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CARD14 通过调控 MYC 对人类上皮细胞的影响是决定表皮稳态和疾病的关键因素。

Regulation of MYC by CARD14 in human epithelium is a determinant of epidermal homeostasis and disease.

机构信息

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA; Division of Asthma Research, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA; Division of Human Genetics, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.

Division of Asthma Research, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.

出版信息

Cell Rep. 2024 Aug 27;43(8):114589. doi: 10.1016/j.celrep.2024.114589. Epub 2024 Aug 6.

Abstract

Caspase recruitment domain family member 14 (CARD14) and its variants are associated with both atopic dermatitis (AD) and psoriasis, but their mechanistic impact on skin barrier homeostasis is largely unknown. CARD14 is known to signal via NF-κB; however, CARD14-NF-κB signaling does not fully explain the heterogeneity of CARD14-driven disease. Here, we describe a direct interaction between CARD14 and MYC and show that CARD14 signals through MYC in keratinocytes to coordinate skin barrier homeostasis. CARD14 directly binds MYC and influences barrier formation in an MYC-dependent fashion, and this mechanism is undermined by disease-associated CARD14 variants. These studies establish a paradigm that CARD14 activation regulates skin barrier function by two distinct mechanisms, including activating NF-κB to bolster the antimicrobial (chemical) barrier and stimulating MYC to bolster the physical barrier. Finally, we show that CARD14-dependent MYC signaling occurs in other epithelia, expanding the impact of our findings beyond the skin.

摘要

Caspase recruitment domain family member 14 (CARD14)及其变体与特应性皮炎 (AD) 和银屑病都有关,但它们对皮肤屏障稳态的机械影响在很大程度上尚不清楚。已知 CARD14 通过 NF-κB 信号传导;然而,CARD14-NF-κB 信号传导并不能完全解释由 CARD14 驱动的疾病的异质性。在这里,我们描述了 CARD14 与 MYC 之间的直接相互作用,并表明 CARD14 在角质形成细胞中通过 MYC 信号传导以协调皮肤屏障稳态。CARD14 直接结合 MYC,并以依赖 MYC 的方式影响屏障形成,而疾病相关的 CARD14 变体破坏了这种机制。这些研究确立了一个范例,即 CARD14 的激活通过两种不同的机制来调节皮肤屏障功能,包括激活 NF-κB 以增强抗菌(化学)屏障和刺激 MYC 以增强物理屏障。最后,我们表明 CARD14 依赖性 MYC 信号传导发生在其他上皮细胞中,将我们的发现的影响扩展到皮肤之外。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54c3/11469028/bf5caeebfbfa/nihms-2019535-f0002.jpg

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