Raffaniello R D, Lin J, Wang F, Raufman J P
Department of Medicine, State University of New York-Health Science Center at Brooklyn 11203-2098, USA.
Biochim Biophys Acta. 1996 Apr 24;1311(2):111-6. doi: 10.1016/0167-4889(95)00204-9.
Rab3 proteins are low molecular weight GTP-binding proteins that are expressed in neurons and other secretory cells. These proteins are localized to secretory vesicles and may play a role in regulated exocytosis. Presently, four highly homologous Rab3 isoforms (A, B, C, D) have been identified. We examined the expression of Rab3 isoforms in dispersed chief cells from guinea pig stomach. Immunoblotting with a specific monoclonal Rab3 antibody detected a 27-kDa protein in chief cell cytosolic and membrane fractions, but staining was more intense in membrane fractions. Using the Rab3 antibody, immunohistochemical staining was detected in chief cells but not in parietal or mucous cells. To determine which Rab3 isoform(s) is (are) expressed, chief cell cDNA was obtained by reverse transcription and subjected to PCR using degenerate primers that are specific for rab3 isoforms. The resulting PCR products were cloned and sequenced. The nucleotide sequences obtained were 89% homologous to the nucleotide sequence of mouse rab3D. The deduced amino acid sequence was identical to that of mouse Rab3D (amino acids 16-83). Moreover, Rab3D was the only isoform detected in chief cells by these methods. To identify rab3 transcripts, the guinea pig rab3D fragment obtained by reverse transcription PCR cloning was used as a probe for Northern blotting. The 4.0- and 2.3-kb transcripts identified in chief cells with the rab3 probe were the same size as those detected by others in mouse adipocytes using a rab3D-specific probe. These results indicate that Rab3D is expressed in gastric chief cells.
Rab3蛋白是低分子量的GTP结合蛋白,在神经元和其他分泌细胞中表达。这些蛋白定位于分泌小泡,可能在调节性胞吐作用中发挥作用。目前,已鉴定出四种高度同源的Rab3亚型(A、B、C、D)。我们检测了豚鼠胃分散主细胞中Rab3亚型的表达。用特异性单克隆Rab3抗体进行免疫印迹,在主细胞胞质和膜组分中检测到一种27 kDa的蛋白,但膜组分中的染色更强。使用Rab3抗体,在主细胞中检测到免疫组化染色,而在壁细胞或黏液细胞中未检测到。为了确定表达的是哪种Rab3亚型,通过逆转录获得主细胞cDNA,并使用对rab3亚型特异的简并引物进行PCR。将所得的PCR产物克隆并测序。获得的核苷酸序列与小鼠rab3D的核苷酸序列同源性为89%。推导的氨基酸序列与小鼠Rab3D(氨基酸16 - 83)相同。此外,通过这些方法在主细胞中检测到的唯一亚型是Rab3D。为了鉴定rab3转录本,将通过逆转录PCR克隆获得的豚鼠rab3D片段用作Northern印迹的探针。用rab3探针在主细胞中鉴定出的4.0 kb和2.3 kb转录本与其他人使用rab3D特异性探针在小鼠脂肪细胞中检测到的转录本大小相同。这些结果表明Rab3D在胃主细胞中表达。