Nash Michael J, Dobrinskikh Evgenia, Al-Juboori Saif I, Janssen Rachel C, Fernandes Jolyn, Argabright Amy, D'Alessandro Angelo, Kirigiti Melissa A, Kievit Paul, Aagaard Kjersti M, McCurdy Carrie E, Gannon Maureen, Jones Kenneth L, Li Tiangang, Friedman Jacob E, Wesolowski Stephanie R
Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Harold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
Liver Int. 2025 Feb;45(2):e16236. doi: 10.1111/liv.16236.
Maternal obesity increases the risk of the paediatric form of metabolic dysfunction-associated steatotic liver disease (MASLD), affecting up to 30% of youth, but the developmental origins remain poorly understood.
Using a Japanese macaque model, we investigated the impact of maternal Western-style diet (mWSD) or chow diet followed by postweaning WSD (pwWSD) or chow diet focusing on bile acid (BA) homeostasis and hepatic fibrosis in livers from third-trimester fetuses and 3-year-old juvenile offspring.
Juveniles exposed to mWSD had increased hepatic collagen I/III content and stellate cell activation in portal regions. mWSD increased transcriptional signatures of FXR activation, while pwWSD impaired FXR pathway genes and increased liver BA content. Both mWSD and pwWSD increased serum BA concentrations. Notably, mWSD-exposed juvenile offspring had increased periportal CK19 expression and cholangiocyte gene expression supporting proliferation compared with maternal chow-exposed offspring. Fetuses exposed to mWSD had increased CK19 expression and hepatic BAs which correlated positively with periportal collagen deposition and negatively with markers of fetal oxygenation. In juvenile offspring, increased serum BAs correlated positively with hepatic oxidative stress and portal fibrosis without elevated liver enzymes.
mWSD is associated with hallmarks of paediatric MASLD including portal bile ductular reaction, portal fibrosis and dysregulated BA homeostasis. These conditions begin in utero and persist in juvenile offspring regardless of their postweaning diet. These findings implicate changes in BA metabolism that may drive developmental programming of MASLD in juvenile offspring beginning in utero.
母亲肥胖会增加儿童期代谢功能障碍相关脂肪性肝病(MASLD)的发病风险,影响高达30%的青少年,但疾病的发育起源仍知之甚少。
我们使用日本猕猴模型,研究母亲西式饮食(mWSD)或普通饮食后断奶后西式饮食(pwWSD)或普通饮食对孕晚期胎儿和3岁幼年后代肝脏中胆汁酸(BA)稳态和肝纤维化的影响。
暴露于mWSD的幼年猕猴门静脉区域肝I/III型胶原含量增加,星状细胞活化。mWSD增加了FXR激活的转录特征,而pwWSD损害了FXR通路基因并增加了肝脏BA含量。mWSD和pwWSD均增加了血清BA浓度。值得注意的是,与母亲食用普通饮食的后代相比,暴露于mWSD的幼年后代门静脉周围CK19表达增加,胆管细胞基因表达支持增殖。暴露于mWSD的胎儿CK19表达增加,肝脏BA增加,这与门静脉周围胶原沉积呈正相关,与胎儿氧合标记物呈负相关。在幼年后代中,血清BA升高与肝脏氧化应激和门静脉纤维化呈正相关,而肝酶未升高。
mWSD与儿童MASLD的特征有关,包括门静脉胆管反应、门静脉纤维化和BA稳态失调。这些情况始于子宫内,并在幼年后代中持续存在,无论其断奶后的饮食如何。这些发现表明BA代谢的变化可能驱动子宫内开始的幼年后代MASLD的发育编程。