Laboratorio de Patología Diagnóstica e Inmunohistoquímica, Centro de Investigación y Diagnóstico en Patología, Departamento de Microbiología y Patología, CUCS, Universidad de Guadalajara, Guadalajara 44340, Mexico.
Doctorado en Ciencias en Biología Molecular en Medicina, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara 44340, Mexico.
Cells. 2023 Jun 27;12(13):1733. doi: 10.3390/cells12131733.
During embryonic and fetal development, the cerebellum undergoes several histological changes that require a specific microenvironment. Pleiotrophin (PTN) has been related to cerebral and cerebellar cortex ontogenesis in different species. PTN signaling includes PTPRZ1, ALK, and NRP-1 receptors, which are implicated in cell differentiation, migration, and proliferation. However, its involvement in human cerebellar development has not been described so far. Therefore, we investigated whether PTN and its receptors were expressed in the human cerebellar cortex during fetal and early neonatal development. The expression profile of PTN and its receptors was analyzed using an immunohistochemical method. PTN, PTPRZ1, and NRP-1 were expressed from week 17 to the postnatal stage, with variable expression among granule cell precursors, glial cells, and Purkinje cells. ALK was only expressed during week 31. These results suggest that, in the fetal and neonatal human cerebellum, PTN is involved in cell communication through granule cell precursors, Bergmann glia, and Purkinje cells via PTPRZ1, NRP-1, and ALK signaling. This communication could be involved in cell proliferation and cellular migration. Overall, the present study represents the first characterization of PTN, PTPRZ1, ALK, and NRP-1 expression in human tissues, suggesting their involvement in cerebellar cortex development.
在胚胎和胎儿发育过程中,小脑经历了几次组织学变化,需要特定的微环境。多效蛋白(PTN)与不同物种的大脑和小脑皮质发生有关。PTN 信号包括 PTPRZ1、ALK 和 NRP-1 受体,这些受体参与细胞分化、迁移和增殖。然而,其在人类小脑发育中的作用尚未被描述。因此,我们研究了 PTN 及其受体是否在人类胎儿和新生儿小脑皮质发育过程中表达。使用免疫组织化学方法分析了 PTN 及其受体的表达谱。PTN、PTPRZ1 和 NRP-1 的表达从第 17 周持续到出生后阶段,在颗粒细胞前体、神经胶质细胞和浦肯野细胞之间的表达存在差异。ALK 仅在第 31 周表达。这些结果表明,在胎儿和新生儿人类小脑,PTN 通过颗粒细胞前体、Bergmann 胶质细胞和浦肯野细胞通过 PTPRZ1、NRP-1 和 ALK 信号参与细胞通讯。这种通讯可能涉及细胞增殖和细胞迁移。总的来说,本研究首次描述了 PTN、PTPRZ1、ALK 和 NRP-1 在人类组织中的表达,表明它们参与了小脑皮质的发育。