Coordination between ECM and cell-cell adhesion regulates the development of islet aggregation, architecture, and functional maturation

Author:

Tixi Wilma1,Maldonado Maricela12ORCID,Chang Ya-Ting1,Chiu Amy1,Yeung Wilson1,Parveen Nazia1,Nelson Michael S3ORCID,Hart Ryan4,Wang Shihao5,Hsu Wu Jih5ORCID,Fueger Patrick6,Kopp Janel L5ORCID,Huising Mark O47,Dhawan Sangeeta1,Shih Hung Ping1ORCID

Affiliation:

1. Department of Translational Research and Cellular Therapeutics, Arthur Riggs Diabetes and Metabolism Research Institute, Beckman Research Institute, City of Hope

2. Department of Biomedical Engineering, College of Engineering, California State University, Long Beach

3. Light Microscopy Core, Beckman Research Institute, City of Hope

4. Department of Neurobiology, Physiology and Behavior, University of California, Davis

5. Department of Cellular and Physiological Sciences, Life Sciences Institute, University of British Columbia

6. Department of Molecular & Cellular Endocrinology, Arthur Riggs Diabetes and Metabolism Research Institute, Beckman Research Institute, City of Hope

7. Department of Physiology and Membrane Biology, School of Medicine, University of California, Davis

Abstract

Pancreatic islets are three-dimensional cell aggregates consisting of unique cellular composition, cell-to-cell contacts, and interactions with blood vessels. Cell aggregation is essential for islet endocrine function; however, it remains unclear how developing islets establish aggregation. By combining genetic animal models, imaging tools, and gene expression profiling, we demonstrate that islet aggregation is regulated by extracellular matrix signaling and cell-cell adhesion. Islet endocrine cell-specific inactivation of extracellular matrix receptor integrin β1 disrupted blood vessel interactions but promoted cell-cell adhesion and the formation of larger islets. In contrast, ablation of cell-cell adhesion molecule α-catenin promoted blood vessel interactions yet compromised islet clustering. Simultaneous removal of integrin β1 and α-catenin disrupts islet aggregation and the endocrine cell maturation process, demonstrating that establishment of islet aggregates is essential for functional maturation. Our study provides new insights into understanding the fundamental self-organizing mechanism for islet aggregation, architecture, and functional maturation.

Funder

California Institute for Regenerative Medicine

JDRF

Natural Sciences and Engineering Research Council of Canada

Canadian Institutes of Health Research

Michael Smith Foundation for Health Research

National Institute of Diabetes and Digestive and Kidney Diseases

Human Islet Research Network

Wanek Family Foundation to Cure Type 1 Diabetes

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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