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在接受垂体移植的小鼠中,Fr-MLV感染诱发的是红白血病而非淋巴细胞白血病。

Fr-MLV infection induces erythroleukaemia instead of lymphoid leukaemia in mice given pituitary grafts.

作者信息

Fontanini G, Basolo F, Garzelli C, Squartini F, Toniolo A

机构信息

Institute of Pathological Anatomy and Histology, University of Pisa, Italy.

出版信息

Br J Cancer. 1990 Jun;61(6):841-5. doi: 10.1038/bjc.1990.188.

Abstract

Here we report that the slow-transforming helper component of Friend murine leukaemia virus (Fr-MLV), which produces lymphoid leukaemias in normal mice, induces erythroleukaemia in mice given syngeneic pituitary grafts (SPG). Newborn mice were infected with Fr-MLV and, at one month of age, were transplanted with two pituitary glands under the kidney capsule. Sham-operated infected mice and uninfected transplanted mice served as controls. SPG selectively reduced the mean survival times of infected mice. Histopathology showed that, while most infected non-transplanted mice developed lymphoid leukaemias, virtually all Fr-MLF-infected mice given SPG developed erythroleukaemias. Experiments in vitro showed that Fr-MLV infection markedly depressed concanavalin A induced DNA synthesis in cells from spleen, thymus and lymph nodes. Addition of prolactin or growth hormone further suppressed lectin-induced mitogenesis of lymphoid cells from infected mice, but failed to influence the response of uninfected controls. These experiments indicate that, in mice, pituitary hormones modulate the development and the histological features of Fr-MLV induced leukaemias, and suggest that endocrine-immunological interactions play a role in retrovirus induced tumorigenesis.

摘要

在此我们报告,弗瑞德氏鼠白血病病毒(Fr-MLV)的慢转化辅助成分,能在正常小鼠中引发淋巴白血病,而在接受同基因垂体移植(SPG)的小鼠中则诱发红白血病。新生小鼠感染Fr-MLV,在1月龄时于肾被膜下移植两个垂体。假手术感染小鼠和未感染移植小鼠作为对照。SPG选择性缩短了感染小鼠的平均存活时间。组织病理学显示,大多数感染但未移植的小鼠发生淋巴白血病,而几乎所有接受SPG的Fr-MLV感染小鼠都发生了红白血病。体外实验表明,Fr-MLV感染显著抑制了来自脾脏、胸腺和淋巴结细胞中伴刀豆球蛋白A诱导的DNA合成。添加催乳素或生长激素进一步抑制了感染小鼠淋巴样细胞的凝集素诱导的有丝分裂,但对未感染对照的反应没有影响。这些实验表明,在小鼠中,垂体激素调节Fr-MLV诱导的白血病的发展和组织学特征,并提示内分泌-免疫相互作用在逆转录病毒诱导的肿瘤发生中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eef/1971688/b566d7fc53d2/brjcancer00226-0057-a.jpg

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