Krassioukov A V, Bygrave M A, Puckett W R, Bunge R P, Rogers K A
The John P. Robarts Research Institute and The Department of Physiology of the University of Western Ontario, London, Canada.
J Auton Nerv Syst. 1998 May 28;70(1-2):123-8. doi: 10.1016/s0165-1838(98)00042-3.
The retrograde tracer 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI) was used to label sympathetic preganglionic neurons (SPN) and motoneurons (MN) in postmortem human spinal cord. Seven months after microinjection of DiI into the ventral part of spinal thoracic segments T4 and T8, DiI-labelled neurons were identified and analyzed. Cryostat sections of spinal cord were prepared for light microscopy, while vibratome sections were analyzed using confocal microscopy. The majority of retrogradely labelled SPNs were located within the intermediolateral nucleus, with a few labelled dendrites having a mediolateral orientation. SPNs were also located within the nucleus intercalatus, around the central canal and in the lateral funiculus. Cell bodies of retrogradely labelled IML neurons were oval, kite- or spindle-shaped. The soma area of SPNs in T4 was approximately 422.9 +/- 20.9 microm2 with a median diameter of 14 +/- 0.6 microm. MNs in the ventral horn were round or oval in shape and often appeared with a few labelled neurites. The soma area of the MNs in T4 was approximately 842.3 +/- 35.1 microm2, with a median diameter of 18.3 +/- 0.1 microm. The mean values for MN soma area and diameter measurements were significantly greater compared to SPNs. However, no difference was observed between MNs in different segments or between SPNs in the same segments. No retrogradely labelled cells were observed within the dorsal horn. These findings indicate that DiI is a useful method for studying fixed human central nervous system tissue.
逆行示踪剂1,1'-二辛基-3,3,3',3'-四甲基吲哚羰花青高氯酸盐(DiI)用于标记死后人类脊髓中的交感神经节前神经元(SPN)和运动神经元(MN)。在将DiI微量注射到胸段脊髓T4和T8腹侧部分七个月后,对DiI标记的神经元进行识别和分析。制备脊髓冰冻切片用于光学显微镜检查,而振动切片则使用共聚焦显微镜进行分析。大多数逆行标记的SPN位于中间外侧核内,少数标记的树突具有中外侧方向。SPN也位于中间插入核内、中央管周围和外侧索内。逆行标记的中间外侧柱神经元的细胞体呈椭圆形、风筝形或纺锤形。T4中SPN的胞体面积约为422.9±20.9平方微米,中位直径为14±0.6微米。腹角中的MN呈圆形或椭圆形,通常有一些标记的神经突。T4中MN的胞体面积约为842.3±35.1平方微米,中位直径为18.3±0.1微米。与SPN相比,MN胞体面积和直径测量的平均值明显更大。然而,不同节段的MN之间或同一节段的SPN之间未观察到差异。在背角内未观察到逆行标记的细胞。这些发现表明,DiI是研究固定人类中枢神经系统组织的一种有用方法。