Development and function of the mammalian spleen

被引:153
作者
Brendolan, Andrea
Rosado, Maria Manuela
Carsetti, Rita
Selleri, Licia
Dear, T. Neil
机构
[1] Univ Sheffield, Sch Med & Biomed Sci, Mammalian Genet Dis Unit, Sheffield S10 2RX, S Yorkshire, England
[2] Cornell Univ, Dept Cell & Dev Biol, Weill Med Sch, Ithaca, NY 14853 USA
[3] Osped Pediat Bambino Gesu, IRCCS, Res Ctr, Rome, Italy
关键词
D O I
10.1002/bies.20528
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The vertebrate spleen has important functions in immunity and haematopoiesis, many of which have been well studied. In contrast, we know much less about the mechanisms governing its early embryonic development. However, as a result of work over the past decade-mostly using knockout mice-significant progress has been made in unravelling the genetic processes governing the spleen's early development. Key genetic regulators, such as Tlx1 and Pbx1, have been identified, and we know some of the early transcriptional hierarchies that control the early patterning and proliferation of the splenic primordium. In mouse and humans, asplenia can arise as a result of laterality defects, or the spleen can be absent with no other discernible abnormalities. Surprisingly, given the spleen's diverse functions, asplenic individuals suffer no major haematopoietic or immune defects apart from a susceptibility to infection with encapsulated bacteria. Recent evidence has shed light on a previously unknown role of the spleen in the development and maintenance of specific B cell populations that are involved in the initial response to infection caused by encapsulated bacteria. The lack of these populations in asplenic mice and humans may go some way to explaining this susceptibility. (c) 2007 Wiley Periodicals, Inc.
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页码:166 / 177
页数:12
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