigens, Neoplasm ; beta-cell regeneration ; Biomarkers, Tumor ; Cell Differentiation ; Cellophane ; cellophane wrapping ; Cricetinae ; Diabetes Mellitus, Experimental - drug therapy ; Diabetes Mellitus, Experimental - therapy ; islet neogenesis ; Islets of Langerhans - cytology ; Islets of Langerhans - physiology ; Lectins, C-Type ; Ligation ; Mesocricetus ; Pancreatic Ducts - physiology ; Pancreatitis-Associated Proteins ; precursor cell ; Proteins - genetics ; Proteins - physiology ; Proteins - therapeutic use ; Regeneration ; Syrian golden hamster</subject><ispartof>Microscopy research and technique, 1998-11, Vol.43 (4), p.337-346</ispartof><rights>Copyright © 1998 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4718-af981608263d96159453744985ed01d3be600a856b06ce9367b505f1e52905a33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9849975$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosenberg, Lawrence</creatorcontrib><title>Induction of islet cell neogenesis in the adult pancreas: the partial duct obstruction model</title><title>Microscopy research and technique</title><addtitle>Microsc. Res. Tech</addtitle><description>The proliferative capacity of adult pancreatic islet cells is limited, although the formation of new islets from cells associated with the ductal epithelium is achievable even in the adult gland. Understanding the mechanism whereby proliferation and subsequent differentiation of putative precursor cells leads the appearance of new islets, i.e., islet neogenesis, may be important as a modality for treatment of both Type I and type II diabetes, in which there is an absolute or relative deficiency of insulin. It appears that certain genes and their protein products are essential to the initiation of the initial step in the pathway. We have shown that partial obstruction of the hamster pancreas is able to reverse streptozotocin‐induced diabetes more than 50% of the time. An extract, termed ilotropin, prepared from obstructed pancreata, also reverses the diabetes, whereas extracts of control non‐obstructed pancreata do not. Ilotropin contains a protein that is heat and acid stable with MW around 20–45 kDa that is capable of stimulating the proliferation of isolated duct cells in culture. Using mRNA and a differential display technique, 20 genes were found to be expressed in the partially obstructed (regenerating), but not the non‐obstructed (non‐regenerating) pancreas. One of these islet neogenesis‐associated proteins (INGAP) proved to be unique to the obstructed pancreas, and a peptide contained within the sequence was capable of stimulating the proliferation of ductal cells in culture. INGAP was found to be expressed early in the neogenic process before the onset of ductal cell proliferation, and was capable of stimulating tritiated thymidine uptake into protodifferentiated epithelial cells, compatible with the notion that it might be involved in initiating the process of islet neogenesis. Microsc. Res. Tech. 43:337–346, 1998. © 1998 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Antigens, Neoplasm</subject><subject>beta-cell regeneration</subject><subject>Biomarkers, Tumor</subject><subject>Cell Differentiation</subject><subject>Cellophane</subject><subject>cellophane wrapping</subject><subject>Cricetinae</subject><subject>Diabetes Mellitus, Experimental - drug therapy</subject><subject>Diabetes Mellitus, Experimental - therapy</subject><subject>islet neogenesis</subject><subject>Islets of Langerhans - cytology</subject><subject>Islets of Langerhans - physiology</subject><subject>Lectins, C-Type</subject><subject>Ligation</subject><subject>Mesocricetus</subject><subject>Pancreatic Ducts - physiology</subject><subject>Pancreatitis-Associated Proteins</subject><subject>precursor cell</subject><subject>Proteins - genetics</subject><subject>Proteins - physiology</subject><subject>Proteins - therapeutic use</subject><subject>Regeneration</subject><subject>Syrian golden hamster</subject><issn>1059-910X</issn><issn>1097-0029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkMFu1DAQhiMEKm3hEZB8Qu0hyzi243hBVCW0JWhhD-yqFUIaOYlDA9lksRNB3x6nWfYCEifbM_Y3_r8gOKMwowDRi5NPWZqdUlAy9Ed1QpVKKKXilLM5f8WYnM_Ps7fh-4sPq-Q1m8EsXb6MwvWD4HD_5uG4FypUFG4eB0fOfQPwBMoPggOVcKWkOAy-ZG05FH3dtaSrSO0a05PCNA1pTffVtMbVjtQt6W8N0eXQ9GSr28Ia7eb3ta22fa0bMjJIl7ve7mCbrjTNk-BRpRtnnu7W42B9ebFK34WL5VWWni_CgkuahLry2WJIopiVKqZCccEk5yoRpgRastzEADoRcQ5xYRSLZS5AVNSISIHQjB0Hzyfu1nY_BuN63NRuTKF9isGh9LmVAvAXr6eLhe2cs6bCra032t4hBRy9I47ecXSIo0P84x05Q47eO6L3jvfekSFgusQI1578bPeFId-Ycs_difb9m6n_s27M3V9j_zv1X0OngkeHE7p2vfm1R2v7HWPJpMDrj1f4Jl1cJp9XEiX7DaO9rQA</recordid><startdate>19981115</startdate><enddate>19981115</enddate><creator>Rosenberg, Lawrence</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19981115</creationdate><title>Induction of islet cell neogenesis in the adult pancreas: the partial duct obstruction model</title><author>Rosenberg, Lawrence</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4718-af981608263d96159453744985ed01d3be600a856b06ce9367b505f1e52905a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Antigens, Neoplasm</topic><topic>beta-cell regeneration</topic><topic>Biomarkers, Tumor</topic><topic>Cell Differentiation</topic><topic>Cellophane</topic><topic>cellophane wrapping</topic><topic>Cricetinae</topic><topic>Diabetes Mellitus, Experimental - drug therapy</topic><topic>Diabetes Mellitus, Experimental - therapy</topic><topic>islet neogenesis</topic><topic>Islets of Langerhans - cytology</topic><topic>Islets of Langerhans - physiology</topic><topic>Lectins, C-Type</topic><topic>Ligation</topic><topic>Mesocricetus</topic><topic>Pancreatic Ducts - physiology</topic><topic>Pancreatitis-Associated Proteins</topic><topic>precursor cell</topic><topic>Proteins - genetics</topic><topic>Proteins - physiology</topic><topic>Proteins - therapeutic use</topic><topic>Regeneration</topic><topic>Syrian golden hamster</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rosenberg, Lawrence</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Microscopy research and technique</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosenberg, Lawrence</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of islet cell neogenesis in the adult pancreas: the partial duct obstruction model</atitle><jtitle>Microscopy research and technique</jtitle><addtitle>Microsc. Res. Tech</addtitle><date>1998-11-15</date><risdate>1998</risdate><volume>43</volume><issue>4</issue><spage>337</spage><epage>346</epage><pages>337-346</pages><issn>1059-910X</issn><eissn>1097-0029</eissn><abstract>The proliferative capacity of adult pancreatic islet cells is limited, although the formation of new islets from cells associated with the ductal epithelium is achievable even in the adult gland. Understanding the mechanism whereby proliferation and subsequent differentiation of putative precursor cells leads the appearance of new islets, i.e., islet neogenesis, may be important as a modality for treatment of both Type I and type II diabetes, in which there is an absolute or relative deficiency of insulin. It appears that certain genes and their protein products are essential to the initiation of the initial step in the pathway. We have shown that partial obstruction of the hamster pancreas is able to reverse streptozotocin‐induced diabetes more than 50% of the time. An extract, termed ilotropin, prepared from obstructed pancreata, also reverses the diabetes, whereas extracts of control non‐obstructed pancreata do not. Ilotropin contains a protein that is heat and acid stable with MW around 20–45 kDa that is capable of stimulating the proliferation of isolated duct cells in culture. Using mRNA and a differential display technique, 20 genes were found to be expressed in the partially obstructed (regenerating), but not the non‐obstructed (non‐regenerating) pancreas. One of these islet neogenesis‐associated proteins (INGAP) proved to be unique to the obstructed pancreas, and a peptide contained within the sequence was capable of stimulating the proliferation of ductal cells in culture. INGAP was found to be expressed early in the neogenic process before the onset of ductal cell proliferation, and was capable of stimulating tritiated thymidine uptake into protodifferentiated epithelial cells, compatible with the notion that it might be involved in initiating the process of islet neogenesis. Microsc. Res. Tech. 43:337–346, 1998. © 1998 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9849975</pmid><doi>10.1002/(SICI)1097-0029(19981115)43:4<337::AID-JEMT8>3.0.CO;2-U</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1059-910X |
ispartof | Microscopy research and technique, 1998-11, Vol.43 (4), p.337-346 |
issn | 1059-910X 1097-0029 |
language | eng |
recordid | cdi_proquest_miscellaneous_70119900 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Animals Antigens, Neoplasm beta-cell regeneration Biomarkers, Tumor Cell Differentiation Cellophane cellophane wrapping Cricetinae Diabetes Mellitus, Experimental - drug therapy Diabetes Mellitus, Experimental - therapy islet neogenesis Islets of Langerhans - cytology Islets of Langerhans - physiology Lectins, C-Type Ligation Mesocricetus Pancreatic Ducts - physiology Pancreatitis-Associated Proteins precursor cell Proteins - genetics Proteins - physiology Proteins - therapeutic use Regeneration Syrian golden hamster |
title | Induction of islet cell neogenesis in the adult pancreas: the partial duct obstruction model |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T23%3A35%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Induction%20of%20islet%20cell%20neogenesis%20in%20the%20adult%20pancreas:%20the%20partial%20duct%20obstruction%20model&rft.jtitle=Microscopy%20research%20and%20technique&rft.au=Rosenberg,%20Lawrence&rft.date=1998-11-15&rft.volume=43&rft.issue=4&rft.spage=337&rft.epage=346&rft.pages=337-346&rft.issn=1059-910X&rft.eissn=1097-0029&rft_id=info:doi/10.1002/(SICI)1097-0029(19981115)43:4%3C337::AID-JEMT8%3E3.0.CO;2-U&rft_dat=%3Cproquest_cross%3E70119900%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4718-af981608263d96159453744985ed01d3be600a856b06ce9367b505f1e52905a33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=70119900&rft_id=info:pmid/9849975&rfr_iscdi=true |