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特发性肺动脉高压中的平滑肌表型:高增殖但非癌变。

Smooth Muscle Phenotype in Idiopathic Pulmonary Hypertension: Hyper-Proliferative but not Cancerous.

机构信息

Université Paris-Sud, Faculté de Médecine, 94270 Kremlin-Bicêtre, France.

Assistance Publique-Hôpitaux de Paris (AP-HP), Centre de Référence de l'Hypertension Pulmonaire Sévère, Département Hospitalo-Universitaire Thorax Innovation, Service de Pneumologie et Réanimation Respiratoire, Hôpital de Bicêtre, 94270 Le Kremlin-Bicêtre, France.

出版信息

Int J Mol Sci. 2019 Jul 22;20(14):3575. doi: 10.3390/ijms20143575.

DOI:10.3390/ijms20143575
PMID:31336611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6679125/
Abstract

Idiopathic pulmonary arterial hypertension (IPAH) is a complex disease associated with vascular remodeling and a proliferative disorder in pulmonary artery smooth muscle cells (PASMCs) that has been variably described as having neoplastic features. To decode the phenotype of PASMCs in IPAH, PASMCs from explanted lungs of patients with IPAH (IPAH-PASMCs) and from controls (C-PASMCs) were cultured. The IPAH-PASMCs grew faster than the controls; however, both growth curves plateaued, suggesting contact inhibition in IPAH cells. No proliferation was seen without stimulation with exogenous growth factors, suggesting that IPAH cells are incapable of self-sufficient growth. IPAH-PASMCs were more resistant to apoptosis than C-PASMCs, consistent with the increase in the Bcl2/Bax ratio. As cell replication is governed by telomere length, these parameters were assessed jointly. Compared to C-PASMCs, IPAH-PASMCs had longer telomeres, but a limited replicative capacity. Additionally, it was noted that IPAH-PASMCs had a shift in energy production from mitochondrial oxidative phosphorylation to aerobic glycolysis. As DNA damage and genomic instability are strongly implicated in IPAH development a comparative genomic hybridization was performed on genomic DNA from PASMCs which showed multiple break-points unaffected by IPAH severity. Activation of DNA damage/repair factors (γH2AX, p53, and GADD45) in response to cisplatin was measured. All proteins showed lower phosphorylation in IPAH samples than in controls, suggesting that the cells were resistant to DNA damage. Despite the cancer-like processes that are associated with end-stage IPAH-PASMCs, we identified no evidence of self-sufficient proliferation in these cells-the defining feature of neoplasia.

摘要

特发性肺动脉高压(IPAH)是一种与血管重构相关的复杂疾病,伴有肺动脉平滑肌细胞(PASMC)的增殖紊乱,其具有肿瘤特征,这一特征已得到不同程度的描述。为了解析 IPAH 中 PASMC 的表型,我们培养了源自 IPAH 患者(IPAH-PASMC)和对照者(C-PASMC)的肺组织中分离出的 PASMC。与对照组相比,IPAH-PASMC 的生长速度更快;然而,两组的生长曲线都达到了平台期,提示 IPAH 细胞存在接触抑制。在没有外源性生长因子刺激的情况下,没有观察到增殖,这表明 IPAH 细胞无法进行自我充足的生长。与 C-PASMC 相比,IPAH-PASMC 对细胞凋亡的抵抗能力更强,这与 Bcl2/Bax 比值的增加一致。由于细胞复制受端粒长度的控制,我们联合评估了这些参数。与 C-PASMC 相比,IPAH-PASMC 的端粒更长,但复制能力有限。此外,我们注意到 IPAH-PASMC 的能量产生从线粒体氧化磷酸化向有氧糖酵解转移。由于 DNA 损伤和基因组不稳定性在 IPAH 的发展中起着重要作用,我们对源自 PASMC 的基因组 DNA 进行了比较基因组杂交分析,结果显示多个断裂点不受 IPAH 严重程度的影响。我们还测量了顺铂刺激下 DNA 损伤/修复因子(γH2AX、p53 和 GADD45)的激活情况。所有蛋白在 IPAH 样本中的磷酸化水平均低于对照组,表明细胞对 DNA 损伤具有抗性。尽管与晚期 IPAH-PASMC 相关的过程具有癌症样特征,但我们没有发现这些细胞具有自我充足增殖的证据——这是肿瘤的定义特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/401fe21d1c72/ijms-20-03575-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/2de9818d1005/ijms-20-03575-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/8b6433d37904/ijms-20-03575-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/92206676e35c/ijms-20-03575-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/224c8309dfff/ijms-20-03575-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/401fe21d1c72/ijms-20-03575-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/2de9818d1005/ijms-20-03575-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/8017a9dccab7/ijms-20-03575-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/8b6433d37904/ijms-20-03575-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/92206676e35c/ijms-20-03575-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/224c8309dfff/ijms-20-03575-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b790/6679125/401fe21d1c72/ijms-20-03575-g006.jpg

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