Apoptosis: The sculptor of development

被引:43
作者
Doseff, AI [1 ]
机构
[1] Ohio State Univ, Dorothy M Davis Heart & Lung Res Inst, Columbus, OH 43210 USA
关键词
D O I
10.1089/scd.2004.13.473
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Apoptosis is a programmed mechanism of cell death recognized by its characteristic morphological and biochemical changes. Over the last decade, our understanding of the biochemistry of apoptosis has flourished. However, the physiological relevance of apoptosis remains elusive. Here, I propose that the process of programmed cell death plays an essential role in structural development. From pioneering studies almost a century ago to recent findings using modern technology, similar conclusions have emerged that highlight the fundamental role of apoptosis in vascular development. This review will recount these classic and modern studies as I survey evidence that implicates apoptosis in other aspects of development and ask how cell death can possibly contribute to homeostasis and development of the immune system. I briefly consider the mechanisms that may determine the fate of cells within the vasculature and propose new roles for the contribution of apoptosis to development and differentiation. More provocatively, I explore the possibilities that arise from this growing field of study, including prevention of developmental defects and even abnormal development after birth, such as neoplastic development. To realize these end points, the biochemical bases of apoptosis must be thoroughly understood.
引用
收藏
页码:473 / 483
页数:11
相关论文
共 111 条
[1]
RhoB controls Akt trafficking and stage-specific survival of endothelial cells during vascular development [J].
Adini, I ;
Rabinovitz, I ;
Sun, JF ;
Prendergast, GC ;
Benjamin, LE .
GENES & DEVELOPMENT, 2003, 17 (21) :2721-2732
[2]
The CD45 tyrosine phosphatase: a positive and negative regulator of immune cell function [J].
Alexander, DR .
SEMINARS IN IMMUNOLOGY, 2000, 12 (04) :349-359
[3]
Inhibition of caspase-9 through phosphorylation at Thr 125 by ERK MAPK [J].
Allan, LA ;
Morrice, N ;
Brady, S ;
Magee, G ;
Pathak, S ;
Clarke, PR .
NATURE CELL BIOLOGY, 2003, 5 (07) :647-U45
[4]
Transient occurrence of 27 kDa heat-shock protein in the terminal tubule cells during postnatal development of the rat submandibular gland [J].
Amano, O ;
Kudo, Y ;
Shimada, M ;
Wakayama, T ;
Yamamoto, M ;
Iseki, S .
ANATOMICAL RECORD, 2001, 264 (04) :358-366
[5]
ARENDS MJ, 1990, AM J PATHOL, V136, P593
[6]
Improved methods for the generation of dendritic cells from nonproliferating progenitors in human blood [J].
Bender, A ;
Sapp, M ;
Schuler, G ;
Steinman, RM ;
Bhardwaj, N .
JOURNAL OF IMMUNOLOGICAL METHODS, 1996, 196 (02) :121-135
[7]
Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death [J].
Boldin, MP ;
Goncharov, TM ;
Goltsev, YV ;
Wallach, D .
CELL, 1996, 85 (06) :803-815
[8]
The Bcl-2 protein family: sensors and checkpoints for life-or-death decisions [J].
Borner, C .
MOLECULAR IMMUNOLOGY, 2003, 39 (11) :615-647
[9]
Neural apoptosis [J].
Bredesen, DE .
ANNALS OF NEUROLOGY, 1995, 38 (06) :839-851
[10]
CD45-null transgenic mice reveal a positive regulatory role for CD45 in early thymocyte development, in the selection of CD4(+)CD8(+) thymocytes, and in B cell maturation [J].
Byth, KF ;
Conroy, LA ;
Howlett, S ;
Smith, AJH ;
May, J ;
Alexander, DR ;
Holmes, N .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (04) :1707-1718