Ayansola Hammed, Mayorga Edith J, Jin Younggeon
Department of Animal and Avian Sciences, University of Maryland, College Park, MD 20742, USA.
Department of Animal Sciences, Iowa State University, Ames, IA 50011, USA.
Biomedicines. 2024 Mar 17;12(3):668. doi: 10.3390/biomedicines12030668.
Intestinal epithelial cell activities during homeostasis and regeneration are well described, but their potential interactions with stromal cells remain unresolved. Exploring the functions of these heterogeneous intestinal mesenchymal stromal cells (iMSCs) remains challenging. This difficulty is due to the lack of specific markers for most functionally homogenous subpopulations. In recent years, however, novel clustering techniques such as single-cell RNA sequencing (scRNA-seq), fluorescence-activated cell sorting (FACS), confocal microscope, and computational remodeling of intestinal anatomy have helped identify and characterize some specific iMSC subsets. These methods help researchers learn more about the localization and functions of iMSC populations during intestinal morphogenic and homeostatic conditions. Consequently, it is imperative to understand the cellular pathways that regulate their activation and how they interact with surrounding cellular components, particularly during intestinal epithelial regeneration after mucosal injury. This review provides insights into the spatial distribution and functions of identified iMSC subtypes. It focuses on their involvement in intestinal morphogenesis, homeostasis, and regeneration. We reviewed related signaling mechanisms implicated during epithelial and subepithelial stromal cell crosstalk. Future research should focus on elucidating the molecular intermediates of these regulatory pathways to open a new frontier for potential therapeutic targets that can alleviate intestinal mucosa-related injuries.
肠道上皮细胞在稳态和再生过程中的活动已有充分描述,但其与基质细胞的潜在相互作用仍未明确。探索这些异质性肠道间充质基质细胞(iMSC)的功能仍然具有挑战性。造成这种困难的原因是大多数功能同质亚群缺乏特异性标志物。然而,近年来,诸如单细胞RNA测序(scRNA-seq)、荧光激活细胞分选(FACS)、共聚焦显微镜以及肠道解剖结构的计算重塑等新型聚类技术,有助于识别和表征一些特定的iMSC亚群。这些方法帮助研究人员更多地了解iMSC群体在肠道形态发生和稳态条件下的定位和功能。因此,了解调节其激活的细胞途径以及它们如何与周围细胞成分相互作用至关重要,尤其是在黏膜损伤后的肠道上皮再生过程中。本综述深入探讨了已识别的iMSC亚型的空间分布和功能。它重点关注了它们在肠道形态发生、稳态和再生中的作用。我们回顾了上皮细胞和上皮下基质细胞相互作用过程中涉及的相关信号机制。未来的研究应专注于阐明这些调节途径的分子中间体,为缓解肠道黏膜相关损伤的潜在治疗靶点开辟新的前沿领域。