human hff1  (ATCC)

Journal: iScience

Article Title: Enhanced cell contact and planarian tissue extract increase DNA replication and viability for neoblast cultivation

doi: 10.1016/j.isci.2026.115274

Figure Lengend Snippet: The feeder cell layer promotes DNA replication in neoblasts (A) Schematic diagram and representative images showing SiRNeoblasts seeded on HFF1 and MEF feeder layer, respectively. Scale bars, 50 μm. (B) Cell morphology of SiRNeoblasts cultured on HFF1 or MEF feeder layer for 1, 3, and 7 days. Scale bars, 50 μm. (C) Relative F-ara-EdU + cell ratio of SiRNeoblasts cultured in the plastic flat plate, HFF1, and MEF feeder layer conditions for 3 days. Three wells were assayed in each group. Data are represented as mean ± SEM. Binomial GLM calculates p values. ∗∗∗∗ p < 0.0001. The ratio was calculated as (total number of F-ara-EdU + cells)/(initial number of seeded cells). (D) Heatmap shows expression of genes related to nucleoside metabolism in cells without culture or cells cultured in the plastic flat plate, HFF1, and MEF feeder layer conditions for 1 day. Each group contains three replicates. See also , , and .

Article Snippet: Human: HFF1 , ATCC , SCRC-1041.

Techniques: Cell Culture, Expressing

Journal: iScience

Article Title: Enhanced cell contact and planarian tissue extract increase DNA replication and viability for neoblast cultivation

doi: 10.1016/j.isci.2026.115274

Figure Lengend Snippet: Planarian extract improves cell viability (A and B) Relative PI + dead cell ratio of SiRNeoblasts cultured in the plastic flat plate, the U-bottom plate, HFF1, and MEF feeder layer conditions for 3 days (A) and 7 days (B), respectively. Three wells were assayed in each group. Data are represented as mean ± SEM. All other experimental groups were compared to the plastic flat plate group to assess statistical significance. One-way ANOVA with the Tukey test calculates adjusted p values. ∗∗0.001 < p < 0.01, ∗∗∗∗ p < 0.0001. n.s., no significance. (C) Workflow of preparing planarian extract. (D) Relative PI + dead cell ratio of SiRNeoblasts cultured for 1 and 3 days under five conditions. These five conditions include the plastic flat plate with or without planarian extract, the U-bottom plate with or without planarian extract, and HFF1 feeder layer. Three wells were assayed in each group. Data are represented as mean ± SEM. One-way ANOVA with the Tukey test calculates adjusted p values. ∗0.01 < p < 0.05, ∗∗0.001 < p < 0.01, ∗∗∗0.0001 < p < 0.001. n.s., no significance. (E) Relative F-ara-EdU + cell ratio of SiRNeoblasts cultured for 1 day under five conditions. Three wells were assayed in each group. Data are represented as mean ± SEM. Binomial GLM calculates p values. ∗∗∗∗ p < 0.0001. The ratio was calculated as (total number of F-ara-EdU + cells)/(initial number of seeded cells). (F) Relative piwi-1 + cell ratio of SiRNeoblasts cultured for 7 days under six conditions. The differences among these six conditions lie in three factors: aggregate formation, the addition of extract or not, and the duration of extract exposure. Three wells were assayed in each group. Data are represented as mean ± SEM. One-way ANOVA with the Tukey test calculates adjusted p values. ∗0.01 < p < 0.05, ∗∗0.001 < p < 0.01, n.s., no significance. The ratio was calculated as (total number of piwi-1 + cells)/(initial number of seeded cells). (G) Relative dead cell ratio of SiRNeoblasts cultured for 7 days under six conditions. Three wells were assayed in each group. Data are represented as mean ± SEM. One-way ANOVA with the Tukey test calculates adjusted p values. ∗0.01 < p < 0.05, ∗∗∗0.0001 < p < 0.001, ∗∗∗∗ p < 0.0001. See also .

Article Snippet: Human: HFF1 , ATCC , SCRC-1041.

Techniques: Cell Culture

Journal: BMC Microbiology

Article Title: First human cell-based cultivation system for the syphilis spirochete Treponema pallidum

doi: 10.1186/s12866-026-04856-5

Figure Lengend Snippet: Human foreskin fibroblast cell lines support the growth of T. pallidum in vitro . A Human foreskin fibroblast cell lines (MoNa, HFF1, and HFFC) support the growth of T. pallidum in long-term, continuous, in vitro cultivation. While cultivation of strain SS14 was discontinued after 10 weeks, in vitro cultures of the DAL-1 strain have been ongoing for over one year. During this period, scheme of subcultures was optimized (up to 1:20). A booster passage (*), extending the standard 7-day subculture to a 14-day period with a cultivation medium exchange on day 7, was employed to enrich the treponemal culture during critical declines. In vitro cultivation was performed in triplicate (i.e., in three cultivation wells) and the mean values for each subculture are presented in graph. Source data from individual wells are shown in Supplementary Table . B Parallel cultivation for seven days ( n = 15) with defined DAL-1 inoculum (10 6 treponemes) validated the differences in growth support of individual foreskin cell lines. Treponemal growth on human foreskin fibroblast cells was slower compared to growth on rabbit epithelial Sf1Ep cells. Red bar, mean. C Human foreskin-based cultivation system supports the growth of various T. pallidum strains ( n = 8), from the Nichols-like as well as the SS14-like cluster. Note that human foreskin fibroblast cells were prepared as an equal mixture of three tested cell lines. Each T. pallidum strain was cultivated in a single in vitro well, representing a sole experimental replicate used for data acquisition

Article Snippet: Human foreskin fibroblasts HFF1 (SCRC-1041; ATCC) and HFFC (300715; Cytion) were purchased, while the third cell line (MoNa) was kindly provided by Dr. Vladimir Rotrekl (Masaryk University), and was originally obtained from the National Tissue Centre (Czech Republic).

Techniques: In Vitro

Journal: Alzheimer's & Dementia

Article Title: Interconnections of insulin/IGF‐1 signaling and autophagy abnormalities in Alzheimer's disease

doi: 10.1002/alz.70099

Figure Lengend Snippet: Measuring endocytic and autophagic factors by FICC. A, Schematic of endocytosis (red markers) and autophagy (green markers). B, C, Images from light microscopy (B, upper panels) and corresponding CellProfiler (B, lower panels), or confocal microscopy (C) in HFF1 cells. Images show LC3 and LAMP2 in green and RAB5 and RAB7 in red fluorescence for four different combinations: LC3/RAB5, LC3/RAB7, LAMP2/RAB5, and LAMP2/RAB7. Nuclei were counterstained with DAPI. The insets in (C) depict magnifications from YZ or XZ planes as indicated. Size bars: 5 µm in (B), 20 µm in (C). For visualization purposes, the colors in the CellProfiler images (B) have been amplified. D, CellProfiler data on speckles counts per area and sizes for LC3, LAMP2, RAB5, and RAB7 for naïve AD, OC, and YC cells. Data are from 200 cells per group. One‐way analysis of variance with Sǐdák multiple comparisons was used for group comparisons depicting ns < 0.1; * P < 0.05; ** P < 0.01; *** P < 0.001. AD, late‐onset Alzheimer's disease patient; HFF1, human foreskin fibroblast 1; FICC, fluorescence immunocytochemistry; LAMP2, lysosomal associated membrane protein 2; LC3, microtubule‐associated proteins 1A/1B light chain 3; LOAD, late‐onset Alzheimer's disease; OC, non‐demented age‐matched control; RAB5, Ras related protein 5; RAB7, Ras related protein 7; YC, healthy young control.

Article Snippet: The human foreskin fibroblast 1 (HFF1) cell line was purchased from the American Type Culture Collection (SCRC‐1041).

Techniques: Light Microscopy, Confocal Microscopy, Fluorescence, Amplification, Immunocytochemistry, Membrane, Control