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Merck
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  • Δ9-Tetrahydrocannabinol inhibits Hedgehog-dependent patterning during development.

Δ9-Tetrahydrocannabinol inhibits Hedgehog-dependent patterning during development.

Development (Cambridge, England) (2021-10-06)
Hsiao-Fan Lo, Mingi Hong, Henrietta Szutorisz, Yasmin L Hurd, Robert S Krauss
摘要

Many developmental disorders are thought to arise from an interaction between genetic and environmental risk factors. The Hedgehog (HH) signaling pathway regulates myriad developmental processes, and pathway inhibition is associated with birth defects, including holoprosencephaly (HPE). Cannabinoids are HH pathway inhibitors, but little is known of their effects on HH-dependent processes in mammalian embryos, and their mechanism of action is unclear. We report that the psychoactive cannabinoid Δ9-tetrahydrocannabinol (THC) induces two hallmark HH loss-of-function phenotypes (HPE and ventral neural tube patterning defects) in Cdon mutant mice, which have a subthreshold deficit in HH signaling. THC therefore acts as a 'conditional teratogen', dependent on a complementary but insufficient genetic insult. In vitro findings indicate that THC is a direct inhibitor of the essential HH signal transducer smoothened. The canonical THC receptor, cannabinoid receptor-type 1, is not required for THC to inhibit HH signaling. Cannabis consumption during pregnancy may contribute to a combination of risk factors underlying specific developmental disorders. These findings therefore have significant public health relevance.

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Roche
抗地高辛-AP,Fab片段, from sheep
Sigma-Aldrich
抗乙酰化微管蛋白抗体,小鼠单克隆 小鼠抗, clone 6-11B-1, purified from hybridoma cell culture
Sigma-Aldrich
抗-寡糖-2 抗体, Chemicon®, from rabbit
Roche
胶原, from rat tail tendon
Sigma-Aldrich
平滑激动剂,SAG, A cell-permeable Smoothened Agonist, SAG, CAS 364590-63-6, modulates the coupling of Smo with its downstream effector by interacting with the Smo heptahelical domain (KD = 59 nM).
Sigma-Aldrich
单克隆抗 β-微管蛋白 III 小鼠抗, clone SDL.3D10, ascites fluid
Sigma-Aldrich
SANT-1, A potent, cell-permeable antagonist of the Shh signaling pathway by binding directly to Smoothened, a distant relative of G protein-coupled receptors.