Immortalized Human Fetal Osteoblast-SV40

Cat.No.: CSC-I9021L

Species: Homo sapiens

Source: Bone

Morphology: polygonal

Culture Properties: Adherent

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Cat.No.
CSC-I9021L
Description
Species
Homo sapiens
Source
Bone
Culture Properties
Adherent
Morphology
polygonal
Immortalization Method
Conditionally immortalized with a temperature-sensitive(ts) mutant, tsA58, by serial passaging and transduction with lentiviruses carrying SV40 large T antigen
Application
For Research Use Only
Storage
Directly and immediately transfer cells from dry ice to liquid nitrogen upon receiving and keep the cells in liquid nitrogen until cell culture needed for experiments.

Note: Never can cells be kept at -20 °C.
Shipping
Dry Ice.
Recommended Products
CSC-C4032X Human Osteoblasts (HOB)
CIK-HT003 HT® Lenti-SV40T Immortalization Kit
Quality Control
Real Time PCR was used to quantify SV40 gene expression in immortalized cell line.
BioSafety Level
II
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Immortalized Human Fetal Osteoblast‑SV40 (hFOB1.19‑SV40) cells are human osteoblastic cells immortalized with the SV40 large T antigen. These cells were originally derived from fetal human bone and provide a conditionally proliferative osteoblastic cell line. The parental hFOB1.19 cell line was immortalized through transfection with the SV40 T antigen which is temperature sensitive to allow for proliferation while maintaining osteoblastic phenotypic characteristics (Keller et al., 1994). Primary osteoblasts isolated from tissues can only survive for a limited amount of time in vitro. Therefore, immortalized cells like hFOB1.19 cells allow for a more robust and reproducible osteoblastic model system.

The hFOB1.19‑SV40 cells are polygonal in shape with a fibroblast-like morphology and grow as adherent monolayers. They express osteoblast specific markers such as alkaline phosphatase (ALP), osteocalcin, bone sialoprotein and type I collagen, further confirming osteoblastic characteristics. When treated with differentiation media containing ascorbic acid and β‑glycerophosphate cells treated showed increased ALP activity and mineralization of the matrix, indicating the cells maintain osteogenic differentiation potential.

Immortalized human fetal osteoblast cells have been used to study osteoblast proliferation and differentiation, regulation of the extracellular matrix, mechanotransduction, evaluation of biomaterials, drug screening assays, bone remodeling as well as response to hormonal regulation such as vitamin D and parathyroid hormone.

Human Fetal Osteoblast Cells (hFOB) form Solid Spheroids under Proliferative Conditions in the Absence of a Necrotic Core

Skeletal bone function depends on cells and their niches, which together regulate differentiation and remodeling. Here, Marozin et al. present an in vitro 3D model using human fetal osteoblasts (hFOB 1.19) to study osteocyte commitment and examine effects of biomaterials or substances on these processes.

hFOB 1.19 cells form spheroids in non-adherent 3D culture. Histological analysis showed spheroids grown >30 days under proliferative conditions exhibited no necrosis (Fig. 1A), confirmed across osteogenic and adipo-inductive conditions. Proliferative spheroids continued growing, while induction media caused growth arrest and nuclear fragmentation (Fig. 1B). Adipogenesis-induced spheroids were small with irregular boundaries and unstructured appearance, lacking shell-core distinction. Osteogenesis-induced spheroids showed minimal growth and smaller size than growth medium controls, with H&E staining revealing a basophilic environment and no necrotic cores. Growth medium spheroids displayed strong eosinophilic staining compared to induction media. Sirius red staining for collagen visualization (Fig. 1C) showed structured extracellular matrix throughout growth medium spheroids, with highest density in central regions. Osteogenic spheroids exhibited ring-shaped, concentric matrix layers between deep shell cells, while adipogenic spheroids showed no characteristic collagen staining.

hFOB spheroid development under proliferative, osteo- and adipo-inductive conditions.

Fig. 1. hFOB spheroid development under proliferative, osteo- and adipo-inductive conditions (Marozin S, Simon-Nobbe B, et al., 2024).

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