Kárpáti S, Amagai M, Prussick R, Cehrs K, Stanley J R
National Cancer Institute, Dermatology Branch, NIH, Bethesda, Md 20892.
J Cell Biol. 1993 Jul;122(2):409-15. doi: 10.1083/jcb.122.2.409.
Pemphigus vulgaris antigen (PVA) is a member of the desmoglein subfamily of cadherin cell adhesion molecules. Because autoantibodies in this disease cause blisters due to loss of epidermal cell adhesion, and because desmoglein is found in the desmosome cell adhesion junction, we wanted to determine if PVA is also found in desmosomes. By immunofluorescence, PV IgG bound, in a dotted pattern, to the cell surface of cultured human keratinocytes induced to differentiate with calcium, suggesting junctional staining. However, by preembedding, immunogold electron microscopic studies only slight labeling could be detected in desmosomes, presumably because of difficulty in gold penetration of intact desmosomes. We therefore treated the keratinocytes with 0.01% trypsin in 1 mM calcium, conditions known to preserve cadherin antigenicity but that caused slight separation of desmosomes, before immunogold staining. In this case there was extensive labeling of the extracellular part of desmosomes but not of the interdesmosomal cell membrane which was stained with anti-beta 2-microglobulin antibodies. To confirm the specificity of this binding we showed that antibodies raised in rabbits against the extracellular portions of PVA also bound desmosomes in these cultures. In intact mouse epidermis we could also show slight, but specific, immunogold desmosomal labeling with PV IgG. Furthermore, neonatal mice injected with PV IgG affinity purified on PVA showed desmosomal separation with the IgG localized to desmosomal cores. These results indicate that PVA is organized and concentrated within the desmosome where it presumably functions to maintain the integrity of stratifying epithelia.
寻常型天疱疮抗原(PVA)是钙黏蛋白细胞黏附分子桥粒芯糖蛋白亚家族的成员。由于该疾病中的自身抗体因表皮细胞黏附丧失而导致水疱形成,且桥粒芯糖蛋白存在于桥粒细胞黏附连接中,我们想确定PVA是否也存在于桥粒中。通过免疫荧光法,PV IgG以点状模式结合到经钙诱导分化的培养人角质形成细胞的细胞表面,提示有连接染色。然而,通过包埋前免疫金电子显微镜研究,仅在桥粒中检测到轻微标记,推测是由于完整桥粒对金的穿透困难。因此,在免疫金染色前,我们用含1 mM钙的0.01%胰蛋白酶处理角质形成细胞,已知该条件可保留钙黏蛋白抗原性,但会导致桥粒轻微分离。在这种情况下,桥粒的细胞外部分有广泛标记,但桥粒间细胞膜未被标记,而用抗β2 -微球蛋白抗体可对其进行染色。为证实这种结合的特异性,我们表明用针对PVA细胞外部分制备的兔抗体也能结合这些培养物中的桥粒。在完整的小鼠表皮中,我们也能用PV IgG显示轻微但特异的免疫金桥粒标记。此外,注射用PVA亲和纯化的PV IgG的新生小鼠显示桥粒分离,IgG定位于桥粒核心。这些结果表明,PVA在桥粒内有序排列并浓缩,其可能在维持复层上皮的完整性方面发挥作用。