Comparison of FRPE and human embryonic stem cell-derived RPE behavior on aged human Bruch's membrane

Invest Ophthalmol Vis Sci. 2011 Jul 1;52(8):4979-97. doi: 10.1167/iovs.10-5386.

Abstract

Purpose: To compare RPE derived from human embryonic stem cells (hES-RPE) and fetal RPE (fRPE) behavior on human Bruch's membrane (BM) from aged and AMD donors.

Methods: hES-RPE of 3 degrees of pigmentation and fRPE were cultured on BM explants. Explants were assessed by light, confocal, and scanning electron microscopy. Integrin mRNA levels were determined by real-time polymerase chain reaction studies. Secreted proteins in media were analyzed by multiplex protein analysis after 48-hour exposure at culture day 21.

Results: hES-RPE showed impaired initial attachment compared to fRPE; pigmented hES-RPE showed nuclear densities similar to fRPE at day 21. At days 3 and 7, hES-RPE resurfaced BM to a limited degree, showed little proliferation (Ki-67), and partial retention of RPE markers (MITF, cytokeratin, and CRALBP). TUNEL-positive nuclei were abundant at day 3. fRPE exhibited substantial BM resurfacing at day 3 with decreased resurfacing at later times. Most fRPE retained RPE markers. Ki-67-positive nuclei decreased with time in culture. TUNEL staining was variable. Increased integrin mRNA expression did not appear to affect cell survival at day 21. hES-RPE and fRPE protein secretion was similar on equatorial BM except for higher levels of nerve growth factor and thrombospondin-2 (TSP2) by hES-RPE. On submacular BM, fRPE secreted more vascular endothelial growth factor (VEGF), brain-derived neurotrophic factor, and platelet-derived growth factor; hES-RPE secreted more TSP2.

Conclusions: Although pigmented hES-RPE and fRPE resurfaced aged and AMD BM to a similar, limited degree at day 21, cell behavior at earlier times was markedly dissimilar. Differences in protein secretion may indicate that hES-RPE may not function identically to native RPE after seeding on aged or AMD BM.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Aging / physiology*
  • Bruch Membrane / cytology*
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cells, Cultured
  • Embryonic Stem Cells / cytology*
  • Female
  • Fetal Stem Cells / cytology*
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • In Situ Nick-End Labeling
  • Integrins / genetics
  • Keratins / metabolism
  • Ki-67 Antigen / genetics
  • Ki-67 Antigen / metabolism
  • Macular Degeneration / pathology
  • Male
  • Microphthalmia-Associated Transcription Factor / genetics
  • Microphthalmia-Associated Transcription Factor / metabolism
  • Microscopy, Confocal
  • Microscopy, Electron, Scanning
  • Middle Aged
  • Organ Culture Techniques
  • RNA, Messenger / metabolism
  • Retinal Pigment Epithelium / cytology*
  • Retinal Pigment Epithelium / physiology
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • 11-cis-retinal-binding protein
  • Carrier Proteins
  • Integrins
  • Ki-67 Antigen
  • MITF protein, human
  • Microphthalmia-Associated Transcription Factor
  • RNA, Messenger
  • Keratins