• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

表面活性蛋白C在大鼠肺的II型肺泡细胞中表达,但在克拉拉细胞中不表达。

Surfactant protein C is expressed in alveolar type II cells but not in Clara cells of rat lung.

作者信息

Kalina M, Mason R J, Shannon J M

机构信息

Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.

出版信息

Am J Respir Cell Mol Biol. 1992 Jun;6(6):594-600. doi: 10.1165/ajrcmb/6.6.594.

DOI:10.1165/ajrcmb/6.6.594
PMID:1591008
Abstract

The expression of the surfactant-associated proteins in bronchiolar cells remains to be defined. We used in situ hybridization to identify sites of message expression of the surfactant-associated proteins A, B, and C (SP-A, SP-B, and SP-C) in adult and fetal rat lung. The expression of these messages by in situ hybridization was also compared with the localization of SP-A by immunocytochemistry. The localization of SP-A was used to identify type II cells and nonciliated bronchiolar epithelial (Clara) cells in these sections. The cRNA antisense probes for SP-A, SP-B, and SP-C appeared to hybridize over type II cells. Sense probes showed no localization or apparent specific hybridization. Messages for both SP-A and SP-B were also found in nonciliated bronchiolar epithelial (Clara) cells. However, no message for SP-C was observed in these cells. Clara cells from terminal to large bronchioles lacked detectable mRNA for SP-C. Expression of surfactant protein mRNAs was not detectable in type I cells, alveolar macrophages, interstitial cells, or vascular cells. Similarly, in fetal rat lung the messages for SP-A and SP-B but not SP-C were detected in bronchiolar cells. We conclude that rat Clara cells do not express SP-C mRNA, and thus SP-C can be regarded as a specific marker for rat type II cells.

摘要

支气管细胞中表面活性物质相关蛋白的表达情况仍有待明确。我们采用原位杂交技术来确定成年和胎鼠肺中表面活性物质相关蛋白A、B和C(SP-A、SP-B和SP-C)的信使表达位点。通过原位杂交对这些信使的表达情况与免疫细胞化学法检测的SP-A定位情况进行了比较。利用SP-A的定位来识别这些切片中的Ⅱ型细胞和无纤毛支气管上皮(克拉拉)细胞。用于SP-A、SP-B和SP-C的cRNA反义探针似乎在Ⅱ型细胞上发生杂交。正义探针未显示出定位或明显的特异性杂交信号。在无纤毛支气管上皮(克拉拉)细胞中也发现了SP-A和SP-B的信使。然而,在这些细胞中未观察到SP-C的信使。从终末细支气管到大气道的克拉拉细胞均缺乏可检测到的SP-C mRNA。在Ⅰ型细胞、肺泡巨噬细胞、间质细胞或血管细胞中未检测到表面活性物质蛋白mRNA的表达。同样,在胎鼠肺中,在支气管细胞中检测到了SP-A和SP-B的信使,但未检测到SP-C的信使。我们得出结论,大鼠克拉拉细胞不表达SP-C mRNA,因此SP-C可被视为大鼠Ⅱ型细胞的特异性标志物。

相似文献

1
Surfactant protein C is expressed in alveolar type II cells but not in Clara cells of rat lung.表面活性蛋白C在大鼠肺的II型肺泡细胞中表达,但在克拉拉细胞中不表达。
Am J Respir Cell Mol Biol. 1992 Jun;6(6):594-600. doi: 10.1165/ajrcmb/6.6.594.
2
Differential expressions of surfactant protein SP-A, SP-B, and SP-C mRNAs in rats with streptozotocin-induced diabetes demonstrated by in situ hybridization.原位杂交法显示链脲佐菌素诱导的糖尿病大鼠中表面活性蛋白SP-A、SP-B和SP-C mRNA的差异表达。
Am J Respir Cell Mol Biol. 1994 Oct;11(4):397-404. doi: 10.1165/ajrcmb.11.4.7917308.
3
Localization of surfactant-associated proteins SP-A and SP-B mRNA in rabbit fetal lung tissue by in situ hybridization.通过原位杂交技术对兔胎儿肺组织中表面活性物质相关蛋白SP-A和SP-B mRNA进行定位。
Am J Respir Cell Mol Biol. 1992 Sep;7(3):335-43. doi: 10.1165/ajrcmb/7.3.335.
4
Surfactant apoprotein A (SP-A) is synthesized in airway cells.表面活性物质载脂蛋白A(SP-A)在气道细胞中合成。
Am J Respir Cell Mol Biol. 1990 Nov;3(5):491-6. doi: 10.1165/ajrcmb/3.5.491.
5
Differential accumulation of surfactant protein A, B, and C mRNAs in two epithelial cell types of hyperoxic lung.表面活性蛋白A、B和C mRNA在高氧肺的两种上皮细胞类型中的差异积累。
Am J Respir Cell Mol Biol. 1991 Dec;5(6):511-5. doi: 10.1165/ajrcmb/5.6.511.
6
Overexpression of pulmonary surfactant apoprotein A mRNA in alveolar type II cells and nonciliated bronchiolar (Clara) epithelial cells in streptozotocin-induced diabetic rats demonstrated by in situ hybridization.通过原位杂交证实链脲佐菌素诱导的糖尿病大鼠肺泡II型细胞和无纤毛细支气管(克拉拉)上皮细胞中肺表面活性物质载脂蛋白A mRNA的过表达。
Am J Respir Cell Mol Biol. 1992 Mar;6(3):307-14. doi: 10.1165/ajrcmb/6.3.307.
7
Glucocorticoid regulation of surfactant-associated proteins in rabbit fetal lung in vivo.糖皮质激素对兔胎儿肺表面活性物质相关蛋白的体内调节作用。
Anat Rec. 1993 Nov;237(3):365-77. doi: 10.1002/ar.1092370310.
8
Overexpression of surfactant protein SP-A, SP-B, and SP-C mRNA in rat lungs with lipopolysaccharide-induced injury.脂多糖诱导损伤大鼠肺中表面活性蛋白SP-A、SP-B和SP-C mRNA的过表达。
Lab Invest. 1996 Jan;74(1):209-20.
9
Localization and developmental expression of surfactant proteins D and A in the respiratory tract of the mouse.表面活性蛋白D和A在小鼠呼吸道中的定位及发育表达
Pediatr Res. 1996 Jun;39(6):930-7. doi: 10.1203/00006450-199606000-00002.
10
Temporal-spatial distribution of SP-B and SP-C proteins and mRNAs in developing respiratory epithelium of human lung.人肺发育中呼吸上皮内表面活性蛋白B和表面活性蛋白C的时空分布及mRNA表达
J Histochem Cytochem. 1994 Sep;42(9):1187-99. doi: 10.1177/42.9.8064126.

引用本文的文献

1
Histopathological and Immunohistochemical Study of Neoplastic Cell Heterogeneity in Early and Advanced Ovine Pulmonary Adenocarcinoma.绵羊早期和晚期肺腺癌肿瘤细胞异质性的组织病理学和免疫组织化学研究
Animals (Basel). 2025 Sep 8;15(17):2632. doi: 10.3390/ani15172632.
2
Discovering genes and microRNAs involved in human lung development unveils IGFBP3/miR-34a dynamics and their relevance for alveolar differentiation.揭示人类肺发育过程中涉及的基因和 microRNAs,揭示 IGFBP3/miR-34a 的动态及其对肺泡分化的相关性。
Stem Cell Res Ther. 2024 Aug 26;15(1):263. doi: 10.1186/s13287-024-03883-1.
3
Ferroptotic alveolar epithelial type II cells drive T2 and T17 mixed asthma triggered by birch pollen allergen Bet v 1.
铁死亡的II型肺泡上皮细胞驱动由桦树花粉过敏原Bet v 1引发的T2和T17混合型哮喘。
Cell Death Discov. 2024 Feb 23;10(1):96. doi: 10.1038/s41420-024-01861-3.
4
A promoterless AAV6.2FF-based lung gene editing platform for the correction of surfactant protein B deficiency.一种基于无启动子AAV6.2FF的肺基因编辑平台,用于纠正表面活性物质蛋白B缺乏症。
Mol Ther. 2023 Dec 6;31(12):3457-3477. doi: 10.1016/j.ymthe.2023.10.002. Epub 2023 Oct 7.
5
Influenza virus decreases albumin uptake and megalin expression in alveolar epithelial cells.流感病毒降低肺泡上皮细胞对白蛋白的摄取和 megalin 的表达。
Front Immunol. 2023 Sep 1;14:1260973. doi: 10.3389/fimmu.2023.1260973. eCollection 2023.
6
Modeling fibrotic alveolar transitional cells with pluripotent stem cell-derived alveolar organoids.用多能干细胞衍生的肺泡类器官模拟肺纤维化的肺泡上皮细胞转分化。
Life Sci Alliance. 2023 May 25;6(8). doi: 10.26508/lsa.202201853. Print 2023 Aug.
7
GSK3 inhibition rescues growth and telomere dysfunction in dyskeratosis congenita iPSC-derived type II alveolar epithelial cells.GSK3 抑制可挽救先天性角化不良症 iPSC 来源的 II 型肺泡上皮细胞的生长和端粒功能障碍。
Elife. 2022 May 13;11:e64430. doi: 10.7554/eLife.64430.
8
A New Homotetramer Hemoglobin in the Pulmonary Surfactant of Plateau Zokors ().高原鼢鼠肺表面活性物质中的一种新型同源四聚体血红蛋白( ) 。 (注:原文括号内内容不完整,翻译时保留原样)
Front Genet. 2022 Mar 15;13:824049. doi: 10.3389/fgene.2022.824049. eCollection 2022.
9
Chitin-Derived AVR-48 Prevents Experimental Bronchopulmonary Dysplasia (BPD) and BPD-Associated Pulmonary Hypertension in Newborn Mice.壳聚糖衍生的 AVR-48 可预防新生小鼠实验性支气管肺发育不良(BPD)和 BPD 相关肺动脉高压。
Int J Mol Sci. 2021 Aug 9;22(16):8547. doi: 10.3390/ijms22168547.
10
Isolation and culture of mouse alveolar type II cells to study type II to type I cell differentiation.分离和培养小鼠肺泡 II 型细胞以研究 II 型细胞向 I 型细胞的分化。
STAR Protoc. 2020 Dec 31;2(1):100241. doi: 10.1016/j.xpro.2020.100241. eCollection 2021 Mar 19.