دورية أكاديمية

Insulinoma-derived pseudo-islets for diabetes research.

التفاصيل البيبلوغرافية
العنوان: Insulinoma-derived pseudo-islets for diabetes research.
المؤلفون: Hart NJ; Department of Surgery, University of Arizona, Tucson, Arizona., Weber C; Department of Physiology, University of Arizona, Tucson, Arizona., Price N; Department of Surgery, University of Arizona, Tucson, Arizona., Banuelos A; Department of Surgery, University of Arizona, Tucson, Arizona., Schultz M; Department of Surgery, University of Arizona, Tucson, Arizona., Huey B; Department of Surgery, University of Arizona, Tucson, Arizona., Harnois E; Department of Physiology, University of Arizona, Tucson, Arizona., Gibson C; Department of Surgery, University of Arizona, Tucson, Arizona., Steyn LV; Department of Surgery, University of Arizona, Tucson, Arizona., Papas KK; Department of Surgery, University of Arizona, Tucson, Arizona.; Department of Biomedical Engineering, University of Arizona, Tucson, Arizona.; The BIO5 Institute, University of Arizona, Tucson, Arizona., Lynch RM; Department of Physiology, University of Arizona, Tucson, Arizona.; Department of Biomedical Engineering, University of Arizona, Tucson, Arizona.; The BIO5 Institute, University of Arizona, Tucson, Arizona.
المصدر: American journal of physiology. Cell physiology [Am J Physiol Cell Physiol] 2021 Aug 01; Vol. 321 (2), pp. C247-C256. Date of Electronic Publication: 2021 Jun 09.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: American Physiological Society Country of Publication: United States NLM ID: 100901225 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1522-1563 (Electronic) Linking ISSN: 03636143 NLM ISO Abbreviation: Am J Physiol Cell Physiol Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Bethesda, Md. : American Physiological Society,
مواضيع طبية MeSH: Diabetes Mellitus/*metabolism , Insulinoma/*metabolism , Islets of Langerhans/*metabolism , Pancreas/*metabolism, Animals ; Cell Line ; Glucose/metabolism ; Insulin Secretion/physiology ; Insulin-Secreting Cells/metabolism ; Oxygen Consumption/physiology
مستخلص: The islets of Langerhans of the pancreas are the primary endocrine organ responsible for regulating whole body glucose homeostasis. The use of isolated primary islets for research development and training requires organ resection, careful digestion, and isolation of the islets from nonendocrine tissue. This process is time consuming, expensive, and requires substantial expertise. For these reasons, we sought to develop a more rapidly obtainable and consistent model system with characteristic islet morphology and function that could be employed to train personnel and better inform experiments prior to using isolated rodent and human islets. Immortalized β cell lines reflect several aspects of primary β cells, but cell propagation in monolayer cell culture limits their usefulness in several areas of research, which depend on islet morphology and/or functional assessment. In this manuscript, we describe the propagation and characterization of insulinoma pseudo-islets (IPIs) from a rat insulinoma cell line INS832/3. IPIs were generated with an average diameter of 200 μm, consistent with general islet morphology. The rates of oxygen consumption and mitochondrial oxidation-reduction changes in response to glucose and metabolic modulators were similar to isolated rat islets. In addition, the dynamic insulin secretory patterns of IPIs were similar to primary rat islets. Thus, INS832/3-derived IPIs provide a valuable and convenient model for accelerating islet and diabetes research.
References: Biochem J. 1966 Jan;98(1):7C-9C. (PMID: 5328169)
Diabetes. 2000 Mar;49(3):424-30. (PMID: 10868964)
Proc Natl Acad Sci U S A. 1988 Dec;85(23):9037-41. (PMID: 2848253)
Transplantation. 2018 Aug;102(8):1223-1229. (PMID: 29781950)
Biomacromolecules. 2010 Mar 8;11(3):610-6. (PMID: 20108955)
J Am Coll Surg. 2012 Apr;214(4):409-24; discussion 424-6. (PMID: 22397977)
Free Radic Biol Med. 2016 Nov;100:53-65. (PMID: 27519271)
J Clin Invest. 2014 May;124(5):2087-98. (PMID: 24667639)
Mol Cell Endocrinol. 2018 Sep 15;473:136-145. (PMID: 29360563)
PLoS One. 2012;7(5):e33023. (PMID: 22606219)
Proc Natl Acad Sci U S A. 1977 Feb;74(2):628-32. (PMID: 191819)
Endocrinology. 1990 Dec;127(6):2779-88. (PMID: 1701127)
Diabetologia. 1980 May;18(5):395-405. (PMID: 6775999)
Biotechnol Prog. 2014 Jan-Feb;30(1):178-87. (PMID: 24265060)
Integr Biol (Camb). 2019 Nov 30;11(8):331-341. (PMID: 31724717)
Endocrine. 2016 Mar;51(3):440-7. (PMID: 26227244)
BMC Med Genomics. 2009 Jan 15;2:3. (PMID: 19146692)
Transplant Proc. 2014 Jul-Aug;46(6):1985-8. (PMID: 25131089)
Am J Transplant. 2007 Mar;7(3):707-13. (PMID: 17229069)
Diabetes Care. 2016 Jul;39(7):1230-40. (PMID: 27208344)
J Clin Invest. 2011 Sep;121(9):3589-97. (PMID: 21865645)
Biomaterials. 2013 Jul;34(23):5785-91. (PMID: 23642538)
Endocrinology. 1990 Jul;127(1):126-32. (PMID: 2163307)
J Pharmacol Toxicol Methods. 2016 Nov - Dec;82:83-89. (PMID: 27554916)
Nat Commun. 2019 Jun 6;10(1):2474. (PMID: 31171772)
Endocrinology. 1992 Jan;130(1):167-78. (PMID: 1370150)
J Diabetes Res. 2016;2016:7625947. (PMID: 27872862)
Regen Ther. 2018 Feb 04;8:29-37. (PMID: 30271863)
J Biol Chem. 2004 Jul 23;279(30):31780-7. (PMID: 15148320)
Pancreas. 2010 Oct;39(7):1016-23. (PMID: 20467348)
Mol Metab. 2015 Oct 20;4(12):916-25. (PMID: 26909308)
Tissue Eng Part A. 2008 Mar;14(3):433-40. (PMID: 18333795)
Am J Physiol. 1998 Dec;275(6):E1100-6. (PMID: 9843754)
Biochem Biophys Res Commun. 2011 Nov 11;415(1):30-5. (PMID: 22008547)
Biotechnol Bioeng. 2007 Dec 1;98(5):1071-82. (PMID: 17497731)
J Biol Chem. 2014 Mar 28;289(13):9182-94. (PMID: 24554722)
Biochem Biophys Res Commun. 2006 Apr 28;343(1):99-104. (PMID: 16529716)
Diabetes. 2016 Nov;65(11):3418-3428. (PMID: 27465220)
Pancreas. 2018 May/Jun;47(5):533-543. (PMID: 29621044)
Biochim Biophys Acta. 1996 Mar 28;1273(3):263-7. (PMID: 8616161)
J Clin Endocrinol Metab. 2012 Sep;97(9):3197-206. (PMID: 22745242)
Transplantation. 1987 May;43(5):725-30. (PMID: 3033857)
Cell Transplant. 2012;21(12):2797-804. (PMID: 22943589)
Am J Physiol. 1997 Nov;273(5):C1613-22. (PMID: 9374647)
Am J Physiol Cell Physiol. 2019 Jan 1;316(1):C48-C56. (PMID: 30404557)
J Biotechnol. 2011 Feb 10;151(3):278-86. (PMID: 21185337)
Int J Artif Organs. 2018 Mar;41(3):152-159. (PMID: 29546813)
Biochem J. 1983 Feb 15;210(2):345-52. (PMID: 6134520)
ALTEX. 2010;27(2):105-13. (PMID: 20686743)
J Biol Chem. 2004 Oct 22;279(43):44370-5. (PMID: 15304488)
J Vis Exp. 2016 Sep 25;(115):. (PMID: 27768027)
CellR4 Repair Replace Regen Reprogram. 2015;3(1):. (PMID: 30613700)
معلومات مُعتمدة: DP3 DK106933 United States DK NIDDK NIH HHS; 1DP3DK106933-01 HHS | National Institutes of Health (NIH)
فهرسة مساهمة: Keywords: diabetes; insulin; organoids; pseudo-islet; β cell
المشرفين على المادة: IY9XDZ35W2 (Glucose)
تواريخ الأحداث: Date Created: 20210609 Date Completed: 20210922 Latest Revision: 20220802
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC8424674
DOI: 10.1152/ajpcell.00466.2020
PMID: 34106785
قاعدة البيانات: MEDLINE
الوصف
تدمد:1522-1563
DOI:10.1152/ajpcell.00466.2020