Phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes

被引:39
作者
Botting, Rachel A. [1 ,2 ]
Bertram, Kirstie M. [1 ,2 ]
Baharlou, Heeva [1 ,2 ]
Sandgren, Kerrie J. [1 ]
Fletcher, James [3 ]
Rhodes, Jake W. [1 ,2 ]
Rana, Hafsa [1 ,2 ]
Plasto, Toby M. [1 ,2 ]
Wang, Xin Maggie [1 ]
Lim, Jake J. K.
Barnouti, Laith [4 ]
Kohout, Mark P. [4 ]
Papadopoulos, Tim [5 ]
Merten, Steve [6 ]
Olbourne, Norman
Cunningham, Anthony L. [1 ,2 ]
Haniffa, Muzlifah [3 ,7 ]
Harman, Andrew N. [1 ,2 ]
机构
[1] Westmead Inst Med Res, Ctr Virus Res, 176 Hawkesbury Rd, Westmead, NSW 2145, Australia
[2] Univ Sydney, Sydney, NSW, Australia
[3] Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne, Tyne & Wear, England
[4] Australia Plast Surg, Sydney, NSW, Australia
[5] Cosmet Culture, Pyrmont, NSW, Australia
[6] Pure Aesthet Plast Surg, Sydney, NSW, Australia
[7] Newcastle Hosp NHS Fdn Trust, Royal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
human; DC; macrophage; ex vivo; DERMAL DENDRITIC CELLS; LANGERHANS CELLS; ANTIGEN UPTAKE; HUMAN TISSUES; T-CELLS; HIV; MACROPHAGES; EXPRESSION; INFECTION; MOUSE;
D O I
10.1189/jlb.4A1116-496R
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Mononuclear phagocytes are present in skin and mucosa and represent one of the first lines of defense against invading pathogens, which they detect via an array of pathogen-binding receptors expressed on their surface. However, their extraction from tissue is difficult, and the isolation technique used has functional consequences on the cells obtained. Here, we compare mononuclear phagocytes isolated from human skin using either enzymatic digestion or spontaneous migration. Cells isolated via enzymatic digestion are in an immature state, and all subsets are easily defined. However, cells isolated by spontaneous migration are in a mature state, and CD141 cross-presenting DCs (cDC1) are more difficult to define. Different pathogen-binding receptors are susceptible to cleavage by blends of collagenase, demonstrating that great care must be taken in choosing the correct enzyme blend to digest tissue if carrying out pathogen-interaction assays. Finally, we have optimized mononuclear phagocyte culture conditions to enhance their survival after liberation from the tissue.
引用
收藏
页码:1393 / 1403
页数:11
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