Michael Helmrath · Guanylate cyclase 2C agonism corrects CFTR mutants
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Article1 min read·Published Oct 2017Older

Guanylate cyclase 2C agonism corrects CFTR mutants

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Article · Oct 2017 · 1 min read

In brief

In brief

This study identifies guanylate cyclase 2C (GCC) as a novel therapeutic target for correcting CFTR mutations in cystic fibrosis intestinal disease. GCC activation functionally rescues common CFTR mutants including F508del in patient-derived intestinal models, offering a potential treatment for CF-associated constipation and intestinal fluid deficits.

Written by the GCMD Library team from the article.

Michael Helmrath

Cystic fibrosis (CF) is a genetic disorder in which epithelium-generated fluid flow from the lung, intestine, and pancreas is impaired due to mutations disrupting CF transmembrane conductance regulator (CFTR) channel function. CF manifestations of the pancreas and lung are present in the vast majority of CF patients, and 15% of CF infants are born with obstructed gut or meconium ileus. However, constipation is a significantly underreported outcome of CF disease, affecting 47% of the CF patients, and management becomes critical in the wake of increasing life span of CF patients. In this study, we unraveled a potentially novel molecular role of a membrane-bound cyclic guanosine monophosphate-synthesizing (cGMP-synthesizing) intestinal enzyme, guanylate cyclase 2C (GCC) that could be targeted to ameliorate CF-associated intestinal fluid deficit. We demonstrated that GCC agonism results in functional rescue of murine F508del/F508del and R117H/R117H Cftr and CFTR mutants in CF patient-derived intestinal spheres. GCC coexpression and activation facilitated processing and ER exit of F508del CFTR and presented a potentially novel rescue modality in the intestine, similar to the CF corrector VX-809. Our findings identify GCC as a biological CFTR corrector and potentiator in the intestine.

Statements in this article

  1. Cystic fibrosis is a genetic disorder in which epithelium-generated fluid flow from the lung, intestine, and pancreas is impaired due to mutations disrupting CFTR channel function.

    Established
  2. CF manifestations of the pancreas and lung are present in the vast majority of CF patients.

    Established
  3. 15% of CF infants are born with obstructed gut or meconium ileus.

    Research
  4. Constipation affects 47% of CF patients.

    Research
  5. GCC agonism results in functional rescue of murine F508del/F508del and R117H/R117H Cftr mutants.

    Research
  6. GCC agonism results in functional rescue of CFTR mutants in CF patient-derived intestinal spheres.

    Research
  7. GCC coexpression and activation facilitated processing and ER exit of F508del CFTR.

    Research
  8. GCC presents a potentially novel rescue modality in the intestine, similar to the CF corrector VX-809.

    Research

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