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Fluorescent protein...
Fluorescent protein vectors for pancreatic islet cell identification in live-cell imaging
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- Shuai, Hongyan (author)
- Uppsala universitet,Institutionen för medicinsk cellbiologi
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- Xu, Yunjian (author)
- Uppsala universitet,Institutionen för medicinsk cellbiologi
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- Yu, Qian (author)
- Uppsala universitet,Institutionen för medicinsk cellbiologi
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- Gylfe, Erik (author)
- Uppsala universitet,Institutionen för medicinsk cellbiologi
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- Tengholm, Anders (author)
- Uppsala universitet,Institutionen för medicinsk cellbiologi
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(creator_code:org_t)
- 2016-08-18
- 2016
- English.
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In: Pflügers Archiv. - : Springer Science and Business Media LLC. - 0031-6768 .- 1432-2013. ; 468:10, s. 1765-1777
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Abstract
Subject headings
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- The islets of Langerhans contain different types of endocrine cells, which are crucial for glucose homeostasis. beta- and alpha-cells that release insulin and glucagon, respectively, are most abundant, whereas somatostatin-producing delta-cells and particularly pancreatic polypeptide-releasing PP-cells are more scarce. Studies of islet cell function are hampered by difficulties to identify the different cell types, especially in live-cell imaging experiments when immunostaining is unsuitable. The aim of the present study was to create a set of vectors for fluorescent protein expression with cell-type-specific promoters and evaluate their applicability in functional islet imaging. We constructed six adenoviral vectors for expression of red and green fluorescent proteins controlled by the insulin, preproglucagon, somatostatin, or pancreatic polypeptide promoters. After transduction of mouse and human islets or dispersed islet cells, a majority of the fluorescent cells also immunostained for the appropriate hormone. Recordings of the sub-plasma membrane Ca2+ and cAMP concentrations with a fluorescent indicator and a protein biosensor, respectively, showed that labeled cells respond to glucose and other modulators of secretion and revealed a striking variability in Ca2+ signaling among alpha-cells. The measurements allowed comparison of the phase relationship of Ca2+ oscillations between different types of cells within intact islets. We conclude that the fluorescent protein vectors allow easy identification of specific islet cell types and can be used in live-cell imaging together with organic dyes and genetically encoded biosensors. This approach will facilitate studies of normal islet physiology and help to clarify molecular defects and disturbed cell interactions in diabetic islets.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Fysiologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Physiology (hsv//eng)
Keyword
- Islets
- alpha-cell
- beta-cell
- delta-cell
- PP-cell
- Insulin
- Glucagon
- Somatostatin
- Pancreatic polypeptide
- Ca2
- cAMP
Publication and Content Type
- ref (subject category)
- art (subject category)
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