Susan D'Costa1, Luke Borst, Yongbaek Kim. 1. The Laboratory of Clinical Pathology, College of Veterinary Medicine, Seoul National University,1 Gwanak-ro, Gwanak-gu, Seoul 151-742, The Republic of Korea.
Abstract
UNLABELLED: BACKGROUND/ AIM: The present study was performed in order to investigate the distribution of transplanted bone marrow-derived cells (BMDCs) in normal and neoplastic tissues. MATERIALS AND METHODS: A microchimeric mouse model harboring traceable BMDCs was created by injecting labeled BMDCs into adenovirus-expressing Cre (AdenoCre)-infected, irradiated, LSL-K-ras(G12D) p53(fl/fl) mice. RESULTS: In the normal mice, transplanted cells were detected in the femur, tibia, lung, heart, kidney and spleen of recipient mice. The transplanted BMDCs were detected predominantly in the connective tissue around the smaller bronchioles of normal lung parenchyma. In the lung tumor-bearing mice, the transplanted BMDCs were detected within the tumor tissue and more abundantly in the connective tissue adjacent to the tumor mass. CONCLUSION: This study provides morphological evidence of a microchimeric experimental system that may promote further research into the role of BMDCs in the carcinogenic process and for the development of a novel therapy aimed at targeting stromal cells and, eventually, tumor growth.
UNLABELLED: BACKGROUND/ AIM: The present study was performed in order to investigate the distribution of transplanted bone marrow-derived cells (BMDCs) in normal and neoplastic tissues. MATERIALS AND METHODS: A microchimeric mouse model harboring traceable BMDCs was created by injecting labeled BMDCs into adenovirus-expressing Cre (AdenoCre)-infected, irradiated, LSL-K-ras(G12D) p53(fl/fl) mice. RESULTS: In the normal mice, transplanted cells were detected in the femur, tibia, lung, heart, kidney and spleen of recipient mice. The transplanted BMDCs were detected predominantly in the connective tissue around the smaller bronchioles of normal lung parenchyma. In the lung tumor-bearing mice, the transplanted BMDCs were detected within the tumor tissue and more abundantly in the connective tissue adjacent to the tumor mass. CONCLUSION: This study provides morphological evidence of a microchimeric experimental system that may promote further research into the role of BMDCs in the carcinogenic process and for the development of a novel therapy aimed at targeting stromal cells and, eventually, tumor growth.