Bariatric surgery induces pancreatic cell transdifferentiation as indicated by single‐cell transcriptomics in Zucker diabetic rats
Aims Bariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still largely unknown. The present study aims to clarify how bariatric surgery modifies pancreatic cell subgroup differentiation and transformation in...
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Published in | Journal of diabetes Vol. 16; no. 8; pp. e13521 - n/a |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Melbourne
Wiley Publishing Asia Pty Ltd
01.08.2024
John Wiley & Sons, Inc Wiley |
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Abstract | Aims
Bariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still largely unknown. The present study aims to clarify how bariatric surgery modifies pancreatic cell subgroup differentiation and transformation in the single‐cell RNA level.
Methods
Male, 8‐week‐old Zucker diabetic fatty (ZDF) rats with obesity and diabetes phenotypes were randomized into sleeve gastrectomy (Sleeve, n = 9), Roux‐en‐Y gastric bypass (RYGB, n = 9), and Sham (n = 7) groups. Two weeks after surgery, the pancreas specimen was further analyzed using single‐cell RNA‐sequencing technique.
Results
Two weeks after surgery, compared to the Sham group, the metabolic parameters including fasting plasma glucose, plasma insulin, and oral glucose tolerance test values were dramatically improved after RYGB and Sleeve procedures (p < .05) as predicted. In addition, RYGB and Sleeve groups increased the proportion of pancreatic β cells and reduced the ratio of α cells. Two multiple hormone‐expressing cells were identified, the Gcg+/Ppy + and Ins+/Gcg+/Ppy + cells. The pancreatic Ins+/Gcg+/Ppy + cells were defined for the first time, and further investigation indicates similarities with α and β cells, with unique gene expression patterns, which implies that pancreatic cell transdifferentiation occurs following bariatric surgery.
Conclusions
For the first time, using the single‐cell transcriptome map of ZDF rats, we reported a comprehensive characterization of the heterogeneity and differentiation of pancreatic endocrinal cells after bariatric surgery, which may contribute to the underlying mechanisms. Further studies will be needed to elucidate these results.
Highlights
The single‐cell transcriptome map of Zucker diabetic fatty rats' pancreatic endocrine cells after bariatric surgery were reported for the first time.
An increased ratio of pancreatic β cells, which is associated with other pancreatic endocrine cell types transdifferentiated into β cells, was observed following bariatric surgery.
For the first time, we identify the elevation of cells in the pancreas following bariatric surgery, which is indirect evidence to support the existence of transdifferentiation. |
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AbstractList | Bariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still largely unknown. The present study aims to clarify how bariatric surgery modifies pancreatic cell subgroup differentiation and transformation in the single-cell RNA level.
Male, 8-week-old Zucker diabetic fatty (ZDF) rats with obesity and diabetes phenotypes were randomized into sleeve gastrectomy (Sleeve, n = 9), Roux-en-Y gastric bypass (RYGB, n = 9), and Sham (n = 7) groups. Two weeks after surgery, the pancreas specimen was further analyzed using single-cell RNA-sequencing technique.
Two weeks after surgery, compared to the Sham group, the metabolic parameters including fasting plasma glucose, plasma insulin, and oral glucose tolerance test values were dramatically improved after RYGB and Sleeve procedures (p < .05) as predicted. In addition, RYGB and Sleeve groups increased the proportion of pancreatic β cells and reduced the ratio of α cells. Two multiple hormone-expressing cells were identified, the Gcg+/Ppy + and Ins+/Gcg+/Ppy + cells. The pancreatic Ins+/Gcg+/Ppy + cells were defined for the first time, and further investigation indicates similarities with α and β cells, with unique gene expression patterns, which implies that pancreatic cell transdifferentiation occurs following bariatric surgery.
For the first time, using the single-cell transcriptome map of ZDF rats, we reported a comprehensive characterization of the heterogeneity and differentiation of pancreatic endocrinal cells after bariatric surgery, which may contribute to the underlying mechanisms. Further studies will be needed to elucidate these results. Bariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still largely unknown. The present study aims to clarify how bariatric surgery modifies pancreatic cell subgroup differentiation and transformation in the single-cell RNA level.AIMSBariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still largely unknown. The present study aims to clarify how bariatric surgery modifies pancreatic cell subgroup differentiation and transformation in the single-cell RNA level.Male, 8-week-old Zucker diabetic fatty (ZDF) rats with obesity and diabetes phenotypes were randomized into sleeve gastrectomy (Sleeve, n = 9), Roux-en-Y gastric bypass (RYGB, n = 9), and Sham (n = 7) groups. Two weeks after surgery, the pancreas specimen was further analyzed using single-cell RNA-sequencing technique.METHODSMale, 8-week-old Zucker diabetic fatty (ZDF) rats with obesity and diabetes phenotypes were randomized into sleeve gastrectomy (Sleeve, n = 9), Roux-en-Y gastric bypass (RYGB, n = 9), and Sham (n = 7) groups. Two weeks after surgery, the pancreas specimen was further analyzed using single-cell RNA-sequencing technique.Two weeks after surgery, compared to the Sham group, the metabolic parameters including fasting plasma glucose, plasma insulin, and oral glucose tolerance test values were dramatically improved after RYGB and Sleeve procedures (p < .05) as predicted. In addition, RYGB and Sleeve groups increased the proportion of pancreatic β cells and reduced the ratio of α cells. Two multiple hormone-expressing cells were identified, the Gcg+/Ppy + and Ins+/Gcg+/Ppy + cells. The pancreatic Ins+/Gcg+/Ppy + cells were defined for the first time, and further investigation indicates similarities with α and β cells, with unique gene expression patterns, which implies that pancreatic cell transdifferentiation occurs following bariatric surgery.RESULTSTwo weeks after surgery, compared to the Sham group, the metabolic parameters including fasting plasma glucose, plasma insulin, and oral glucose tolerance test values were dramatically improved after RYGB and Sleeve procedures (p < .05) as predicted. In addition, RYGB and Sleeve groups increased the proportion of pancreatic β cells and reduced the ratio of α cells. Two multiple hormone-expressing cells were identified, the Gcg+/Ppy + and Ins+/Gcg+/Ppy + cells. The pancreatic Ins+/Gcg+/Ppy + cells were defined for the first time, and further investigation indicates similarities with α and β cells, with unique gene expression patterns, which implies that pancreatic cell transdifferentiation occurs following bariatric surgery.For the first time, using the single-cell transcriptome map of ZDF rats, we reported a comprehensive characterization of the heterogeneity and differentiation of pancreatic endocrinal cells after bariatric surgery, which may contribute to the underlying mechanisms. Further studies will be needed to elucidate these results.CONCLUSIONSFor the first time, using the single-cell transcriptome map of ZDF rats, we reported a comprehensive characterization of the heterogeneity and differentiation of pancreatic endocrinal cells after bariatric surgery, which may contribute to the underlying mechanisms. Further studies will be needed to elucidate these results. AimsBariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still largely unknown. The present study aims to clarify how bariatric surgery modifies pancreatic cell subgroup differentiation and transformation in the single‐cell RNA level.MethodsMale, 8‐week‐old Zucker diabetic fatty (ZDF) rats with obesity and diabetes phenotypes were randomized into sleeve gastrectomy (Sleeve, n = 9), Roux‐en‐Y gastric bypass (RYGB, n = 9), and Sham (n = 7) groups. Two weeks after surgery, the pancreas specimen was further analyzed using single‐cell RNA‐sequencing technique.ResultsTwo weeks after surgery, compared to the Sham group, the metabolic parameters including fasting plasma glucose, plasma insulin, and oral glucose tolerance test values were dramatically improved after RYGB and Sleeve procedures (p < .05) as predicted. In addition, RYGB and Sleeve groups increased the proportion of pancreatic β cells and reduced the ratio of α cells. Two multiple hormone‐expressing cells were identified, the Gcg+/Ppy + and Ins+/Gcg+/Ppy + cells. The pancreatic Ins+/Gcg+/Ppy + cells were defined for the first time, and further investigation indicates similarities with α and β cells, with unique gene expression patterns, which implies that pancreatic cell transdifferentiation occurs following bariatric surgery.ConclusionsFor the first time, using the single‐cell transcriptome map of ZDF rats, we reported a comprehensive characterization of the heterogeneity and differentiation of pancreatic endocrinal cells after bariatric surgery, which may contribute to the underlying mechanisms. Further studies will be needed to elucidate these results. Aims Bariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still largely unknown. The present study aims to clarify how bariatric surgery modifies pancreatic cell subgroup differentiation and transformation in the single‐cell RNA level. Methods Male, 8‐week‐old Zucker diabetic fatty (ZDF) rats with obesity and diabetes phenotypes were randomized into sleeve gastrectomy (Sleeve, n = 9), Roux‐en‐Y gastric bypass (RYGB, n = 9), and Sham (n = 7) groups. Two weeks after surgery, the pancreas specimen was further analyzed using single‐cell RNA‐sequencing technique. Results Two weeks after surgery, compared to the Sham group, the metabolic parameters including fasting plasma glucose, plasma insulin, and oral glucose tolerance test values were dramatically improved after RYGB and Sleeve procedures (p < .05) as predicted. In addition, RYGB and Sleeve groups increased the proportion of pancreatic β cells and reduced the ratio of α cells. Two multiple hormone‐expressing cells were identified, the Gcg+/Ppy + and Ins+/Gcg+/Ppy + cells. The pancreatic Ins+/Gcg+/Ppy + cells were defined for the first time, and further investigation indicates similarities with α and β cells, with unique gene expression patterns, which implies that pancreatic cell transdifferentiation occurs following bariatric surgery. Conclusions For the first time, using the single‐cell transcriptome map of ZDF rats, we reported a comprehensive characterization of the heterogeneity and differentiation of pancreatic endocrinal cells after bariatric surgery, which may contribute to the underlying mechanisms. Further studies will be needed to elucidate these results. Highlights The single‐cell transcriptome map of Zucker diabetic fatty rats' pancreatic endocrine cells after bariatric surgery were reported for the first time. An increased ratio of pancreatic β cells, which is associated with other pancreatic endocrine cell types transdifferentiated into β cells, was observed following bariatric surgery. For the first time, we identify the elevation of cells in the pancreas following bariatric surgery, which is indirect evidence to support the existence of transdifferentiation. Highlights The single‐cell transcriptome map of Zucker diabetic fatty rats' pancreatic endocrine cells after bariatric surgery were reported for the first time. An increased ratio of pancreatic β cells, which is associated with other pancreatic endocrine cell types transdifferentiated into β cells, was observed following bariatric surgery. For the first time, we identify the elevation of cells in the pancreas following bariatric surgery, which is indirect evidence to support the existence of transdifferentiation. Abstract Aims Bariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still largely unknown. The present study aims to clarify how bariatric surgery modifies pancreatic cell subgroup differentiation and transformation in the single‐cell RNA level. Methods Male, 8‐week‐old Zucker diabetic fatty (ZDF) rats with obesity and diabetes phenotypes were randomized into sleeve gastrectomy (Sleeve, n = 9), Roux‐en‐Y gastric bypass (RYGB, n = 9), and Sham (n = 7) groups. Two weeks after surgery, the pancreas specimen was further analyzed using single‐cell RNA‐sequencing technique. Results Two weeks after surgery, compared to the Sham group, the metabolic parameters including fasting plasma glucose, plasma insulin, and oral glucose tolerance test values were dramatically improved after RYGB and Sleeve procedures (p < .05) as predicted. In addition, RYGB and Sleeve groups increased the proportion of pancreatic β cells and reduced the ratio of α cells. Two multiple hormone‐expressing cells were identified, the Gcg+/Ppy + and Ins+/Gcg+/Ppy + cells. The pancreatic Ins+/Gcg+/Ppy + cells were defined for the first time, and further investigation indicates similarities with α and β cells, with unique gene expression patterns, which implies that pancreatic cell transdifferentiation occurs following bariatric surgery. Conclusions For the first time, using the single‐cell transcriptome map of ZDF rats, we reported a comprehensive characterization of the heterogeneity and differentiation of pancreatic endocrinal cells after bariatric surgery, which may contribute to the underlying mechanisms. Further studies will be needed to elucidate these results. |
Author | Li, Mengyi Liang, Yongjun Qiao, Zhengdong Wang, Yueqian Zhang, Peng Gu, Yan Yang, Jianjun Widjaja, Jason Zhang, Zhongtao Sun, Jiawei Cao, Ting Zhang, Xiong |
AuthorAffiliation | 1 Center for Medical Research and Innovation, Shanghai Pudong Hospital Fudan University Pudong Medical Center Shanghai China 4 Department of Bariatric and Metabolic Surgery Fudan University Affiliated Huadong Hospital Shanghai China 3 Shanghai Key Laboratory of Vascular Lesions Regulation and Remodeling Shanghai China 5 Novogene Bioinformatics Institute Beijing China 2 Fudan Zhangjiang Institute Fudan University Shanghai China 6 Division of Metabolic and Bariatric Surgery, General Surgery Center, Beijing Friendship Hospital Capital Medical University Beijing China 7 National Clinical Research Center for Digestive Diseases Beijing China |
AuthorAffiliation_xml | – name: 5 Novogene Bioinformatics Institute Beijing China – name: 7 National Clinical Research Center for Digestive Diseases Beijing China – name: 6 Division of Metabolic and Bariatric Surgery, General Surgery Center, Beijing Friendship Hospital Capital Medical University Beijing China – name: 3 Shanghai Key Laboratory of Vascular Lesions Regulation and Remodeling Shanghai China – name: 1 Center for Medical Research and Innovation, Shanghai Pudong Hospital Fudan University Pudong Medical Center Shanghai China – name: 4 Department of Bariatric and Metabolic Surgery Fudan University Affiliated Huadong Hospital Shanghai China – name: 2 Fudan Zhangjiang Institute Fudan University Shanghai China |
Author_xml | – sequence: 1 givenname: Yongjun surname: Liang fullname: Liang, Yongjun organization: Shanghai Key Laboratory of Vascular Lesions Regulation and Remodeling – sequence: 2 givenname: Jason orcidid: 0000-0003-0103-6147 surname: Widjaja fullname: Widjaja, Jason organization: Fudan University Affiliated Huadong Hospital – sequence: 3 givenname: Jiawei surname: Sun fullname: Sun, Jiawei organization: Novogene Bioinformatics Institute – sequence: 4 givenname: Mengyi surname: Li fullname: Li, Mengyi organization: National Clinical Research Center for Digestive Diseases – sequence: 5 givenname: Zhengdong surname: Qiao fullname: Qiao, Zhengdong organization: Fudan University Pudong Medical Center – sequence: 6 givenname: Ting surname: Cao fullname: Cao, Ting organization: Fudan University Pudong Medical Center – sequence: 7 givenname: Yueqian surname: Wang fullname: Wang, Yueqian organization: Fudan University Pudong Medical Center – sequence: 8 givenname: Xiong surname: Zhang fullname: Zhang, Xiong organization: Fudan University Pudong Medical Center – sequence: 9 givenname: Zhongtao surname: Zhang fullname: Zhang, Zhongtao organization: National Clinical Research Center for Digestive Diseases – sequence: 10 givenname: Yan surname: Gu fullname: Gu, Yan organization: Fudan University Affiliated Huadong Hospital – sequence: 11 givenname: Peng orcidid: 0000-0002-2194-8760 surname: Zhang fullname: Zhang, Peng email: zhangpg@yahoo.com organization: National Clinical Research Center for Digestive Diseases – sequence: 12 givenname: Jianjun surname: Yang fullname: Yang, Jianjun email: ayang1230@126.com organization: Fudan University Affiliated Huadong Hospital |
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Copyright | 2024 The Author(s). published by Ruijin Hospital, Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd. 2024 The Author(s). Journal of Diabetes published by Ruijin Hospital, Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd. 2024. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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Keywords | type 2 diabetes mellitus pancreatic cell differentiation bariatric surgery |
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Snippet | Aims
Bariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still... Bariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still largely... AimsBariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are still... Highlights The single‐cell transcriptome map of Zucker diabetic fatty rats' pancreatic endocrine cells after bariatric surgery were reported for the first... Abstract Aims Bariatric surgery results in rapid recovery of glucose control in subjects with type 2 diabetes mellitus. However, the underlying mechanisms are... |
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SubjectTerms | Animals bariatric surgery Bariatric Surgery - methods Blood Glucose - metabolism Cell Transdifferentiation - genetics Diabetes Diabetes Mellitus, Experimental - genetics Diabetes Mellitus, Experimental - metabolism Diabetes Mellitus, Experimental - surgery Diabetes Mellitus, Type 2 - genetics Diabetes Mellitus, Type 2 - metabolism Diabetes Mellitus, Type 2 - surgery Gastrointestinal surgery Glucose Insulin-Secreting Cells - metabolism Insulin-Secreting Cells - pathology Male Obesity - genetics Obesity - metabolism Obesity - surgery Original Pancreas - metabolism Pancreas - pathology pancreatic cell differentiation Rats Rats, Zucker Single-Cell Analysis - methods Transcriptome type 2 diabetes mellitus |
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Title | Bariatric surgery induces pancreatic cell transdifferentiation as indicated by single‐cell transcriptomics in Zucker diabetic rats |
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