Using β-Cell Growth Factors to Enhance Human Pancreatic Islet Transplantation*
Author(s) -
Adolfo GarcíaOcaña,
Rupangi C. Vasavada,
Karen K. Takane,
Ana Cebrián,
Juan Carlos LopezTalavera,
Andrew F. Stewart
Publication year - 2001
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jcem.86.3.7315
Subject(s) - islet , transplantation , pancreatic islets , diabetes mellitus , pancreatic function , optimism , medicine , biology , endocrinology , pancreas , psychology , social psychology
This is a particularly exciting time in the field of pancreatic islet growth, development, and survival. The recent publication of a study demonstrating that human pancreatic islet transplantation is both technically and immunologically feasible has highlighted the need for large supplies of pancreatic islets or pancreatic beta cells for larger-scale islet transplantation in patients with diabetes. This, together with a rapid expansion in the past several years of the understanding of mechanisms of islet growth, development, and survival, has accelerated and invigorated efforts to therapeutically harness the cellular mechanisms responsible for pancreatic beta-cell proliferation, survival, and development and to take advantage of this new knowledge to enhance the availability, survival, and function of pancreatic beta cells in human islet transplantation for diabetes mellitus. Here, we briefly review the confluence of events that have provided optimism and energy to the islet transplant field, and we focus on peptide growth factors that eventually may be deployed in the effort to augment islet mass and function in patients with diabetes.
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