Rysavy Noel M, Shimoda Lori M N, Dixon Alyssa M, Speck Mark, Stokes Alexander J, Turner Helen, Umemoto Eric Y
a Laboratory of Immunology and Signal Transduction ; Department of Biology; Chaminade University ; Honolulu , Hawai'i USA.
Bioarchitecture. 2014;4(4-5):127-37. doi: 10.1080/19490992.2014.995516.
Loss of plasma membrane asymmetry is a hallmark of apoptosis, but lipid bilayer asymmetry and loss of asymmetry can contribute to numerous cellular functions and responses that are independent of programmed cell death. Exofacial exposure of phosphatidylserine occurs in lymphocytes and mast cells after antigenic stimulation and in the absence of apoptosis, suggesting that there is a functional requirement for phosphatidylserine exposure in immunocytes. In this review we examine current ideas as to the nature of this functional role in mast cell activation. Mechanistically, there is controversy as to the candidate proteins responsible for phosphatidylserine translocation from the internal to external leaflet, and here we review the candidacies of mast cell PLSCR1 and TMEM16F. Finally we examine the potential relationship between functionally important mast cell membrane perturbations and phosphatidylserine exposure during activation.
质膜不对称性的丧失是细胞凋亡的一个标志,但脂质双分子层的不对称性及其丧失可促成许多与程序性细胞死亡无关的细胞功能和反应。在抗原刺激后且不存在细胞凋亡的情况下,淋巴细胞和肥大细胞中会出现磷脂酰丝氨酸的外表面暴露,这表明免疫细胞中磷脂酰丝氨酸暴露存在功能需求。在本综述中,我们研究了关于肥大细胞激活中这种功能作用性质的当前观点。在机制上,对于负责磷脂酰丝氨酸从内膜小叶向内膜小叶转运的候选蛋白存在争议,在此我们综述肥大细胞PLSCR1和TMEM16F作为候选蛋白的情况。最后,我们研究了肥大细胞激活过程中功能重要的细胞膜扰动与磷脂酰丝氨酸暴露之间的潜在关系。