A.D. Merritt

Urinary pepsinogen isozymes: A highly polymorphic locus in man

SummaryA genetic analysis of human urinary pepsinogen isozymes is presented. Nine discrete phenotypes were identified in a population survey of 215 unrelated Caucasian individuals. The phenotypes were characterized by differences among the staining intensities of the activated group I pepsinogens, Pg 5, Pg 4, Pg 3, and Pg 2. The genetic studies demonstrated that the codominant expression of four alleles, PgA, PgB, PgC and PgD, at a single genetic locus determined the nine phenotypes identified. Linkage analysis excluded close linkage of the Pg locus with the chromosome 6 markers HLA, GLO1, and Bf.

Immunohistochemical demonstration of the loss of immunoreactive amylase from neoplastic human salivary gland

Antihuman parotid amylase antibodies raised in rabbits and horses were used as the primary antibodies in both the peroxidase-antiperoxidase and sandwich techniques for the localization of human amylase. Immunoreactive enzyme was demonstrated in the normal acinar cells of salivary glands and pancreas. Malignant transformation, which has occasionally resulted in ectopic production of amylase by various tissues, actually caused a loss of amylase synthesis by the transformed acinar cells of salivary glands and did not result in elaboration of amylase by transformed ductal cells.