Chen Hanqing, Li Tingting, Cai Ming, Huang Zhiqi, Gao Jianjun, Ding Hongping, Li Minmin, Guan Weiyu, Chen Jinpeng, Wang Wenran, Li Chunhong, Shi Jianwu
Basic Medical Research Centre, Medical School, Nantong University, Nantong, Jiangsu, China.
Department of Critical Care Medicine, Nantong Third People's Hospital, Nantong, Jiangsu, China.
Front Cell Dev Biol. 2025 Jan 8;12:1515524. doi: 10.3389/fcell.2024.1515524. eCollection 2024.
The normal development of the liver during human embryonic stages is critical for the functionality of the adult liver. Despite this, the essential genes, biological processes, and signal pathways that drive liver development in human embryos remain poorly understood.
In this study, liver samples were collected from human embryos at progressive developmental stages, ranging from 2-month-old to 7-month-old. Highly expressed genes and their associated enrichment processes at various developmental stages of the liver were identified through transcriptomic sequencing.
The findings indicated that genes associated with humoral immune responses and B-cell-mediated immunity were highly expressed during the early developmental stages. Concurrently, numerous genes related to vitamin response, brown adipocyte differentiation, T cell differentiation, hormone secretion, hemostasis, peptide hormone response, steroid metabolism, and hematopoietic regulation exhibited increased expression aligned with liver development. Our results suggest that the liver may possess multiple functions during embryonic stages, beyond serving hematopoietic roles. Moreover, this study elucidated the complex regulatory interactions among genes involved in lymphocyte differentiation, the regulation of hemopoiesis, and liver development. Consequently, the development of human embryonic liver necessitates the synergistic regulation of numerous genes. Notably, alongside conventionally recognized genes, numerous previously uncharacterized genes involved in liver development and function were also identified.
These findings establish a critical foundation for future research on liver development and diseases arising from fetal liver abnormalities.
人类胚胎期肝脏的正常发育对成年肝脏的功能至关重要。尽管如此,驱动人类胚胎肝脏发育的关键基因、生物学过程和信号通路仍知之甚少。
在本研究中,收集了2个月至7个月龄不同发育阶段的人类胚胎肝脏样本。通过转录组测序确定了肝脏各个发育阶段高表达的基因及其相关的富集过程。
研究结果表明,与体液免疫反应和B细胞介导的免疫相关的基因在早期发育阶段高表达。同时,许多与维生素反应、棕色脂肪细胞分化、T细胞分化、激素分泌、止血、肽激素反应、类固醇代谢和造血调节相关的基因随着肝脏发育表达增加。我们的结果表明,肝脏在胚胎期可能具有多种功能,而不仅仅是发挥造血作用。此外,本研究阐明了参与淋巴细胞分化、造血调节和肝脏发育的基因之间复杂的调控相互作用。因此,人类胚胎肝脏的发育需要众多基因的协同调控。值得注意的是,除了传统上公认的基因外,还鉴定出许多先前未表征的参与肝脏发育和功能的基因。
这些发现为未来肝脏发育以及由胎儿肝脏异常引起的疾病的研究奠定了关键基础。