This study was conducted in accordance with the protocols reviewed and approved by the Institutional Animal Care and Use Committee at Massachusetts General Hospital (Protocol #2009N000239). All methods were carried out in accordance with relevant guidelines and regulations. The reporting in the manuscript follows the recommendations in the ARRIVE guidelines.
Wnt1::Cre mice (Stock #003829 and Stock #009107), R26R-tdT reporter mice (Stock #007914), and R26R-ChR2tdT reporter mice (Stock #012567) were purchased from Jackson Laboratory (Bar Harbor, ME, USA). Wnt1::Cre mice were crossed with R26R-tdT and R26R-ChR2tdT reporter mice to generate Wnt1::Cre;R26-tdT (annotated as Wnt1-tdT) and Wnt1::Cre;R26-ChR2tdT (annotated as Wnt1-ChR2) mice, respectively.
We also generated Plp1-GFP;Wnt1-tdT mice [22 (link)] in which enteric glial cells express GFP and neural crest-derived ENS expresses tdTomato by crossing Plp1GFP;Wnt1::Cre mice with R26R-tdT mice. Plp1GFP mice [23 (link)] were kindly gifted by Dr. Wendy Macklin, University of Colorado, Denver. Heterozygote nNOS mice (Stock #002986) were purchased from Jackson Laboratory and bred to obtain homozygote nNOS knockout mice (nNOS−/−).
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