Regulation of apoptosis by vasoactive peptides

被引:57
作者
Filippatos, GS
Gangopadhyay, N
Lalude, O
Parameswaran, N
Said, SI
Spielman, W
Uhal, BD
机构
[1] Michigan State Univ, Dept Physiol, E Lansing, MI 48824 USA
[2] Evangelismos Gen Hosp, Div Cardiol 2, GR-11526 Athens, Greece
[3] Case Western Reserve Univ, Metrohlth Med Ctr, Div Cardiol, Cleveland, OH 44106 USA
[4] Univ Med Ctr, Dept Med, Stony Brook, NY 11794 USA
[5] Vet Affairs Med Ctr, Northport, NY 11772 USA
关键词
programmed cell death; blood pressure; pulmonary pathophysiology; hypertension; lung fibrosis;
D O I
10.1152/ajplung.2001.281.4.L749
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Although originally discovered because of their ability to affect hemodynamics, vasoactive peptides have been found to function in a variety of capacities including neurotransmission, endocrine functions, and the regulation of cell proliferation. A growing body of evidence describes the ability of vasoactive peptides to regulate cell death by apoptosis in either a positive or negative fashion depending on the peptide and the type of target cell. The available evidence to date is strongest for the peptides endothelin, angiotensin II, vasoactive intestinal peptide, atrial natriuretic peptide, and adrenomedullin. Each of these peptides is discussed, with specific regard to apoptosis, in terms of regulatory activity, target cell specificity, and potential role in pulmonary physiology.
引用
收藏
页码:L749 / L761
页数:13
相关论文
共 133 条
  • [81] Immunobiology of vasoactive intestinal peptide (VIP)
    Pozo, D
    Delgado, M
    Martínez, C
    Guerrero, JM
    Leceta, J
    Gomariz, RP
    Calvo, JR
    [J]. IMMUNOLOGY TODAY, 2000, 21 (01): : 7 - 11
  • [82] Bcl-2 family proteins
    Reed, JC
    [J]. ONCOGENE, 1998, 17 (25) : 3225 - 3236
  • [83] RYAN JW, 1975, BIOCHEM J, V146, P497, DOI 10.1042/bj1460497
  • [84] Pathways of inflammation and cell death in the lung: modulation by vasoactive intestinal peptide
    Said, SI
    Dickman, KG
    [J]. REGULATORY PEPTIDES, 2000, 93 (1-3) : 21 - 29
  • [85] Excitotoxicity in the lung: N-methyl-D-aspartate-induced, nitric oxide-dependent, pulmonary edema is attenuated by vasoactive intestinal peptide and by inhibitors of poly(ADP-ribose) polymerase
    Said, SI
    Berisha, HI
    Pakbaz, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (10) : 4688 - 4692
  • [86] Molecules that protect: The defense of neurons and other cells
    Said, SI
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (10) : 2163 - 2164
  • [87] Glutamate toxicity in the lung and neuronal cells: Prevention or attenuation by VIP and PACAP
    Said, SI
    Dickman, K
    Dey, RD
    Bandyopadhyay, A
    De Stefanis, P
    Raza, S
    Pakbaz, H
    Berisha, HI
    [J]. VIP, PACAP, AND RELATED PEPTIDES: THIRD INTERNATIONAL SYMPOSIUM, 1998, 865 : 226 - 237
  • [88] SAID SI, 1998, LUNG BIOL HEALTH DIS, V112, P345
  • [89] Mitogenic activity of endothelin on human cultured prostatic smooth muscle cells
    Saita, Y
    Yazawa, H
    Koizumi, T
    Morita, T
    Tamura, T
    Takenaka, T
    Honda, K
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 349 (01) : 123 - 128
  • [90] Inhibition of myocardial endothelin pathway improves long-term survival in heart failure
    Sakai, S
    Miyauchi, T
    Kobayashi, M
    Yamaguchi, I
    Goto, K
    Sugishita, Y
    [J]. NATURE, 1996, 384 (6607) : 353 - 355