Nanda Reetuparna, Bota Mihail, Jayakumar Jaikishan, S Suresh, Lata S, Kumar E Harish, Srinivasan Chitra, Vasudevan Sudha, Jayaraman Kumutha, Sivaprakasam Mohanasankar, Verma Richa
Sudha Gopalakrishnan Brain Centre, Indian Institute of Technology Madras, Chennai, India.
Center for Computational Brain Research, Indian Institute of Technology Madras, Chennai, India.
Front Neuroanat. 2025 Jan 6;18:1502778. doi: 10.3389/fnana.2024.1502778. eCollection 2024.
The inferior colliculus (IC) is an important midbrain station of the auditory pathway, as well as an important hub of multisensory integration. The adult mammalian IC can be subdivided into three nuclei, with distinct cyto- and myeloarchitectonical profiles and distinct calcium binding proteins expression patterns. Despite several studies about its structural and functional development, the knowledge about the human fetal IC is rather limited. In this paper we first systematically describe the histological development of the human fetal IC and its subparts in five stages of the second trimester of pregnancy: 15 gestation weeks (GW), 18 GW, 21 GW, 24 GW, and 27 GW. We 3D reconstruct and calculate the volumetric growth of IC from one stage to another, which increases from 12.85 mm at 15 GW to 34.27 mm at 27 GW in the left hemisphere. The volumetric changes in the IC were further evaluated at the cellular level using serial Nissl-stained sections, as well as glial fibrillary acidic proteins (GFAP) and calretinin immunohistochemistry. We identify stellate-like and round neurons in the central nucleus of the IC (CNIC) at 24 GW and 27 GW, comparable to the adult human IC. Novel in this study, we investigate the differential calretinin expression patterns in the IC subparts, from 15 GW to 27 GW. CR labeling is identified mainly in the cortical IC rather than in the central nucleus. Furthermore, using GFAP, we describe the radial glial fibers patterns in IC, which are dominant at 18 GW and gradually taper off at later developmental stages. Finally, we describe the development of astroglia in each of the five developmental stages. All these results indicate that the human fetal IC development and cellular maturation occur in two major stages during the second trimester.
下丘(IC)是听觉通路中一个重要的中脑站点,也是多感官整合的重要枢纽。成年哺乳动物的IC可细分为三个核,具有不同的细胞和髓鞘构筑特征以及不同的钙结合蛋白表达模式。尽管有几项关于其结构和功能发育的研究,但关于人类胎儿IC的知识相当有限。在本文中,我们首先系统地描述了妊娠中期五个阶段(妊娠15周(GW)、18 GW、21 GW、24 GW和27 GW)人类胎儿IC及其各部分的组织学发育。我们对IC从一个阶段到另一个阶段进行三维重建并计算其体积增长,左半球的IC体积从15 GW时的12.85立方毫米增加到27 GW时的34.27立方毫米。使用连续的尼氏染色切片以及胶质纤维酸性蛋白(GFAP)和钙视网膜蛋白免疫组织化学在细胞水平上进一步评估IC的体积变化。我们在24 GW和27 GW时在IC的中央核(CNIC)中鉴定出星状样和圆形神经元,这与成年人类IC相似。本研究的新颖之处在于,我们研究了从15 GW到27 GW时IC各部分中钙视网膜蛋白的差异表达模式。CR标记主要在皮质IC中而非中央核中被鉴定出来。此外,使用GFAP,我们描述了IC中的放射状胶质纤维模式,其在18 GW时占主导地位,并在后期发育阶段逐渐减少。最后,我们描述了五个发育阶段中每个阶段星形胶质细胞的发育情况。所有这些结果表明,人类胎儿IC的发育和细胞成熟在妊娠中期的两个主要阶段发生。