Hellström-Lindahl Ewa, Danielsson Angelika, Ponten Fredrik, Czernichow Paul, Korsgren Olle, Johansson Lars, Eriksson Olof
Department of Medicinal Chemistry, Preclinical PET Platform, Uppsala University, 751 83, Uppsala, Sweden.
Department of Immunology, Genetics and Pathology, Uppsala University, 751 83, Uppsala, Sweden.
Acta Diabetol. 2016 Jun;53(3):413-21. doi: 10.1007/s00592-015-0811-3. Epub 2015 Oct 14.
To address questions regarding onset and progression of types 1 and 2 diabetes (T1D/T2D), surrogate imaging biomarkers for beta cell function and mass are needed. Here, we assess the potential of GPR44 as a surrogate marker for beta cells, in a direct comparison with clinically used biomarker VMAT2.
GPR44 surface availability was assessed by flow cytometry of human beta cells. RNA transcription levels in different pancreas compartments were evaluated. The density of GPR44 receptor in endocrine and exocrine tissues was assessed by the radiolabeled GPR44 ligand [(3)H]AZD 3825. A direct comparison with the established beta cell marker VMAT2 was performed by radiolabeled [(3)H]DTBZ.
GPR44 was available on the cell surface, and pancreatic RNA levels were restricted to the islets of Langerhans. [(3)H]AZD 3825 had nanomolar affinity for GPR44 in human islets and EndoC-βH1 beta cells, and the specific binding to human beta cells was close to 50 times higher than in exocrine preparations. The endocrine-to-exocrine binding ratio was approximately 10 times higher for [(3)H]AZD 3825 than for [(3)H]DTBZ.
GPR44 is a highly beta cell-specific target, which potentially offers improved imaging contrast between the human beta cell and the exocrine pancreas.
为解决有关1型和2型糖尿病(T1D/T2D)的发病和进展问题,需要用于β细胞功能和质量的替代成像生物标志物。在此,我们将GPR44与临床使用的生物标志物VMAT2进行直接比较,评估其作为β细胞替代标志物的潜力。
通过对人β细胞进行流式细胞术评估GPR44的表面可用性。评估不同胰腺区域的RNA转录水平。通过放射性标记的GPR44配体[(3)H]AZD 3825评估内分泌和外分泌组织中GPR44受体的密度。通过放射性标记的[(3)H]DTBZ与已确立的β细胞标志物VMAT2进行直接比较。
GPR44在细胞表面可用,胰腺RNA水平仅限于胰岛。[(3)H]AZD 3825对人胰岛和EndoC-βH1β细胞中的GPR44具有纳摩尔亲和力,与人β细胞的特异性结合比在外分泌制剂中高近50倍。[(3)H]AZD 3825的内分泌与外分泌结合比[(3)H]DTBZ高约10倍。
GPR44是一种高度β细胞特异性靶点,可能会改善人β细胞与外分泌胰腺之间的成像对比度。