Publications by authors named "P Lapinski"

Article Synopsis
  • - EPHB4 and RASA1 are essential for the formation and maintenance of lymphatic vessel (LV) valves during development, but how they interact in this process is not fully understood.
  • - The study used both genetically modified mice and human lymphatic endothelial cells to show that disrupting EPHB4 or RASA1 significantly impairs LV valve specification and development, which can be countered by targeting the Ras-MAPK signaling pathway.
  • - The findings indicate that proper function of EPHB4 and RASA1 is crucial for successful LV valve development, with potential implications for understanding lymphatic diseases or conditions related to valve dysfunction.
View Article and Find Full Text PDF

Ras guanine nucleotide-releasing protein 1 (Rasgrp1) is a Ras guanine nucleotide exchange factor that participates in the activation of the Ras-ERK signaling pathway in developing T cells and is required for efficient thymic T cell positive selection. However, the role of Rasgrp1 in mature peripheral T cells has not been definitively addressed, in part because peripheral T cells from constitutive Rasgrp1-deficient mice show an abnormal activated phenotype. In this study, we generated an inducible Rasgrp1-deficient mouse model to allow acute disruption of Rasgrp1 in peripheral CD4+ T cells in the context of normal T cell development.

View Article and Find Full Text PDF

Background: There is a need for a study of possible relationship between serving a prison sentence and developing postural stability dysfunction. The aim of the study was to analyze postural stability of physically inactive prisoners. The study group consisted of 24 male prisoners aged 34.

View Article and Find Full Text PDF

There is increasing interest in the study of the mammalian lymphatic system, including the lymphatic endothelial cells (LECs) that make up lymphatic vessels. The ability to isolate primary LECs from tissue of normal and genetically modified mice permits detailed analysis of this unique cell type. Here, we describe a robust protocol for the isolation and in vitro expansion of LECs from mouse lung by antibody-based magnetic separation.

View Article and Find Full Text PDF