Quantitative, in situ visualization of intracellular insulin vesicles in pancreatic beta cells

Author:

Guo Amin12,Zhang Jianhua12ORCID,He Bo12ORCID,Li Angdi3ORCID,Sun Tianxiao45,Li Weimin3,Wang Jian4ORCID,Tai Renzhong6,Liu Yan3ORCID,Qian Zhen3,Fan Jiadong12,Sali Andrej78ORCID,Stevens Raymond C.3910,Jiang Huaidong12ORCID

Affiliation:

1. Center for Transformative Science, ShanghaiTech University, Shanghai 201210, China

2. School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China

3. iHuman Institute, School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China

4. Canadian Light Source Inc., University of Saskatchewan, Saskatoon, SK S7N 2V3, Canada

5. Helmholtz-Zentrum Berlin für Materialien und Energie, 12489 Berlin, Germany

6. Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Chinese Academy of Science, Shanghai 201204, China

7. California Institute for Quantitative Biosciences, Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA 94158

8. Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94158

9. Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089

10. Bridge Institute, USC Michelson Center for Convergent Bioscience, University of Southern California, Los Angeles, CA 90089

Abstract

Characterizing relationships between Zn 2+ , insulin, and insulin vesicles is of vital importance to the study of pancreatic beta cells. However, the precise content of Zn 2+ and the specific location of insulin inside insulin vesicles are not clear, which hinders a thorough understanding of the insulin secretion process and diseases caused by blood sugar dysregulation. Here, we demonstrated the colocalization of Zn 2+ and insulin in both single extracellular insulin vesicles and pancreatic beta cells by using an X-ray scanning coherent diffraction imaging (ptychography) technique. We also analyzed the elemental Zn 2+ and Ca 2+ contents of insulin vesicles using electron microscopy and energy dispersive spectroscopy (EDS) mapping. We found that the presence of Zn 2+ is an important characteristic that can be used to distinguish insulin vesicles from other types of vesicles in pancreatic beta cells and that the content of Zn 2+ is proportional to the size of insulin vesicles. By using dual-energy contrast X-ray microscopy and scanning transmission X-ray microscopy (STXM) image stacks, we observed that insulin accumulates in the off-center position of extracellular insulin vesicles. Furthermore, the spatial distribution of insulin vesicles and their colocalization with other organelles inside pancreatic beta cells were demonstrated using three-dimensional (3D) imaging by combining X-ray ptychography and an equally sloped tomography (EST) algorithm. This study describes a powerful method to univocally describe the location and quantitative analysis of intracellular insulin, which will be of great significance to the study of diabetes and other blood sugar diseases.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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