Expression of pregnancy-specific beta 1-glycoprotein genes in hematopoietic cells

• Published in: Molecular and cellular biochemistry Vol. 122; no. 2; pp. 147 - 158
• Main Authors: Wu, S M, Bazar, L S, Cohn, M L, Cahill, R A, Chan, W Y
• Format: Journal Article
• Language: English
• Published: Netherlands 26-05-1993
• Subjects: Alternative Splicing - physiology; Base Sequence; Female; Gene Expression; Hematopoietic Stem Cells - metabolism; Humans; Molecular Sequence Data; Placenta - metabolism; Pregnancy; Pregnancy-Specific beta 1-Glycoproteins - genetics; RNA, Messenger - biosynthesis; T-Lymphocytes - metabolism
• ISSN: 0300-8177
• DOI: 10.1007/BF01076099

The presence of PSG in blood cells has been demonstrated by immunohistochemical staining. However, the origin of those proteins is not known. This report examines the expression of the PSG genes in different types of freshly isolated blood cells. RNA isolated from bone marrow and peripheral blood cells of healthy individuals was analyzed for PSG transcripts by reverse transcriptase-polymerase chain reaction using synthetic oligonucleotide primers specific for the PSG genes. The level of expression of the PSG genes in different types of cells exhibited significant individual variation. Trace amounts of PSG transcripts could be detected in polymorphonuclear cells (PMN), monocytes and B lymphocytes while T lymphocytes always contained the highest level of transcript. The expression of PSG genes in the blood cells apparently was not affected by the method of isolation nor by overnight culturing of these cells except in the case when lymphocytes were separated by rosetting with sheep red blood cells. All reported PSG transcripts were detected in blood cells. Both type I and type II transcripts of the PSG genes were detected in blood cells with the exception of type II transcript of PSG5 and PSG11 which were only found in the placenta. Tissue specificity in the expression or alternative splicing of some of the PSG family members was implicated.