Lesseps R J
J Cell Biol. 1967 Jul;34(1):173-83. doi: 10.1083/jcb.34.1.173.
Fixation of embryonic chick cells (heart, neural retina, and limb bud) in the presence of lanthanum ions shows the presence of an electron-opaque layer, about 50 A thick, external to the cell membrane. This layer, designated LSM (for lanthanum-staining material), is not removable by trypsin, pronase, EDTA, DNase, alpha-amylase, neuraminidase, or N-acetyl-L-cysteine. However, phospholipase C, in concentrations as low as 0.001 mg/ml, succeeds in stripping the LSM from the cell surface. Heating the enzyme preparation does not inhibit this activity, but removal of divalent cations does; both of these results are consistent with the known properties of phospholipase C. The LSM is present at the cell surface in the control tissues and on cells dissociated from the tissues by proteolytic enzymes and EDTA. These results are interpreted to mean that the LSM is probably an integral part of the cell and not an extraneous coat. How this phenomenon bears on the problem of cellular adhesion is discussed, as is the possible chemical composition of the LSM.
在镧离子存在的情况下对鸡胚细胞(心脏、神经视网膜和肢芽)进行固定,结果显示在细胞膜外部存在一层约50埃厚的电子致密层。这一层被命名为LSM(镧染色物质),用胰蛋白酶、链霉蛋白酶、乙二胺四乙酸(EDTA)、脱氧核糖核酸酶(DNase)、α-淀粉酶、神经氨酸酶或N-乙酰-L-半胱氨酸都无法去除。然而,浓度低至0.001毫克/毫升的磷脂酶C却能成功地将LSM从细胞表面剥离。加热酶制剂不会抑制这种活性,但去除二价阳离子则会抑制;这两个结果都与磷脂酶C的已知特性相符。在对照组织的细胞表面以及通过蛋白水解酶和EDTA从组织中解离出来的细胞上都存在LSM。这些结果被解释为意味着LSM可能是细胞的一个组成部分,而不是外来的被膜。本文讨论了这一现象与细胞黏附问题的关系,以及LSM可能的化学组成。