利用神经元特异性β -微管蛋白III观察两种柽柳猴舌鼻器官的个体发生。

Timothy D Smith, John C Dennis, Kunwar P Bhatnagar, Christopher J Bonar, Annie M Burrows, Edward E Morrison
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引用次数: 8

摘要

鸡毛猴(绢毛猴、狨猴)在犁鼻器官(VNO)上存在极端差异,包括出生时神经上皮和犁鼻管(VND)通畅的个体发生差异。这些差异使得叶酸中VNO成熟的时间和程度存在争议,但没有研究使用神经元特异性免疫组织化学标记来解决这个问题。本研究比较了两种狨猴(Leontopithecus rosalia和Saguinus geoffroyi)在围产期VND通畅程度不同的VNO上皮细胞表达神经元特异性β -微管蛋白III (BT)免疫反应性的数量、VNO长度和VNO横截面积。新生狐猴、成年狨猴和丛林婴儿也被检查,以与先前显示具有相对大量VNO神经上皮和未专利vnd的物种进行比较。每个标本的头部在冠状面连续切片。根据已知的VNO的头侧开始/停止点,选择未染色的切片在每个标本的三个百分位数(25、50、75)进行BT协议和面积测量。每个切片被拍照和放大,用于细胞计数和测量横截面上皮面积。在每个标本中,按每个百分位数计数VNO中BT(+)细胞的数量,并以每mm的数量表示(2)。结果表明,狐猴出生时VNO中BT(+)细胞密度较高,而绢毛猴的VNO差异较大。在融合了VND的新生儿中,geoffroys的vno中BT(+)细胞很少或没有,但在出生后1个月和2个月,当VND形成时,BT(+)细胞数量增加。在出生时具有专利VNDs的物种中,新生儿rosalia的BT(+)细胞数量比S. geoffroyi更密集,尽管在新生儿狐猴或成年狨猴和丛林婴儿中所见的程度不同。这些结果表明,BT免疫组织化学是研究亚成年灵长类动物VNOs的一种有用的比较方法。由于非感觉VNO上皮的数量在物种之间存在很大差异,因此上皮面积的测量可能会产生误导,而BT(+)细胞计数似乎是比较灵长类动物受体神经元数量的最佳定量方法。这表明,在所有亚成虫阶段,rosalia中较大的BT(+)细胞群表明,与geoffroroyi相比,rosalia的神经上皮成熟得更早。进一步的研究应该考虑这是否可能与相对较短的亚成虫个体发育和较早的成虫行为有关。
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Ontogenetic observations on the vomeronasal organ in two species of tamarins using neuron-specific beta-tubulin III.

Callitrichid primates (tamarins, marmosets) have extreme variation in the vomeronasal organ (VNO), including ontogenetic differences in the neuroepithelium and vomeronasal duct (VND) patency at birth. Such differences render the timing and extent of VNO maturation debatable in callitrichids, but no studies have used neuron-specific immunohistochemical markers to address this question. The present study compared the number of VNO epithelial cells that express immunoreactivity to neuron-specific beta-tubulin III (BT), VNO length, and VNO cross-sectional area between two species of tamarins (Leontopithecus rosalia and Saguinus geoffroyi) that differed in perinatal VND patency. Neonatal lemurs and adult marmosets and bushbabies were also examined for a comparison to species previously shown to have a relatively large amount of VNO neuroepithelium and patent VNDs. The head of each specimen was serially sectioned in the coronal plane. Based on known rostrocaudal start/stop points of the VNO, selected unstained sections were used for BT protocols and area measurement at three percentiles (25th, 50th, 75th) in each specimen. Each section was photographed and enlarged for cell counts and measurement of cross-sectional epithelial area. In each specimen, the number of BT(+) cells in the VNO was counted at each percentile and expressed as a number per mm(2). Results indicated that lemur VNOs had a dense population of BT(+) cells at birth, but the VNO was more varied in the tamarin species. S. geoffroyi had few or no BT(+) cells in VNOs of neonates, which had fused VNDs, but had an increased BT(+) population by 1 and 2 months postnatal age, when the VND was patent. Of the species with patent VNDs at birth, neonatal L. rosalia had a denser population of BT(+) cells compared to S. geoffroyi, though not to the degree seen in neonatal lemurs or adult marmosets and bushbabies. These findings show that BT immunohistochemistry is a useful comparative method for the study of VNOs in subadult primates. Since the quantity of nonsensory VNO epithelium varies substantially between species, epithelial area measurements may be misleading, and BT(+) cell counts appeared to be the best quantitative method for comparing receptor neuron numbers among primates. It is suggested that the greater BT(+) cell population in L. rosalia at all subadult stages examined reveals an earlier maturation of the neuroepithelium compared to S. geoffroyi. Further investigation should consider whether this may relate to a comparatively brief subadult ontogeny and early onset of adult behaviors in L. rosalia compared to other tamarins studied to date.

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