Dalton Cardiovascular Research Center, University of Missouri-Columbia, Columbia, MO 65211, USA.
Biochem J. 2012 Apr 1;443(1):185-91. doi: 10.1042/BJ20111881.
CypD (cyclophilin D) has been established as a critical regulator of the MPT (mitochondrial permeability transition) pore, and pharmacological or genetic inhibition of CypD attenuates MPT in numerous systems. However, it has recently been suggested that the inhibitory effects of CypD inhibition only manifest when P(i) (inorganic phosphate) is present, and that inhibition is lost when P(i) is replaced by As(i) (inorganic arsenate) or V(i) (inorganic vanadate). To test this, liver mitochondria were isolated from wild-type and CypD-deficient (Ppif-/-) mice and then incubated in buffer containing P(i), As(i) or V(i). MPT was induced under both energized and de-energized conditions by the addition of Ca2+, and the resultant mitochondrial swelling was measured spectrophotometrically. For pharmacological inhibition of CypD, wild-type mitochondria were pre-incubated with CsA (cyclosporin A) before the addition of Ca2+. In energized and de-energized mitochondria, Ca2+ induced MPT regardless of the anion present, although the magnitude differed between P(i), As(i) and V(i). However, in all cases, pre-treatment with CsA significantly inhibited MPT. Moreover, these effects were independent of mouse strain, organ type and rodent species. Similarly, attenuation of Ca2+-induced MPT in the Ppif-/- mitochondria was still observed irrespective of whether P(i), As(i) or V(i) was present. We conclude that the pharmacological and genetic inhibition of CypD is still able to attenuate MPT even in the absence of P(i).
CypD(亲环素 D)已被确定为 MPT(线粒体通透性转换)孔的关键调节因子,药理学或遗传学抑制 CypD 可减轻许多系统中的 MPT。然而,最近有人提出,CypD 抑制的抑制作用仅在存在 P(i)(无机磷酸盐)时才表现出来,并且当 P(i)被 As(i)(无机砷酸盐)或 V(i)(无机钒酸盐)取代时,抑制作用就会丧失。为了验证这一点,从野生型和 CypD 缺陷型(Ppif-/-)小鼠中分离出线粒体,然后在含有 P(i)、As(i)或 V(i)的缓冲液中孵育。通过添加 Ca2+,在有能量和无能量的条件下诱导 MPT,然后通过分光光度法测量线粒体肿胀。对于 CypD 的药理学抑制,在添加 Ca2+之前,用 CsA(环孢菌素 A)预孵育野生型线粒体。在有能量和无能量的线粒体中,Ca2+诱导 MPT 与存在的阴离子无关,尽管 P(i)、As(i)和 V(i)之间的大小有所不同。然而,在所有情况下,CsA 的预处理都显著抑制了 MPT。此外,这些影响与小鼠品系、器官类型和啮齿动物种类无关。同样,在无论是否存在 P(i)、As(i)或 V(i)的情况下,仍观察到 Ppif-/- 线粒体中 Ca2+诱导的 MPT 减弱。我们得出结论,即使在没有 P(i)的情况下,CypD 的药理学和遗传学抑制仍然能够减轻 MPT。