Pluripotent Stem Cell Models of Shwachman-Diamond Syndrome Reveal a Common Mechanism for Pancreatic and Hematopoietic Dysfunction
Shwachman-Diamond syndrome (SDS), a rare autosomal-recessive disorder characterized by exocrine pancreatic insufficiency and hematopoietic dysfunction, is caused by mutations in the Shwachman-Bodian-Diamond syndrome (SBDS) gene. We created human pluripotent stem cell models of SDS through knockdown...
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Veröffentlicht in: | Cell stem cell 2013-06, Vol.12 (6), p.727-736 |
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Sprache: | eng |
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Zusammenfassung: | Shwachman-Diamond syndrome (SDS), a rare autosomal-recessive disorder characterized by exocrine pancreatic insufficiency and hematopoietic dysfunction, is caused by mutations in the Shwachman-Bodian-Diamond syndrome (SBDS) gene. We created human pluripotent stem cell models of SDS through knockdown of SBDS in human embryonic stem cells (hESCs) and generation of induced pluripotent stem cell (iPSC) lines from two patients with SDS. SBDS-deficient hESCs and iPSCs manifest deficits in exocrine pancreatic and hematopoietic differentiation in vitro, enhanced apoptosis, and elevated protease levels in culture supernatants, which could be reversed by restoring SBDS protein expression through transgene rescue or by supplementing culture media with protease inhibitors. Protease-mediated autodigestion provides a mechanistic link between the pancreatic and hematopoietic phenotypes in SDS, highlighting the utility of hESCs and iPSCs in obtaining novel insights into human disease.
•We generated human pluripotent stem cell models of SDS in hESCs and iPSCs•Increased apoptosis was present in pancreatic and hematopoietic lineages•Protease activity was elevated in pancreatic and hematopoietic cultures•Protease inhibitors reversed differentiation defects and apoptosis
hESC and iPSC models of Shwachman-Diamond syndrome reveal elevated protease activity as a common underlying mechanism for dysfunction in pancreatic and hematopoietic lineages. |
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ISSN: | 1934-5909 1875-9777 |
DOI: | 10.1016/j.stem.2013.04.002 |