雌性 Alms1 基因缺陷小鼠会出现成人阿尔斯特罗姆综合征心肌病的超声心动图特征,但不会出现婴儿阿尔斯特罗姆综合征心肌病的超声心动图特征。

IF 4 3区 医学 Q2 CELL BIOLOGY
Disease Models & Mechanisms Pub Date : 2024-06-01 Epub Date: 2024-06-28 DOI:10.1242/dmm.050561
Eleanor J McKay, Ineke Luijten, Sophie Broadway-Stringer, Adrian Thomson, Xiong Weng, Katya Gehmlich, Gillian A Gray, Robert K Semple
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引用次数: 0

摘要

阿尔斯特姆综合征(AS)是由双偶ALMS1基因突变引起的一种多系统疾病,其特征是心脏并发症导致的严重早期发病率和死亡率。这些并发症是双相的,包括婴儿期扩张型心肌病和独特的成人发病型心肌病,但人们对其了解甚少。我们通过超声心动图评估了 Alms1 基因敲除小鼠的心脏功能。在出生后第 15 天(P15)和 8 周时,雌雄 Alms1 基因敲除小鼠的心脏功能均无改变。23 周时,雌性而非雄性基因敲除小鼠的左心房面积增大,等容舒张时间缩短,这与早期限制性心肌病以及射血分数降低一致。23 周大的 Alms1 基因全面敲除雌性小鼠的心肌未出现组织学或转录变化。在心脏成纤维细胞和一小部分心肌细胞中进行 Pdgfrα-Cre 驱动的 Alms1 基因缺失的雌性小鼠在 23 周时并没有再现全基因敲除的表型。总之,成年雌性 Alms1 基因缺陷小鼠(而非雄性)显示出心脏功能障碍的超声心动图证据,与强直性脊柱炎的心肌病相一致。性双态性的解释仍不清楚,但可能涉及两性之间的代谢或内分泌差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Female Alms1-deficient mice develop echocardiographic features of adult but not infantile Alström syndrome cardiomyopathy.

Alström syndrome (AS), a multisystem disorder caused by biallelic ALMS1 mutations, features major early morbidity and mortality due to cardiac complications. The latter are biphasic, including infantile dilated cardiomyopathy and distinct adult-onset cardiomyopathy, and poorly understood. We assessed cardiac function of Alms1 knockout (KO) mice by echocardiography. Cardiac function was unaltered in Alms1 global KO mice of both sexes at postnatal day 15 (P15) and 8 weeks. At 23 weeks, female - but not male - KO mice showed increased left atrial area and decreased isovolumic relaxation time, consistent with early restrictive cardiomyopathy, as well as reduced ejection fraction. No histological or transcriptional changes were seen in myocardium of 23-week-old female Alms1 global KO mice. Female mice with Pdgfra-Cre-driven Alms1 deletion in cardiac fibroblasts and in a small proportion of cardiomyocytes did not recapitulate the phenotype of global KO at 23 weeks. In conclusion, only female Alms1-deficient adult mice show echocardiographic evidence of cardiac dysfunction, consistent with the cardiomyopathy of AS. The explanation for sexual dimorphism remains unclear but might involve metabolic or endocrine differences between sexes.

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来源期刊
Disease Models & Mechanisms
Disease Models & Mechanisms 医学-病理学
CiteScore
6.60
自引率
7.00%
发文量
203
审稿时长
6-12 weeks
期刊介绍: Disease Models & Mechanisms (DMM) is an online Open Access journal focusing on the use of model systems to better understand, diagnose and treat human disease.
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