Product Overview

IPF (Idiopathic Pulmonary Fibrosis) is a fatal disease that usually affects adults between the ages of 50-70. The disease is characterized by progressive decline in lung function resulting from scarring of lung tissue.

IPF varies from person to person where in some, fibrosis happens quickly, while the process can be much slower in others. IPF has no cure yet and both geneticand environmental factors are attributed to the development of the disease. Genetics may play a role in causing IPF, and cigarette smoking is the most accepted risk factor in increasing the chances of developing IPF. Recent research has helped doctors understand the disease more closely so they can more quickly diagnose it than in the past. Efforts are still underway in the research community to understand the pathways of disease progression and subsequently develop cures for IPF. IPF was once thought to be a chronic inflammatory process but recent evidence suggests that the abnormal activation of alveolar epithelial cells (AECs) induce over-activation of fibrotic response. The fibroblast and myofibroblast foci secrete excessive amounts of collagens, leading to scarringand destruction of the lung architecture. The mechanisms that link IPF with ageing and aberrant epithelial activation are unknown.

To understand the progression of IPF disease, Lonza offers cryopreserved lung fibroblasts isolated from donors diagnosed with IPF. Cryopreserved IPF fibroblasts are shipped at passage 2 and stain negative for von Willebrand factor VIII, cytokeratins 14, 18 and 19, and alpha smooth muscle actin. All cells test negative for mycoplasma, bacteria, yeast, and fungi. HIV-1, hepatitis B and hepatitis C are not detected for all donors and/or cell lots. A Certificate of Analysis is provided for each cell lot purchased.

Relevant Downloads (Lonza's Normal Human Lung Fibroblasts for IPF Research):

• Lung Epithelium Overexpressed Noncoding RNA (LEON): Role of a Novel Long Intergenic Noncoding RNA in Idiopathic Pulmonary Fibrosis

• The IL-33/ST2 Axis Is Upregulated in Fibrotic Lung Disease

• Extracellular Matrix Metalloproteinase Inducer (EMMPRIN) promotes lung fibroblast proliferation, survival and differentiation to myofibroblasts

Benefits

• Gene expression pathways   

• Phenotypic changes to compounds   

• Transfect diseased cells   

• Co-culture with immune cells   

• Airway remodeling studies   

• Cellular interaction

Content

1 x Cryopreserved ampule of DHLF-IPF containing ≥500,000 cells

Recommended Medium

Lonza FGM™-2 Fibroblast Growth Medium-2 BulletKit™

Catalog #: CC-7231

Please email us at cs@medikonia.com for any enquiry. To place an order, please include the catalog number(s) of the product(s) in the email.

Technical Instructions for culturing Clonetics™ Human Fibroblasts Cells

Reference guidefor human and animal cells from normal to diseased, fresh and cryopreserved