Kim H, Yeger H, Han R, Wallace M, Goldstein B, Rotin D
Medical Research Council Group in Lung Development, Hospital for Sick Children, Toronto, Ontario, Canada.
Am J Physiol. 1996 Apr;270(4 Pt 1):L566-76. doi: 10.1152/ajplung.1996.270.4.L566.
The LAR family tyrosine phosphatase LAR-PTP2B (RPTP sigma) was previously shown to be expressed in the central and peripheral nervous system. Here we show that LAR-PTP2, the larger alternatively spliced form of the gene, is expressed in proliferating undifferentiated lung epithelia in a developmentally regulated manner: Using in situ hybridization and parallel immunostaining with proliferating cell nuclear antigen to detect proliferating cells, we demonstrate that LAR-PTP2 is expressed exclusively in the undifferentiated epithelial cell layer lining the bronchi, bronchioles, and air sacs in late fetal development and in the neonatal lung. These cells correspond to Clara and fetal alveolar type II cells, as determined by parallel immunostaining with antibodies to surfactant proteins A and B. LAR-PTP2 expression declined progressively with postnatal development, and by adult stage there was no detectable expression in the airways or in the distal (type I and II) mature nonproliferating alveolar epithelial cells. These results suggest that LAR-PTP2 may be involved in the regulation of epithelial cell proliferation/differentiation during lung development.
此前研究表明,LAR家族酪氨酸磷酸酶LAR-PTP2B(RPTP σ)在中枢和外周神经系统中表达。在此我们发现,该基因较大的可变剪接形式LAR-PTP2,以发育调控的方式在增殖的未分化肺上皮细胞中表达:通过原位杂交以及与增殖细胞核抗原进行平行免疫染色以检测增殖细胞,我们证明LAR-PTP2仅在胎儿发育后期和新生儿肺中,支气管、细支气管和气囊内衬的未分化上皮细胞层中表达。通过与表面活性蛋白A和B抗体进行平行免疫染色确定,这些细胞对应于克拉拉细胞和胎儿肺泡II型细胞。随着出生后发育,LAR-PTP2的表达逐渐下降,到成年阶段,在气道或远端(I型和II型)成熟的非增殖肺泡上皮细胞中未检测到表达。这些结果表明,LAR-PTP2可能参与肺发育过程中上皮细胞增殖/分化的调控。