Human Pulmonary Fibroblasts (HPF, Idiopathic Pulmonary Fibrosis)

SKU: 10HU-240

Human Pulmonary Fibroblasts (HPF, Idiopathic Pulmonary Fibrosis)

SKU: 10HU-240
Pricing Starting at

Starting at: $986.00

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10HU-240-0.5MCryopreserved, 0.5 million cells/vialStarting at: $986.00

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Description

Product Description

Fibroblasts, one of the most abundant cell types, are morphologically and functionally heterogeneous [1]. Human pulmonary fibroblasts (HPF) play an important role in maintaining the structural integrity of connective tissue and in the synthesis of extracellular matrix proteins such as collagens and glycoproteins [2]. Under pathological conditions, such as tissue injury, HPF are stimulated to take part in the process of airway inflammation and airway remodeling which might directly or indirectly lead to angiogenesis, idiopathic fibrosis or even cancer [3]. Idiopathic pulmonary fibrosis (IPF) is a rare, progressive illness of the respiratory system, characterized by replacement of healthy lung tissue with altered extracellular matrix and alveolar architecture is destroyed. IPF is believed to be the result of an aberrant wound healing process involving abnormal fibroblasts activation [4].

iXCells Biotechnologies provides high quality HPF, which are isolated from lung tissue of IPF patients. It provides a robust model for in vitro studies of IPF as well as other fibroblasts related diseases. HPF from iXCells Biotechnologies are cryopreserved at P2, with >0.5 million cells in each vial. HPF express Fibronectin and Vimentin. They are negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast, and fungi and can further expand for 10 population doublings in Fibroblast Growth Medium (Cat# MD-0011) under the condition suggested by iXCells Biotechnologies.

 

Figure 1. Human Pulmonary Fibroblasts (HPF, Idiopathic Pulmonary Fibrosis). The cells were recovered, and seeded at 10,000 cells/cm2 following iXCells’ protocol. Phase contrast images were taken at the indicated time post recovery.

 

Figure 2. Immunofluorescence staining of Human Pulmonary Fibroblasts (HPF, Idiopathic Pulmonary Fibrosis) with antibodies against Fibronectin (Red) and Vimentin (Green). Nuclei were counterstained by DAPI (Blue).

 

Product Details

Tissue Human lung tissue
Package Size 0.5 million cells/vial
Passage Number P2
Shipped Cryopreserved
Storage Liquid nitrogen
Growth Properties Adherent
Media Fibroblast Growth Medium(Cat# MD-0011)

 

Download Datasheet

Download Datasheet

  • [1] Yang P, Luo Q, Wang X, Fang Q, Fu Z, Li J, Lai Y, Chen X, Xu X, Peng X, Hu K, Nie X, Liu S, Zhang J, Li J, Shen C, Gu Y, Liu J, Chen J, Zhong N, Su J. Comprehensive Analysis of Fibroblast Activation Protein Expression in Interstitial Lung Diseases. Am J Respir Crit Care Med. 2023 Jan 15;207(2):160-172.
  • [2] Hu X, Xu Q, Wan H, Hu Y, Xing S, Yang H, Gao Y, He Z. PI3K-Akt-mTOR/PFKFB3 pathway mediated lung fibroblast aerobic glycolysis and collagen synthesis in lipopolysaccharide-induced pulmonary fibrosis. Lab Invest. 2020 Jun;100(6):801-811. doi: 10.1038/s41374-020-0404-9. Epub 2020 Feb 12.
  • [3] Cruz-Bermúdez A, Laza-Briviesca R, Vicente-Blanco RJ, García-Grande A, Coronado MJ, Laine-Menéndez S, Alfaro C, Sanchez JC, Franco F, Calvo V, Romero A, Martin-Acosta P, Salas C, Garcia JM, Provencio M. Cancer-associated fibroblasts modify lung cancer metabolism involving ROS and TGF-β signaling. Free Radic Biol Med. 2019 Jan;130:163-173. doi: 10.1016/j.freeradbiomed.2018.10.450. Epub 2018 Nov 1.
  • [4] Richeldi L, Collard HR, Jones MG. Idiopathic pulmonary fibrosis. Lancet. 2017 May 13;389(10082):1941-1952. doi: 10.1016/S0140-6736(17)30866-8. Epub 2017 Mar 30.

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