Posts Tagged ‘EDTA’

Curator, Reporter: Aviral Vatsa, PhD, MBBS

Isolation of primary osteocytes from skeletally mature mice bones: A report on “Isolation and culture of primary osteocytes from the long bones of skeletally mature and aged mice” (BioTechniques 52:361-373 ( June 2012) doi 10.2144/0000113876)

A new study by Stern et al reports a technique where in the authors have isolated primary osteocytes from mature and aged mice.

Osteocytes are deeply embedded in the mineralised matrix of bone. They form the majority cell types of bone and play vital function in maintenance of bone homeostasis. However their study has been limited by their location in the bone and that they are terminally differentiated cells.

Osteocytes are the most abundant of the three bone cell types; however, the least is known about them. While their location deep within the bone matrix makes them ideally situated to sense bone strain, it also makes their observation and study in vivo difficult. Additionally, primary osteocytes, particularly those within the long bones of skeletally mature animals, have proven difficult to obtain and study ex vivo. Furthermore, once primary osteocytes are obtained, their study is often limited by their inability to proliferate as they are considered terminally differentiated cells. ”

As a result majority of the studies on osteocytes in vitro have used either cell lines and/or primary cells from new-born animals such as chicken, rat and mouse.

The MLO-Y4 cell line is well-characterized and represents the phenotype of early osteocytes ”

“Although the MLO-Y4 cell line is a very powerful tool for the study of osteocytes in vitro, there are known differences between primary osteocytes and the immortalized MLO-Y4 cell line. For example, MLO-Y4 cells express low to undetectable levels of Dentin matrix protein 1 (Dmp1) and Sclerostin (Sost), while osteocytes are known to express these genes in vivo .”

Primary osteocytes have most commonly been isolated from 16- or 18-day-old chick calvaria or from newborn through 4-day-old rat calvaria, 12-day-old mouse calvaria, and 3- to 4-week-old mouse calvaria and long bones.”

Studies utilizing these primary osteocytes can provide insight to the behavior of osteocytes during development but do not aid in the study of osteocytes from skeletally mature animals or enable the comparison between osteocytes isolated from skeletally mature but relatively young mice (4- to 6-month) and aged mice (>22-month-old).”

To circumvent the above mentioned limitations the authors utilised multi-step digestion technique. They subjected mouse long bone pieces (from 4-month old mouse and 22-month old mouse) to collagenase and EDTA alternatively for 25 minutes and collected the aspirate after each step for plating and culture of cells. (as described in the table, which has been taken from the study).

Table 1. Osteocyte isolation from murine long bone (courtesy: Stern et al)

They collected cells from nine such alternate steps in total and also the left over bone. These cells were then cultured for 7 days. Following parameters were tested to characterise the osteocytes.

  • E11/GP38 staining – early osteocyte specific protein
  • Alkaline Phosphatase (ALP) staining – indicator of osteoblastic state
  • COL 1 – major component of bone and produced by osteoblasts
  • Gene expression of E11, SOST, MEPE, Dmp1 – markers of osteogencity in different stages of osteogenesis
    • Osteoid osteocytes are known to express E11, Phex, and Mepe, while mineralizing osteocytes express Dmp1, and mature osteocytes encased in a mineralized matrix express Sost and Fgf23”

The authors were able to demonstrate that the isolated cells indeed expressed osteogenic markers. It was observed that cells isolated from later digestion steps (6-9) were more osteocyte like. This was also the case with the cells isolated from the left over bone pieces.

In this study, we were able to success fully isolate primary cells displaying several characteristics of osteocytes from the long bones of skeletally mature 4-month-old and 22-month-old mice through a process of sequential digestions and the use of a tissue homogenizer. From both the 4-month-old and 22-month-old mice, approximately 250,000 cells per osteocyte-enriched digestion (digestions 7–9) were obtained. These cells expressed E11/GP38 protein, and they lacked ALP and COL1A1 expression found in osteoblasts. Furthermore, several genes known to be expressed in osteocytes were also expressed in the cells obtained using our methodology. These include E11/gp38, Sost, Cox2, Mepe, Phex, and Dmp1.”


As the authors pointed out, their study characterised the cells ensemble from separate digestion steps. This could lead to having a mixed population from each step.

The authors did not mention about the proliferation (or the absence of it) of the isolated cells. Since osteocytes are terminally differentiated cells, theoretically they should not proliferate. In addition when such primary cells are co-cultured with dividing cells, such as osteoblasts and fibroblasts in this case, the dividing population tends to over grow in culture leaving behind very few primary osteocytes. A detailed characterisation of these cells at different stages of digestion along with progressive time points will be very helpful.


As authors claim, in future, this technique can help scientists to answer tricky questions about osteocytes such as comparing osteocytes from animals grouped on the basis of age, disease, bone characteristics, and therapies.

Reference: Isolation and culture of primary osteocytes from the long bones of skeletally mature and aged mice. BioTechniques 52:361-373 ( June 2012) doi 10.2144/0000113876 .

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