Detection of bone marrow-derived lung epithelial cells.
Detection of bone marrow-derived lung epithelial cells.
复制标题
DOI:
10.1016/j.exphem.2010.04.011
复制
发表时间:
2010-07
影响因子:
2.6
通讯作者:
Krause, Diane S.
中科院分区:
文献类型:
--
作者:
Kassmer, Susannah H.;Krause, Diane S.
Studies on the ability of bone marrow derived cells to adopt the morphology and protein expression of epithelial cells in vivo have expanded rapidly over the last decade, and hundreds of publications report that bone marrow derived cells can become epithelial cells of multiple organs including lung, liver, GI tract, skin, pancreas and others. In this review, we critically evaluate the literature related to engraftment of bone marrow derived cells as epithelial cells in the lung. Over 40 manuscripts focused on whether bone marrow cells can differentiate into lung epithelial cells have been published, nearly all of which claim to identify marrow derived epithelial cells. A few investigations have concluded that no such cells are present and that the phenomenon of marrow derived epithelial cells is based on detection artifacts. Here we discuss the problems that exist in published papers identifying marrow derived epithelial cells, and propose standards for detection methods that provide the most definitive data. Identification of BM derived epithelial cells requires reliable and sensitive techniques for their detection, which must include cell identification based on the presence of an epithelial marker and the absence of blood cell markers as well as a marker for donor BM origin. In order for these studies to be rigorous, they must also use approaches to rule out cell overlap by microscopy or single cell isolation. Once these stringent criteria for identification of marrow derived epithelial cells are used universally, then the field can move forward to address the critical questions regarding which bone marrow derived cells are responsible for engraftment as epithelial cells, the mechanisms by which this occurs, whether these cells play a role in normal tissue repair, and whether specific cell subsets can be used for therapeutic benefit.
登录
查看更多内容
影响因子:
5.8
作者:
Lee SH;Jang AS;Kim YE;Cha JY;Kim TH;Jung S;Park SK;Lee YK;Won JH;Kim YH;Park CS
通讯作者:
Park CS
DOI:
10.1164/rccm.200902-0242oc
发表时间:
2009-12-01
影响因子:
24.7
作者:
Aslam, Muhammad;Baveja, Rajiv;Kourembanas, Stella
通讯作者:
Kourembanas, Stella
DOI:
10.1165/rcmb.2002-0056rc
发表时间:
2002-12-01
影响因子:
6.4
作者:
Grove, JE;Lutzko, C;Krause, DS
通讯作者:
Krause, DS
DOI:
10.1073/pnas.95.4.1579
发表时间:
1998-02-17
影响因子:
11.1
作者:
Haller, T;Ortmayr, J;Dietl, P
通讯作者:
Dietl, P
影响因子:
4
作者:
MacPherson, H;Keir, P;Dorin, J
通讯作者:
Dorin, J