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- Publisher Website: 10.1016/j.biocel.2005.11.012
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- PMID: 16413998
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Article: Secreted PDZD2 exerts concentration-dependent effects on the proliferation of INS-1E cells
Title | Secreted PDZD2 exerts concentration-dependent effects on the proliferation of INS-1E cells |
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Authors | |
Keywords | INS-1E Insulin Pancreas PDZD2 sPDZD2 |
Issue Date | 2006 |
Publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/biocel |
Citation | International Journal Of Biochemistry And Cell Biology, 2006, v. 38 n. 5-6, p. 1015-1022 How to Cite? |
Abstract | PDZD2 (PDZ domain containing 2) is a multi-PDZ protein expressed in pancreas and many other tissues. PDZD2 shows extensive homology to pro-interleukin-16 (pro-IL-16) and is localized mainly to the endoplasmic reticulum. We have recently demonstrated that PDZD2, like pro-IL-16, is proteolytically cleaved at its C-terminus to generate a secreted protein, sPDZD2 (for secreted PDZD2). To understand the possible functional role of PDZD2 in pancreas, we investigated the cellular distribution of PDZD2 in adult pancreas using an antiserum that recognizes both the full-length and secreted forms of PDZD2. Immunohistochemical analysis revealed a strong expression of PDZD2 in pancreatic islet β cells but not α cells. Consistent with the β-cell-enriched expression of PDZD2, immunoblot analysis indicated expression of both full-length PDZD2 and sPDZD2 in the insulinoma cell line INS-1E. A recombinant sPDZD2 protein was synthesized for study of its functional effect on INS-1E cells. In culture media with limiting serum, co-incubation with sPDZD2 stimulated the proliferation of INS-1E cells. The mitogenic effect of sPDZD2 was concentration-dependent, and was associated with a slight inhibition of the insulin promoter activity at high sPDZD2 concentrations. As a potential mitogen of β-like cells, sPDZD2 may be useful for the optimization of β-cell growth and differentiation in vitro. © 2005 Elsevier Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/91712 |
ISSN | 2023 Impact Factor: 3.4 2023 SCImago Journal Rankings: 1.079 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ma, RYM | en_HK |
dc.contributor.author | Tam, TSM | en_HK |
dc.contributor.author | Suen, APM | en_HK |
dc.contributor.author | Yeung, PML | en_HK |
dc.contributor.author | Tsang, SW | en_HK |
dc.contributor.author | Chung, SK | en_HK |
dc.contributor.author | Thomas, MK | en_HK |
dc.contributor.author | Leung, PS | en_HK |
dc.contributor.author | Yao, KM | en_HK |
dc.date.accessioned | 2010-09-17T10:24:05Z | - |
dc.date.available | 2010-09-17T10:24:05Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | International Journal Of Biochemistry And Cell Biology, 2006, v. 38 n. 5-6, p. 1015-1022 | en_HK |
dc.identifier.issn | 1357-2725 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/91712 | - |
dc.description.abstract | PDZD2 (PDZ domain containing 2) is a multi-PDZ protein expressed in pancreas and many other tissues. PDZD2 shows extensive homology to pro-interleukin-16 (pro-IL-16) and is localized mainly to the endoplasmic reticulum. We have recently demonstrated that PDZD2, like pro-IL-16, is proteolytically cleaved at its C-terminus to generate a secreted protein, sPDZD2 (for secreted PDZD2). To understand the possible functional role of PDZD2 in pancreas, we investigated the cellular distribution of PDZD2 in adult pancreas using an antiserum that recognizes both the full-length and secreted forms of PDZD2. Immunohistochemical analysis revealed a strong expression of PDZD2 in pancreatic islet β cells but not α cells. Consistent with the β-cell-enriched expression of PDZD2, immunoblot analysis indicated expression of both full-length PDZD2 and sPDZD2 in the insulinoma cell line INS-1E. A recombinant sPDZD2 protein was synthesized for study of its functional effect on INS-1E cells. In culture media with limiting serum, co-incubation with sPDZD2 stimulated the proliferation of INS-1E cells. The mitogenic effect of sPDZD2 was concentration-dependent, and was associated with a slight inhibition of the insulin promoter activity at high sPDZD2 concentrations. As a potential mitogen of β-like cells, sPDZD2 may be useful for the optimization of β-cell growth and differentiation in vitro. © 2005 Elsevier Ltd. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/biocel | en_HK |
dc.relation.ispartof | International Journal of Biochemistry and Cell Biology | en_HK |
dc.subject | INS-1E | en_HK |
dc.subject | Insulin | en_HK |
dc.subject | Pancreas | en_HK |
dc.subject | PDZD2 | en_HK |
dc.subject | sPDZD2 | en_HK |
dc.subject.mesh | Adaptor Proteins, Signal Transducing | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Cell Line, Tumor | en_HK |
dc.subject.mesh | Cell Proliferation - drug effects | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Insulin-Secreting Cells - metabolism | en_HK |
dc.subject.mesh | Intracellular Signaling Peptides and Proteins - physiology - secretion | en_HK |
dc.subject.mesh | Mitogens - pharmacology | en_HK |
dc.subject.mesh | Neoplasm Proteins | en_HK |
dc.subject.mesh | Pancreas - metabolism | en_HK |
dc.title | Secreted PDZD2 exerts concentration-dependent effects on the proliferation of INS-1E cells | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Yeung, PML:pmlyeung@hku.hk | en_HK |
dc.identifier.email | Chung, SK:skchung@hkucc.hku.hk | en_HK |
dc.identifier.email | Yao, KM:kmyao@hku.hk | en_HK |
dc.identifier.authority | Yeung, PML=rp01402 | en_HK |
dc.identifier.authority | Chung, SK=rp00381 | en_HK |
dc.identifier.authority | Yao, KM=rp00344 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.biocel.2005.11.012 | en_HK |
dc.identifier.pmid | 16413998 | - |
dc.identifier.scopus | eid_2-s2.0-33644836284 | en_HK |
dc.identifier.hkuros | 119609 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33644836284&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 38 | en_HK |
dc.identifier.issue | 5-6 | en_HK |
dc.identifier.spage | 1015 | en_HK |
dc.identifier.epage | 1022 | en_HK |
dc.identifier.isi | WOS:000236525800031 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Ma, RYM=8323783700 | en_HK |
dc.identifier.scopusauthorid | Tam, TSM=12772669500 | en_HK |
dc.identifier.scopusauthorid | Suen, APM=12773296100 | en_HK |
dc.identifier.scopusauthorid | Yeung, PML=8350940900 | en_HK |
dc.identifier.scopusauthorid | Tsang, SW=8050597200 | en_HK |
dc.identifier.scopusauthorid | Chung, SK=7404292976 | en_HK |
dc.identifier.scopusauthorid | Thomas, MK=7404754193 | en_HK |
dc.identifier.scopusauthorid | Leung, PS=7401748938 | en_HK |
dc.identifier.scopusauthorid | Yao, KM=7403234578 | en_HK |
dc.identifier.issnl | 1357-2725 | - |