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Lymphatic mapping of mice with systemic lymphoproliferative disorder: Usefulness as an inter-lymph node metastasis model of cancer

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单位: [1]Tohoku Univ, Dept Biomed Engn, Grad Sch Biomed Engn, Aoba Ku, Sendai, Miyagi 9808575, Japan [2]Huazhong Univ Sci & Technol, Tongji Hosp, Dept Oral & Maxillofacial Surg, Wuhan 430030, Hubei, Peoples R China [3]Tohoku Univ, Grad Sch Dent, Dept Oral Med & Surg, Aoba Ku, Sendai, Miyagi 9808575, Japan [4]Tohoku Univ, Dept Urol, Grad Sch Med, Aoba Ku, Sendai, Miyagi 980, Japan
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关键词: Lymphatic mapping Inter-lymph node vessels Lymph drainage-based drug delivery Cancer metastasis

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Preclinical models of lymph node (LN) metastasis are fundamental to the study and design of new techniques for the diagnosis and treatment of LN metastasis. However, the identification of LNs and lymphatic vessels (LVs) in mice is challenging with conventional imaging modalities, since the LN diameter in normal mice is 1-2 mm. Here, we describe MXH10/ Mo-lpr/lpr (MXH10/Mo/lpr) inbred mice, which develop systemic swelling of LNs up to 10 mm in diameter, allowing investigation of the topography of LNs and LVs. Using a gross anatomy dissection approach, we identified 22 different LNs situated in the head and neck, limbs, thoracic and abdominal regions. Furthermore, four peripheral inter-LN vessels were found: from the subiliac LN (SiLN) to the proper axillary LN (PALN); from the parotid LN to the caudal deep cervical LN; and from the popliteal LN to both the sciatic LN and the SiLN. Metastasis to the PALN via LVs was induced by inoculating FM3A/Luc mouse mammary carcinoma cells into the SiLN. Our results demonstrate that the MXH10/Mo/lpr mouse strain is an excellent model in which to investigate lymphatic drainage and inter-LN metastasis of cancer. This paper unveils the anatomy of murine lymphatics to give new insights into the investigation of inter-LN metastasis of cancer, especially the mechanisms involved in the trafficking of cancer cells through inter-LN vessels. The results provide data that may prove very useful in the quest to develop better lymph drainage-based drug delivery systems. (C) 2013 Elsevier B.V. All rights reserved.

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出版当年[2012]版:
大类 | 3 区 医学
小类 | 4 区 生化研究方法 4 区 免疫学
最新[2025]版:
大类 | 4 区 医学
小类 | 4 区 生化研究方法 4 区 免疫学
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出版当年[2011]版:
Q3 BIOCHEMICAL RESEARCH METHODS Q3 IMMUNOLOGY
最新[2023]版:
Q4 BIOCHEMICAL RESEARCH METHODS Q4 IMMUNOLOGY

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第一作者单位: [1]Tohoku Univ, Dept Biomed Engn, Grad Sch Biomed Engn, Aoba Ku, Sendai, Miyagi 9808575, Japan [2]Huazhong Univ Sci & Technol, Tongji Hosp, Dept Oral & Maxillofacial Surg, Wuhan 430030, Hubei, Peoples R China
通讯作者:
通讯机构: [1]Tohoku Univ, Dept Biomed Engn, Grad Sch Biomed Engn, Aoba Ku, Sendai, Miyagi 9808575, Japan [*1]Tohoku Univ, Mol Delivery Syst Lab, Dept Biomed Engn, Grad Sch Biomed Engn,Aoba Ward, 4-1 Seiryo, Sendai, Miyagi 9808575, Japan
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