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被动免疫抗甲状旁腺激素相关蛋白的作用:甲状旁腺激素相关蛋白是Walker癌肉瘤256大鼠模型中介导高钙血症的致病因素。

Effects of passive immunization against parathyroid hormone-related protein: PTHrP is the responsible factor in mediating hypercalcemia in the Walker carcinosarcoma 256 rat model.

作者信息

Schilling T, Blind E, Baier R, Sinn H P, Moallem E, Silver J, Ziegler R, Raue F

机构信息

Department of Internal Medicine I, University of Heidelberg, Germany.

出版信息

J Bone Miner Res. 1995 Jan;10(1):7-16. doi: 10.1002/jbmr.5650100105.

Abstract

The Walker carcinosarcoma (WCS) 256 is a well-characterized rat model of humoral hypercalcemia of malignancy (HHM). We addressed the question of whether parathyroid hormone-related protein (PTHrP) is the factor responsible for mediating HHM in this model. WCS 256 cells were subcutaneously implanted in female rats. We examined the plasma at days 0, 2, 4, 6, and 8. The midregional PTHrP measured by radioimmunoassay (RIA) and the plasma calcium increased significantly. Measuring PTHrP by a two-site immunoradiometric assay (IRMA) showed comparable results. There was a strong positive correlation between plasma calcium and midregional PTHrP (r = 0.85, p < 0.0001). A strong positive correlation between tumor weight and both midregional PTHrP (r = 0.83, p < 0.0001) and plasma calcium (r = 0.87, p < 0.0001) was also found. After surgical removal of the tumor at day 5, both plasma calcium and plasma PTHrP levels fell to within the normal range. Ip administration of native polyclonal antiserum against PTHrP(53-84) led to a significant decrease of plasma calcium. Extracted WCS 256 tumor showed 5-fold increased levels of midregional PTHrP compared with liver. Immunohistochemistry and Western blot were positive for PTHrP. RNA from the WCS 256 tumor was positive for PTHrP whereas liver tissue RNA was negative. WCS 256 cells grown in vitro also secreted PTHrP into the medium. We conclude that PTHrP is synthesized and secreted by WCS 256 and that PTHrP is the factor responsible for mediating hypercalcemia in the WCS 256 rat model.

摘要

沃克癌肉瘤(WCS)256是一种特征明确的恶性肿瘤体液性高钙血症(HHM)大鼠模型。我们探讨了甲状旁腺激素相关蛋白(PTHrP)是否是该模型中介导HHM的因子这一问题。将WCS 256细胞皮下植入雌性大鼠体内。我们在第0、2、4、6和8天检测血浆。通过放射免疫分析(RIA)测定的中部区域PTHrP和血浆钙显著升高。用双位点免疫放射分析(IRMA)测定PTHrP显示出类似结果。血浆钙与中部区域PTHrP之间存在强正相关(r = 0.85,p < 0.0001)。还发现肿瘤重量与中部区域PTHrP(r = 0.83,p < 0.0001)和血浆钙(r = 0.87,p < 0.0001)均呈强正相关。在第5天手术切除肿瘤后,血浆钙和血浆PTHrP水平均降至正常范围内。腹腔注射抗PTHrP(53 - 84)的天然多克隆抗血清导致血浆钙显著降低。提取的WCS 256肿瘤显示中部区域PTHrP水平比肝脏高5倍。免疫组织化学和蛋白质印迹法检测PTHrP呈阳性。WCS 2�6肿瘤的RNA对PTHrP呈阳性,而肝组织RNA为阴性。体外培养的WCS 256细胞也向培养基中分泌PTHrP。我们得出结论,PTHrP由WCS 256合成并分泌,且PTHrP是WCS 256大鼠模型中介导高钙血症的因子。

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